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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:HLA-B-HLA-B (FusionGDB2 ID:36491)

Fusion Gene Summary for HLA-B-HLA-B

check button Fusion gene summary
Fusion gene informationFusion gene name: HLA-B-HLA-B
Fusion gene ID: 36491
HgeneTgene
Gene symbol

HLA-B

HLA-B

Gene ID

3106

3106

Gene namemajor histocompatibility complex, class I, Bmajor histocompatibility complex, class I, B
SynonymsAS|B-4901|HLABAS|B-4901|HLAB
Cytomap

6p21.33

6p21.33

Type of geneprotein-codingprotein-coding
Descriptionmajor histocompatibility complex, class I, BHLA class I antigen HLA-BHLA class I histocompatibility antigen, B alpha chainMHC HLA-B cell surface glycoproteinMHC HLA-B transmembrane glycoproteinMHC class 1 antigenMHC class I antigen HLA-B alpha chainmajor histocompatibility complex, class I, BHLA class I antigen HLA-BHLA class I histocompatibility antigen, B alpha chainMHC HLA-B cell surface glycoproteinMHC HLA-B transmembrane glycoproteinMHC class 1 antigenMHC class I antigen HLA-B alpha chain
Modification date2020032220200322
UniProtAcc

P01889

P01889

Ensembl transtripts involved in fusion geneENST00000412585, ENST00000425848, 
ENST00000450871, ENST00000359635, 
ENST00000435618, ENST00000421349, 
ENST00000412585, ENST00000425848, 
ENST00000450871, ENST00000359635, 
ENST00000435618, ENST00000421349, 
Fusion gene scores* DoF score21 X 13 X 8=21847 X 10 X 1=70
# samples 2410
** MAII scorelog2(24/2184*10)=-3.18586654531133
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/70*10)=0.514573172829758
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: HLA-B [Title/Abstract] AND HLA-B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHLA-B(31321845)-HLA-B(31321934), # samples:1
HLA-B(31321804)-HLA-B(31322303), # samples:1
HLA-B(31322297)-HLA-B(31321909), # samples:1
HLA-B(31322936)-HLA-B(31324524), # samples:1
Anticipated loss of major functional domain due to fusion event.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneHLA-B

GO:0002486

antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent

22031944

HgeneHLA-B

GO:0042270

protection from natural killer cell mediated cytotoxicity

2784569|8046333

TgeneHLA-B

GO:0002486

antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent

22031944

TgeneHLA-B

GO:0042270

protection from natural killer cell mediated cytotoxicity

2784569|8046333


check buttonFusion gene breakpoints across HLA-B (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across HLA-B (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/AAA826150HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
ChiTaRS5.0N/AAW405998HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
ChiTaRS5.0N/ABF909066HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
ChiTaRS5.0N/ACA431962HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-


Top

Fusion Gene ORF analysis for HLA-B-HLA-B

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3UTRENST00000412585ENST00000412585HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000412585ENST00000425848HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000412585ENST00000450871HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000412585ENST00000359635HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000412585ENST00000435618HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000412585ENST00000421349HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-3UTRENST00000425848ENST00000412585HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000425848ENST00000425848HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000425848ENST00000450871HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000425848ENST00000359635HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000425848ENST00000435618HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000425848ENST00000421349HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-3UTRENST00000450871ENST00000412585HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000450871ENST00000425848HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000450871ENST00000450871HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000450871ENST00000359635HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000450871ENST00000435618HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000450871ENST00000421349HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-3UTRENST00000359635ENST00000412585HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000359635ENST00000425848HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000359635ENST00000450871HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000359635ENST00000359635HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000359635ENST00000435618HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000359635ENST00000421349HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-3UTRENST00000435618ENST00000412585HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000435618ENST00000425848HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000435618ENST00000450871HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000435618ENST00000359635HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000435618ENST00000435618HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000435618ENST00000421349HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-3UTRENST00000421349ENST00000412585HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000421349ENST00000425848HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000421349ENST00000450871HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000421349ENST00000359635HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000421349ENST00000435618HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-intronENST00000421349ENST00000421349HLA-Bchr6

31321845

+HLA-Bchr6

31321934

-
intron-3CDSENST00000412585ENST00000412585HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000412585ENST00000425848HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000412585ENST00000450871HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000412585ENST00000359635HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000412585ENST00000435618HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000412585ENST00000421349HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-3CDSENST00000425848ENST00000412585HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000425848ENST00000425848HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000425848ENST00000450871HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000425848ENST00000359635HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000425848ENST00000435618HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000425848ENST00000421349HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-3CDSENST00000450871ENST00000412585HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000450871ENST00000425848HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000450871ENST00000450871HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000450871ENST00000359635HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000450871ENST00000435618HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000450871ENST00000421349HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-3CDSENST00000359635ENST00000412585HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000359635ENST00000425848HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000359635ENST00000450871HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000359635ENST00000359635HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000359635ENST00000435618HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000359635ENST00000421349HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-3CDSENST00000435618ENST00000412585HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000435618ENST00000425848HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000435618ENST00000450871HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000435618ENST00000359635HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000435618ENST00000435618HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000435618ENST00000421349HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-3CDSENST00000421349ENST00000412585HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000421349ENST00000425848HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000421349ENST00000450871HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000421349ENST00000359635HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000421349ENST00000435618HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-intronENST00000421349ENST00000421349HLA-Bchr6

31321804

+HLA-Bchr6

31322303

-
intron-3UTRENST00000412585ENST00000412585HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000412585ENST00000425848HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000412585ENST00000450871HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000412585ENST00000359635HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000412585ENST00000435618HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000412585ENST00000421349HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-3UTRENST00000425848ENST00000412585HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000425848ENST00000425848HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000425848ENST00000450871HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000425848ENST00000359635HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000425848ENST00000435618HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000425848ENST00000421349HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-3UTRENST00000450871ENST00000412585HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000450871ENST00000425848HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000450871ENST00000450871HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000450871ENST00000359635HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000450871ENST00000435618HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000450871ENST00000421349HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-3UTRENST00000359635ENST00000412585HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000359635ENST00000425848HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000359635ENST00000450871HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000359635ENST00000359635HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000359635ENST00000435618HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000359635ENST00000421349HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-3UTRENST00000435618ENST00000412585HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000435618ENST00000425848HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000435618ENST00000450871HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000435618ENST00000359635HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000435618ENST00000435618HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000435618ENST00000421349HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-3UTRENST00000421349ENST00000412585HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000421349ENST00000425848HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000421349ENST00000450871HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000421349ENST00000359635HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000421349ENST00000435618HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-intronENST00000421349ENST00000421349HLA-Bchr6

31322297

+HLA-Bchr6

31321909

-
intron-3CDSENST00000412585ENST00000412585HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000412585ENST00000425848HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000412585ENST00000450871HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000412585ENST00000359635HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000412585ENST00000435618HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000412585ENST00000421349HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-3CDSENST00000425848ENST00000412585HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000425848ENST00000425848HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000425848ENST00000450871HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000425848ENST00000359635HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000425848ENST00000435618HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000425848ENST00000421349HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-3CDSENST00000450871ENST00000412585HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000450871ENST00000425848HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000450871ENST00000450871HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000450871ENST00000359635HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000450871ENST00000435618HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000450871ENST00000421349HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-3CDSENST00000359635ENST00000412585HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000359635ENST00000425848HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000359635ENST00000450871HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000359635ENST00000359635HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000359635ENST00000435618HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000359635ENST00000421349HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-3CDSENST00000435618ENST00000412585HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000435618ENST00000425848HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000435618ENST00000450871HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000435618ENST00000359635HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000435618ENST00000435618HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000435618ENST00000421349HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-3CDSENST00000421349ENST00000412585HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000421349ENST00000425848HLA-Bchr6

31322936

+HLA-Bchr6

31324524

-
intron-intronENST00000421349ENST00000450871HLA-Bchr6

31322936

+HLA-Bchr6

31324524

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intron-intronENST00000421349ENST00000359635HLA-Bchr6

31322936

+HLA-Bchr6

31324524

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intron-intronENST00000421349ENST00000435618HLA-Bchr6

31322936

+HLA-Bchr6

31324524

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intron-intronENST00000421349ENST00000421349HLA-Bchr6

31322936

+HLA-Bchr6

31324524

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check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for HLA-B-HLA-B


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for HLA-B-HLA-B


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HLA-B

P01889

HLA-B

P01889

FUNCTION: Antigen-presenting major histocompatibility complex class I (MHCI) molecule. In complex with B2M/beta 2 microglobulin displays primarily viral and tumor-derived peptides on antigen-presenting cells for recognition by alpha-beta T cell receptor (TCR) on HLA-B-restricted CD8-positive T cells, guiding antigen-specific T cell immune response to eliminate infected or transformed cells (PubMed:25808313, PubMed:29531227, PubMed:9620674, PubMed:23209413). May also present self-peptides derived from the signal sequence of secreted or membrane proteins, although T cells specific for these peptides are usually inactivated to prevent autoreactivity (PubMed:7743181, PubMed:18991276). Both the peptide and the MHC molecule are recognized by TCR, the peptide is responsible for the fine specificity of antigen recognition and MHC residues account for the MHC restriction of T cells (PubMed:29531227, PubMed:9620674, PubMed:24600035). Typically presents intracellular peptide antigens of 8 to 13 amino acids that arise from cytosolic proteolysis via constitutive proteasome and IFNG-induced immunoproteasome (PubMed:23209413). Can bind different peptides containing allele-specific binding motifs, which are mainly defined by anchor residues at position 2 and 9 (PubMed:25808313, PubMed:29531227). {ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:23209413, ECO:0000269|PubMed:24600035, ECO:0000269|PubMed:25808313, ECO:0000269|PubMed:29531227, ECO:0000269|PubMed:7743181, ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*07:02: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and mainly a Leu anchor residue at the C-terminus (PubMed:7743181). Presents a long peptide (APRGPHGGAASGL) derived from the cancer-testis antigen CTAG1A/NY-ESO-1, eliciting a polyclonal CD8-positive T cell response against tumor cells (PubMed:29531227). Presents viral epitopes derived from HIV-1 gag-pol (TPQDLNTML) and Nef (RPQVPLRPM) (PubMed:25808313). Presents an immunodominant epitope derived from SARS-CoV-2 N/nucleoprotein (SPRWYFYYL) (PubMed:32887977). Displays self-peptides including a peptide derived from the signal sequence of HLA-DPB1 (APRTVALTA) (PubMed:7743181). {ECO:0000269|PubMed:25808313, ECO:0000269|PubMed:29531227, ECO:0000269|PubMed:32887977, ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*08:01: Presents to CD8-positive T cells viral epitopes derived from EBV/HHV-4 EBNA3 (QAKWRLQTL), eliciting cytotoxic T cell response. {ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*13:02: Presents multiple HIV-1 epitopes derived from gag (RQANFLGKI, GQMREPRGSDI), nef (RQDILDLWI), gag-pol (RQYDQILIE, GQGQWTYQI) and rev (LQLPPLERL), all having in common a Gln residue at position 2 and mainly hydrophobic amino acids Leu, Ile or Val at the C-terminus. Associated with succesful control of HIV-1 infection. {ECO:0000269|PubMed:17251285}.; FUNCTION: Allele B*18:01: Preferentially presents octomeric and nonameric peptides sharing a common motif, namely a Glu at position 2 and Phe or Tyr anchor residues at the C-terminus (PubMed:14978097, PubMed:23749632, PubMed:18991276). Presents an EBV/HHV-4 epitope derived from BZLF1 (SELEIKRY) (PubMed:23749632). May present to CD8-positive T cells an antigenic peptide derived from MAGEA3 (MEVDPIGHLY), triggering an anti-tumor immune response (PubMed:12366779). May display a broad repertoire of self-peptides with a preference for peptides derived from RNA-binding proteins (PubMed:14978097). {ECO:0000269|PubMed:12366779, ECO:0000269|PubMed:14978097, ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:23749632}.; FUNCTION: Allele B*27:05: Presents to CD8-positive T cells immunodominant viral epitopes derived from HCV POLG (ARMILMTHF), HIV-1 gag (KRWIILGLNK), IAV NP (SRYWAIRTR), SARS-CoV-2 N/nucleoprotein (QRNAPRITF), EBV/HHV-4 EBNA4 (HRCQAIRKK) and EBV/HHV-4 EBNA6 (RRIYDLIEL), confering longterm protection against viral infection (PubMed:19139562, PubMed:18385228, PubMed:15113903, PubMed:9620674, PubMed:32887977). Can present self-peptides derived from cytosolic and nuclear proteins. All peptides carry an Arg at position 2 (PubMed:1922338). The peptide-bound form interacts with NK cell inhibitory receptor KIR3DL1 and inhibits NK cell activation in a peptide-specific way, being particularly sensitive to the nature of the amino acid side chain at position 8 of the antigenic peptide (PubMed:8879234, PubMed:15657948). KIR3DL1 fails to recognize HLA-B*27:05 in complex with B2M and EBV/HHV-4 EBNA6 (RRIYDLIEL) peptide, which can lead to increased activation of NK cells during infection (PubMed:15657948). May present an altered repertoire of peptides in the absence of TAP1-TAP2 and TAPBPL (PubMed:9620674). {ECO:0000269|PubMed:15113903, ECO:0000269|PubMed:15657948, ECO:0000269|PubMed:18385228, ECO:0000269|PubMed:19139562, ECO:0000269|PubMed:1922338, ECO:0000269|PubMed:8879234, ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*40:01: Presents immunodominant viral epitopes derived from EBV/HHV-4 LMP2 (IEDPPFNSL) and SARS-CoV-2 N/nucleoprotein (MEVTPSGTWL), triggering memory CD8-positive T cell response (PubMed:18991276, PubMed:32887977). Displays self-peptides sharing a signature motif, namely a Glu at position 2 and a Leu anchor residue at the C-terminus (PubMed:18991276). {ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:32887977}.; FUNCTION: Allele B*41:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ala or Pro anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*44:02: Presents immunodominant viral epitopes derived from EBV/HHV-4 EBNA4 (VEITPYKPTW) and EBNA6 (AEGGVGWRHW, EENLLDFVRF), triggering memory CD8-positive T cell response (PubMed:9620674, PubMed:18991276). Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Phe, Tyr or Trp anchor residues at the C-terminus (PubMed:18991276). {ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*45:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ala or Pro anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*46:01: Preferentially presents nonameric peptides sharing a signature motif, namely Ala and Leu at position 2 and Tyr, Phe, Leu, or Met anchor residues at the C-terminus. The peptide-bound form interacts with KIR2DL3 and inhibits NK cell cytotoxic response in a peptide-specific way. {ECO:0000269|PubMed:28514659}.; FUNCTION: Allele B*47:01: Displays self-peptides sharing a signature motif, namely an Asp at position 2 and Leu or Met anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*49:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ile or Val anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*50:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ala or Pro anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*51:01: Presents an octomeric HIV-1 epitope derived from gag-pol (TAFTIPSI) to the public TRAV17/TRBV7-3 TCR clonotype, strongly suppressing HIV-1 replication. {ECO:0000269|PubMed:24600035}.; FUNCTION: Allele B*54:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Ala anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*55:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Ala anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*56:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Ala anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*57:01: The peptide-bound form recognizes KIR3DL1 and inhibits NK cell cytotoxic response. {ECO:0000269|PubMed:22020283, ECO:0000269|PubMed:25480565}.; FUNCTION: Allele B*67:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Leu anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.FUNCTION: Antigen-presenting major histocompatibility complex class I (MHCI) molecule. In complex with B2M/beta 2 microglobulin displays primarily viral and tumor-derived peptides on antigen-presenting cells for recognition by alpha-beta T cell receptor (TCR) on HLA-B-restricted CD8-positive T cells, guiding antigen-specific T cell immune response to eliminate infected or transformed cells (PubMed:25808313, PubMed:29531227, PubMed:9620674, PubMed:23209413). May also present self-peptides derived from the signal sequence of secreted or membrane proteins, although T cells specific for these peptides are usually inactivated to prevent autoreactivity (PubMed:7743181, PubMed:18991276). Both the peptide and the MHC molecule are recognized by TCR, the peptide is responsible for the fine specificity of antigen recognition and MHC residues account for the MHC restriction of T cells (PubMed:29531227, PubMed:9620674, PubMed:24600035). Typically presents intracellular peptide antigens of 8 to 13 amino acids that arise from cytosolic proteolysis via constitutive proteasome and IFNG-induced immunoproteasome (PubMed:23209413). Can bind different peptides containing allele-specific binding motifs, which are mainly defined by anchor residues at position 2 and 9 (PubMed:25808313, PubMed:29531227). {ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:23209413, ECO:0000269|PubMed:24600035, ECO:0000269|PubMed:25808313, ECO:0000269|PubMed:29531227, ECO:0000269|PubMed:7743181, ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*07:02: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and mainly a Leu anchor residue at the C-terminus (PubMed:7743181). Presents a long peptide (APRGPHGGAASGL) derived from the cancer-testis antigen CTAG1A/NY-ESO-1, eliciting a polyclonal CD8-positive T cell response against tumor cells (PubMed:29531227). Presents viral epitopes derived from HIV-1 gag-pol (TPQDLNTML) and Nef (RPQVPLRPM) (PubMed:25808313). Presents an immunodominant epitope derived from SARS-CoV-2 N/nucleoprotein (SPRWYFYYL) (PubMed:32887977). Displays self-peptides including a peptide derived from the signal sequence of HLA-DPB1 (APRTVALTA) (PubMed:7743181). {ECO:0000269|PubMed:25808313, ECO:0000269|PubMed:29531227, ECO:0000269|PubMed:32887977, ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*08:01: Presents to CD8-positive T cells viral epitopes derived from EBV/HHV-4 EBNA3 (QAKWRLQTL), eliciting cytotoxic T cell response. {ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*13:02: Presents multiple HIV-1 epitopes derived from gag (RQANFLGKI, GQMREPRGSDI), nef (RQDILDLWI), gag-pol (RQYDQILIE, GQGQWTYQI) and rev (LQLPPLERL), all having in common a Gln residue at position 2 and mainly hydrophobic amino acids Leu, Ile or Val at the C-terminus. Associated with succesful control of HIV-1 infection. {ECO:0000269|PubMed:17251285}.; FUNCTION: Allele B*18:01: Preferentially presents octomeric and nonameric peptides sharing a common motif, namely a Glu at position 2 and Phe or Tyr anchor residues at the C-terminus (PubMed:14978097, PubMed:23749632, PubMed:18991276). Presents an EBV/HHV-4 epitope derived from BZLF1 (SELEIKRY) (PubMed:23749632). May present to CD8-positive T cells an antigenic peptide derived from MAGEA3 (MEVDPIGHLY), triggering an anti-tumor immune response (PubMed:12366779). May display a broad repertoire of self-peptides with a preference for peptides derived from RNA-binding proteins (PubMed:14978097). {ECO:0000269|PubMed:12366779, ECO:0000269|PubMed:14978097, ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:23749632}.; FUNCTION: Allele B*27:05: Presents to CD8-positive T cells immunodominant viral epitopes derived from HCV POLG (ARMILMTHF), HIV-1 gag (KRWIILGLNK), IAV NP (SRYWAIRTR), SARS-CoV-2 N/nucleoprotein (QRNAPRITF), EBV/HHV-4 EBNA4 (HRCQAIRKK) and EBV/HHV-4 EBNA6 (RRIYDLIEL), confering longterm protection against viral infection (PubMed:19139562, PubMed:18385228, PubMed:15113903, PubMed:9620674, PubMed:32887977). Can present self-peptides derived from cytosolic and nuclear proteins. All peptides carry an Arg at position 2 (PubMed:1922338). The peptide-bound form interacts with NK cell inhibitory receptor KIR3DL1 and inhibits NK cell activation in a peptide-specific way, being particularly sensitive to the nature of the amino acid side chain at position 8 of the antigenic peptide (PubMed:8879234, PubMed:15657948). KIR3DL1 fails to recognize HLA-B*27:05 in complex with B2M and EBV/HHV-4 EBNA6 (RRIYDLIEL) peptide, which can lead to increased activation of NK cells during infection (PubMed:15657948). May present an altered repertoire of peptides in the absence of TAP1-TAP2 and TAPBPL (PubMed:9620674). {ECO:0000269|PubMed:15113903, ECO:0000269|PubMed:15657948, ECO:0000269|PubMed:18385228, ECO:0000269|PubMed:19139562, ECO:0000269|PubMed:1922338, ECO:0000269|PubMed:8879234, ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*40:01: Presents immunodominant viral epitopes derived from EBV/HHV-4 LMP2 (IEDPPFNSL) and SARS-CoV-2 N/nucleoprotein (MEVTPSGTWL), triggering memory CD8-positive T cell response (PubMed:18991276, PubMed:32887977). Displays self-peptides sharing a signature motif, namely a Glu at position 2 and a Leu anchor residue at the C-terminus (PubMed:18991276). {ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:32887977}.; FUNCTION: Allele B*41:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ala or Pro anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*44:02: Presents immunodominant viral epitopes derived from EBV/HHV-4 EBNA4 (VEITPYKPTW) and EBNA6 (AEGGVGWRHW, EENLLDFVRF), triggering memory CD8-positive T cell response (PubMed:9620674, PubMed:18991276). Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Phe, Tyr or Trp anchor residues at the C-terminus (PubMed:18991276). {ECO:0000269|PubMed:18991276, ECO:0000269|PubMed:9620674}.; FUNCTION: Allele B*45:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ala or Pro anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*46:01: Preferentially presents nonameric peptides sharing a signature motif, namely Ala and Leu at position 2 and Tyr, Phe, Leu, or Met anchor residues at the C-terminus. The peptide-bound form interacts with KIR2DL3 and inhibits NK cell cytotoxic response in a peptide-specific way. {ECO:0000269|PubMed:28514659}.; FUNCTION: Allele B*47:01: Displays self-peptides sharing a signature motif, namely an Asp at position 2 and Leu or Met anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*49:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ile or Val anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*50:01: Displays self-peptides sharing a signature motif, namely a Glu at position 2 and Ala or Pro anchor residues at the C-terminus. {ECO:0000269|PubMed:18991276}.; FUNCTION: Allele B*51:01: Presents an octomeric HIV-1 epitope derived from gag-pol (TAFTIPSI) to the public TRAV17/TRBV7-3 TCR clonotype, strongly suppressing HIV-1 replication. {ECO:0000269|PubMed:24600035}.; FUNCTION: Allele B*54:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Ala anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*55:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Ala anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*56:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Ala anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.; FUNCTION: Allele B*57:01: The peptide-bound form recognizes KIR3DL1 and inhibits NK cell cytotoxic response. {ECO:0000269|PubMed:22020283, ECO:0000269|PubMed:25480565}.; FUNCTION: Allele B*67:01: Displays peptides sharing a common signature motif, namely a Pro residue at position 2 and Leu anchor residue at the C-terminus. {ECO:0000269|PubMed:7743181}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for HLA-B-HLA-B


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for HLA-B-HLA-B


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for HLA-B-HLA-B


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneHLA-BP01889DB11294Coccidioides immitis spheruleBiotechApproved
HgeneHLA-BP01889DB11294Coccidioides immitis spheruleBiotechApproved
HgeneHLA-BP01889DB01048AbacavirSmall moleculeApproved|Investigational
HgeneHLA-BP01889DB01048AbacavirSmall moleculeApproved|Investigational
TgeneHLA-BP01889DB11294Coccidioides immitis spheruleBiotechApproved
TgeneHLA-BP01889DB11294Coccidioides immitis spheruleBiotechApproved
TgeneHLA-BP01889DB01048AbacavirSmall moleculeApproved|Investigational
TgeneHLA-BP01889DB01048AbacavirSmall moleculeApproved|Investigational

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Related Diseases for HLA-B-HLA-B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHLA-BC0014518Toxic Epidermal Necrolysis9CTD_human
HgeneHLA-BC0038325Stevens-Johnson Syndrome9CTD_human;ORPHANET
HgeneHLA-BC1274933Drug-Induced Stevens Johnson Syndrome9CTD_human
HgeneHLA-BC3658301Mycoplasma-Induced Stevens-Johnson Syndrome9CTD_human
HgeneHLA-BC3658302Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum9CTD_human
HgeneHLA-BC0013221Drug toxicity6CTD_human
HgeneHLA-BC0041755Adverse reaction to drug6CTD_human
HgeneHLA-BC0013182Drug Allergy4CTD_human
HgeneHLA-BC0033687Proteinuria4CTD_human
HgeneHLA-BC0038013Ankylosing spondylitis3CTD_human
HgeneHLA-BC0004943Behcet Syndrome2CTD_human;ORPHANET
HgeneHLA-BC0011603Dermatitis2CTD_human
HgeneHLA-BC0011609Drug Eruptions2CTD_human
HgeneHLA-BC0026896Myasthenia Gravis2CTD_human
HgeneHLA-BC0036341Schizophrenia2PSYGENET
HgeneHLA-BC0039263Takayasu Arteritis2ORPHANET
HgeneHLA-BC0406537Morbilliform Drug Reaction2CTD_human
HgeneHLA-BC0751339Myasthenia Gravis, Generalized2CTD_human
HgeneHLA-BC0751340Myasthenia Gravis, Ocular2CTD_human
HgeneHLA-BC0011633Dermatomyositis1CTD_human
HgeneHLA-BC0015230Exanthema1CTD_human
HgeneHLA-BC0017638Glioma1CTD_human
HgeneHLA-BC0019193Hepatitis, Toxic1CTD_human
HgeneHLA-BC0019693HIV Infections1CTD_human
HgeneHLA-BC0020517Hypersensitivity1CTD_human
HgeneHLA-BC0026654Moyamoya Disease1GENOMICS_ENGLAND
HgeneHLA-BC0027697Nephritis1CTD_human
HgeneHLA-BC0033975Psychotic Disorders1PSYGENET
HgeneHLA-BC0039103Synovitis1CTD_human
HgeneHLA-BC0221056Adult type dermatomyositis1CTD_human
HgeneHLA-BC0259783mixed gliomas1CTD_human
HgeneHLA-BC0263666Dermatomyositis, Childhood Type1CTD_human
HgeneHLA-BC0410574Synovial Hypertrophy1CTD_human
HgeneHLA-BC0555198Malignant Glioma1CTD_human
HgeneHLA-BC0860207Drug-Induced Liver Disease1CTD_human
HgeneHLA-BC1262760Hepatitis, Drug-Induced1CTD_human
HgeneHLA-BC1527304Allergic Reaction1CTD_human
HgeneHLA-BC3658290Drug-Induced Acute Liver Injury1CTD_human
HgeneHLA-BC4277682Chemical and Drug Induced Liver Injury1CTD_human
HgeneHLA-BC4279912Chemically-Induced Liver Toxicity1CTD_human
HgeneHLA-BC4505456HIV Coinfection1CTD_human
TgeneHLA-BC0014518Toxic Epidermal Necrolysis9CTD_human
TgeneHLA-BC0038325Stevens-Johnson Syndrome9CTD_human;ORPHANET
TgeneHLA-BC1274933Drug-Induced Stevens Johnson Syndrome9CTD_human
TgeneHLA-BC3658301Mycoplasma-Induced Stevens-Johnson Syndrome9CTD_human
TgeneHLA-BC3658302Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum9CTD_human
TgeneHLA-BC0013221Drug toxicity6CTD_human
TgeneHLA-BC0041755Adverse reaction to drug6CTD_human
TgeneHLA-BC0013182Drug Allergy4CTD_human
TgeneHLA-BC0033687Proteinuria4CTD_human
TgeneHLA-BC0038013Ankylosing spondylitis3CTD_human
TgeneHLA-BC0004943Behcet Syndrome2CTD_human;ORPHANET
TgeneHLA-BC0011603Dermatitis2CTD_human
TgeneHLA-BC0011609Drug Eruptions2CTD_human
TgeneHLA-BC0026896Myasthenia Gravis2CTD_human
TgeneHLA-BC0036341Schizophrenia2PSYGENET
TgeneHLA-BC0039263Takayasu Arteritis2ORPHANET
TgeneHLA-BC0406537Morbilliform Drug Reaction2CTD_human
TgeneHLA-BC0751339Myasthenia Gravis, Generalized2CTD_human
TgeneHLA-BC0751340Myasthenia Gravis, Ocular2CTD_human
TgeneHLA-BC0011633Dermatomyositis1CTD_human
TgeneHLA-BC0015230Exanthema1CTD_human
TgeneHLA-BC0017638Glioma1CTD_human
TgeneHLA-BC0019193Hepatitis, Toxic1CTD_human
TgeneHLA-BC0019693HIV Infections1CTD_human
TgeneHLA-BC0020517Hypersensitivity1CTD_human
TgeneHLA-BC0026654Moyamoya Disease1GENOMICS_ENGLAND
TgeneHLA-BC0027697Nephritis1CTD_human
TgeneHLA-BC0033975Psychotic Disorders1PSYGENET
TgeneHLA-BC0039103Synovitis1CTD_human
TgeneHLA-BC0221056Adult type dermatomyositis1CTD_human
TgeneHLA-BC0259783mixed gliomas1CTD_human
TgeneHLA-BC0263666Dermatomyositis, Childhood Type1CTD_human
TgeneHLA-BC0410574Synovial Hypertrophy1CTD_human
TgeneHLA-BC0555198Malignant Glioma1CTD_human
TgeneHLA-BC0860207Drug-Induced Liver Disease1CTD_human
TgeneHLA-BC1262760Hepatitis, Drug-Induced1CTD_human
TgeneHLA-BC1527304Allergic Reaction1CTD_human
TgeneHLA-BC3658290Drug-Induced Acute Liver Injury1CTD_human
TgeneHLA-BC4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneHLA-BC4279912Chemically-Induced Liver Toxicity1CTD_human
TgeneHLA-BC4505456HIV Coinfection1CTD_human