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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:BRAF-MACF1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BRAF-MACF1
FusionPDB ID: 10126
FusionGDB2.0 ID: 10126
HgeneTgene
Gene symbol

BRAF

MACF1

Gene ID

673

23499

Gene nameB-Raf proto-oncogene, serine/threonine kinasemicrotubule actin crosslinking factor 1
SynonymsB-RAF1|B-raf|BRAF1|NS7|RAFB1ABP620|ACF7|LIS9|MACF|OFC4
Cytomap

7q34

1p34.3

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase B-raf94 kDa B-raf proteinB-Raf proto-oncogene serine/threonine-protein kinase (p94)B-Raf serine/threonine-proteinmurine sarcoma viral (v-raf) oncogene homolog B1proto-oncogene B-Rafv-raf murine sarcoma viral oncogene microtubule-actin cross-linking factor 1620 kDa actin binding proteinactin cross-linking family protein 7macrophin 1 isoformtrabeculin-alpha
Modification date2020032920200313
UniProtAcc

P15056

Main function of 5'-partner protein: FUNCTION: Protein kinase involved in the transduction of mitogenic signals from the cell membrane to the nucleus (Probable). Phosphorylates MAP2K1, and thereby activates the MAP kinase signal transduction pathway (PubMed:21441910, PubMed:29433126). May play a role in the postsynaptic responses of hippocampal neurons (PubMed:1508179). {ECO:0000269|PubMed:1508179, ECO:0000269|PubMed:21441910, ECO:0000269|PubMed:29433126, ECO:0000305}.

Q9UPN3

Main function of 5'-partner protein: FUNCTION: [Isoform 2]: F-actin-binding protein which plays a role in cross-linking actin to other cytoskeletal proteins and also binds to microtubules (PubMed:15265687, PubMed:20937854). Plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex (PubMed:20937854). Acts as a positive regulator of Wnt receptor signaling pathway and is involved in the translocation of AXIN1 and its associated complex (composed of APC, CTNNB1 and GSK3B) from the cytoplasm to the cell membrane (By similarity). Has actin-regulated ATPase activity and is essential for controlling focal adhesions (FAs) assembly and dynamics (By similarity). Interaction with CAMSAP3 at the minus ends of non-centrosomal microtubules tethers microtubules minus-ends to actin filaments, regulating focal adhesion size and cell migration (PubMed:27693509). May play role in delivery of transport vesicles containing GPI-linked proteins from the trans-Golgi network through its interaction with GOLGA4 (PubMed:15265687). Plays a key role in wound healing and epidermal cell migration (By similarity). Required for efficient upward migration of bulge cells in response to wounding and this function is primarily rooted in its ability to coordinate microtubule dynamics and polarize hair follicle stem cells (By similarity). As a regulator of actin and microtubule arrangement and stabilization, it plays an essential role in neurite outgrowth, branching and spine formation during brain development (By similarity). {ECO:0000250|UniProtKB:Q9QXZ0, ECO:0000269|PubMed:15265687, ECO:0000269|PubMed:20937854, ECO:0000269|PubMed:27693509}.
Ensembl transtripts involved in fusion geneENST idsENST00000288602, ENST00000476350, 
ENST00000484793, ENST00000536367, 
ENST00000602421, ENST00000289893, 
ENST00000317713, ENST00000361689, 
ENST00000372915, ENST00000539005, 
ENST00000545844, ENST00000564288, 
ENST00000567887, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score28 X 21 X 11=646824 X 23 X 9=4968
# samples 3224
** MAII scorelog2(32/6468*10)=-4.3371758685863
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(24/4968*10)=-4.37155886261196
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: BRAF [Title/Abstract] AND MACF1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BRAF [Title/Abstract] AND MACF1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MACF1(39896580)-BRAF(140487384), # samples:4
BRAF(140494108)-MACF1(39898207), # samples:3
Anticipated loss of major functional domain due to fusion event.BRAF-MACF1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
BRAF-MACF1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
BRAF-MACF1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
BRAF-MACF1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
MACF1-BRAF seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MACF1-BRAF seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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
HgeneBRAF

GO:0000186

activation of MAPKK activity

29433126

HgeneBRAF

GO:0006468

protein phosphorylation

17563371

HgeneBRAF

GO:0010828

positive regulation of glucose transmembrane transport

23010278

HgeneBRAF

GO:0033138

positive regulation of peptidyl-serine phosphorylation

19667065

HgeneBRAF

GO:0043066

negative regulation of apoptotic process

19667065

HgeneBRAF

GO:0070374

positive regulation of ERK1 and ERK2 cascade

22065586

HgeneBRAF

GO:0071277

cellular response to calcium ion

18567582

HgeneBRAF

GO:0090150

establishment of protein localization to membrane

23010278

TgeneMACF1

GO:0030334

regulation of cell migration

27693509

TgeneMACF1

GO:0043001

Golgi to plasma membrane protein transport

15265687

TgeneMACF1

GO:0045773

positive regulation of axon extension

22705394

TgeneMACF1

GO:0051893

regulation of focal adhesion assembly

27693509



check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr7:39896580/chr1:140487384)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonRetention analysis results 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, are available here.

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

check buttonFusion gene breakpoints across MACF1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Amino Acid Sequences


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000288602BRAFchr7140494108-ENST00000545844MACF1chr139898207+766612016163422093
ENST00000288602BRAFchr7140494108-ENST00000567887MACF1chr139898207+791512016165312156
ENST00000288602BRAFchr7140494108-ENST00000372915MACF1chr139898207+752912016163422093
ENST00000288602BRAFchr7140494108-ENST00000361689MACF1chr139898207+753612016163422093
ENST00000288602BRAFchr7140494108-ENST00000539005MACF1chr139898207+766612016163422093
ENST00000288602BRAFchr7140494108-ENST00000317713MACF1chr139898207+766612016163422093
ENST00000288602BRAFchr7140494108-ENST00000564288MACF1chr139898207+791512016165312156
ENST00000288602BRAFchr7140494108-ENST00000289893MACF1chr139898207+755412016163602099

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
ENST00000288602ENST00000545844BRAFchr7140494108-MACF1chr139898207+0.0009140550.9990859
ENST00000288602ENST00000567887BRAFchr7140494108-MACF1chr139898207+0.0008961310.99910384
ENST00000288602ENST00000372915BRAFchr7140494108-MACF1chr139898207+0.0010052090.99899477
ENST00000288602ENST00000361689BRAFchr7140494108-MACF1chr139898207+0.0009903660.9990096
ENST00000288602ENST00000539005BRAFchr7140494108-MACF1chr139898207+0.0009204540.9990796
ENST00000288602ENST00000317713BRAFchr7140494108-MACF1chr139898207+0.0009204540.9990796
ENST00000288602ENST00000564288BRAFchr7140494108-MACF1chr139898207+0.0008961310.99910384
ENST00000288602ENST00000289893BRAFchr7140494108-MACF1chr139898207+0.000892090.9991079

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for BRAF-MACF1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BRAFchr7140494108MACF1chr1398982071201380NVHINTIEPVNIDYEQAADAELAWVA

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Potential FusionNeoAntigen Information of BRAF-MACF1 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
BRAF-MACF1_140494108_39898207.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
BRAF-MACF1chr7140494108chr1398982071201HLA-B18:01IEPVNIDY0.97810.9088614
BRAF-MACF1chr7140494108chr1398982071201HLA-B35:08TIEPVNIDY0.92020.8094514
BRAF-MACF1chr7140494108chr1398982071201HLA-B15:02TIEPVNIDY0.86170.9166514
BRAF-MACF1chr7140494108chr1398982071201HLA-B15:31TIEPVNIDY0.86920.8358514
BRAF-MACF1chr7140494108chr1398982071201HLA-B18:08IEPVNIDY0.98150.8591614
BRAF-MACF1chr7140494108chr1398982071201HLA-B18:06IEPVNIDY0.98130.8999614
BRAF-MACF1chr7140494108chr1398982071201HLA-B18:05IEPVNIDY0.97810.9088614
BRAF-MACF1chr7140494108chr1398982071201HLA-B18:11IEPVNIDY0.92580.7995614
BRAF-MACF1chr7140494108chr1398982071201HLA-B35:20TIEPVNIDY0.86820.8832514
BRAF-MACF1chr7140494108chr1398982071201HLA-A25:01NTIEPVNIDY0.96650.7362414

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Potential FusionNeoAntigen Information of BRAF-MACF1 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
BRAF-MACF1_140494108_39898207.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
BRAF-MACF1chr7140494108chr1398982071201DRB1-0102PVNIDYEQAADAELA823
BRAF-MACF1chr7140494108chr1398982071201DRB1-0342IEPVNIDYEQAADAE621
BRAF-MACF1chr7140494108chr1398982071201DRB1-1002PVNIDYEQAADAELA823
BRAF-MACF1chr7140494108chr1398982071201DRB1-1002EPVNIDYEQAADAEL722
BRAF-MACF1chr7140494108chr1398982071201DRB1-1476IEPVNIDYEQAADAE621
BRAF-MACF1chr7140494108chr1398982071201DRB1-1479IEPVNIDYEQAADAE621
BRAF-MACF1chr7140494108chr1398982071201DRB1-1525IEPVNIDYEQAADAE621
BRAF-MACF1chr7140494108chr1398982071201DRB3-0301NVHINTIEPVNIDYE015
BRAF-MACF1chr7140494108chr1398982071201DRB4-0101INTIEPVNIDYEQAA318
BRAF-MACF1chr7140494108chr1398982071201DRB4-0101HINTIEPVNIDYEQA217
BRAF-MACF1chr7140494108chr1398982071201DRB4-0103INTIEPVNIDYEQAA318
BRAF-MACF1chr7140494108chr1398982071201DRB4-0103HINTIEPVNIDYEQA217
BRAF-MACF1chr7140494108chr1398982071201DRB4-0106INTIEPVNIDYEQAA318
BRAF-MACF1chr7140494108chr1398982071201DRB4-0106HINTIEPVNIDYEQA217
BRAF-MACF1chr7140494108chr1398982071201DRB4-0107INTIEPVNIDYEQAA318
BRAF-MACF1chr7140494108chr1398982071201DRB4-0107HINTIEPVNIDYEQA217
BRAF-MACF1chr7140494108chr1398982071201DRB4-0108INTIEPVNIDYEQAA318
BRAF-MACF1chr7140494108chr1398982071201DRB4-0108HINTIEPVNIDYEQA217

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Fusion breakpoint peptide structures of BRAF-MACF1

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
3657IEPVNIDYEQAADABRAFMACF1chr7140494108chr1398982071201

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BRAF-MACF1

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN3657IEPVNIDYEQAADA-7.9962-8.1096
HLA-B14:023BVN3657IEPVNIDYEQAADA-5.70842-6.74372
HLA-B52:013W393657IEPVNIDYEQAADA-6.83737-6.95077
HLA-B52:013W393657IEPVNIDYEQAADA-4.4836-5.5189
HLA-A11:014UQ23657IEPVNIDYEQAADA-10.0067-10.1201
HLA-A11:014UQ23657IEPVNIDYEQAADA-9.03915-10.0745
HLA-A24:025HGA3657IEPVNIDYEQAADA-6.56204-6.67544
HLA-A24:025HGA3657IEPVNIDYEQAADA-5.42271-6.45801
HLA-B44:053DX83657IEPVNIDYEQAADA-7.85648-8.89178
HLA-B44:053DX83657IEPVNIDYEQAADA-5.3978-5.5112
HLA-A02:016TDR3657IEPVNIDYEQAADA-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of BRAF-MACF1

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
BRAF-MACF1chr7140494108chr139898207414NTIEPVNIDYAACACAATAGAACCTGTCAATATTGATTAT
BRAF-MACF1chr7140494108chr139898207514TIEPVNIDYACAATAGAACCTGTCAATATTGATTAT
BRAF-MACF1chr7140494108chr139898207614IEPVNIDYATAGAACCTGTCAATATTGATTAT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
BRAF-MACF1chr7140494108chr139898207015NVHINTIEPVNIDYEAATGTGCATATAAACACAATAGAACCTGTCAATATTGATTATGAG
BRAF-MACF1chr7140494108chr139898207217HINTIEPVNIDYEQACATATAAACACAATAGAACCTGTCAATATTGATTATGAGCAAGCT
BRAF-MACF1chr7140494108chr139898207318INTIEPVNIDYEQAAATAAACACAATAGAACCTGTCAATATTGATTATGAGCAAGCTGCC
BRAF-MACF1chr7140494108chr139898207621IEPVNIDYEQAADAEATAGAACCTGTCAATATTGATTATGAGCAAGCTGCCGATGCAGAA
BRAF-MACF1chr7140494108chr139898207722EPVNIDYEQAADAELGAACCTGTCAATATTGATTATGAGCAAGCTGCCGATGCAGAACTA
BRAF-MACF1chr7140494108chr139898207823PVNIDYEQAADAELACCTGTCAATATTGATTATGAGCAAGCTGCCGATGCAGAACTAGCT

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Information of the samples that have these potential fusion neoantigens of BRAF-MACF1

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
THCABRAF-MACF1chr7140494108ENST00000288602chr139898207ENST00000289893TCGA-DE-A0Y2-01A

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Potential target of CAR-T therapy development for BRAF-MACF1

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to BRAF-MACF1

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to BRAF-MACF1

check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBRAFC0025202melanoma24CGI;CTD_human;UNIPROT
HgeneBRAFC1275081Cardio-facio-cutaneous syndrome14CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneBRAFC0009402Colorectal Carcinoma8CTD_human;UNIPROT
HgeneBRAFC0028326Noonan Syndrome8CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneBRAFC0238463Papillary thyroid carcinoma8CTD_human;ORPHANET
HgeneBRAFC0040136Thyroid Neoplasm6CGI;CTD_human
HgeneBRAFC0151468Thyroid Gland Follicular Adenoma6CTD_human
HgeneBRAFC0175704LEOPARD Syndrome6CLINGEN;GENOMICS_ENGLAND
HgeneBRAFC0549473Thyroid carcinoma6CGI;CTD_human
HgeneBRAFC3150970NOONAN SYNDROME 75CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneBRAFC0009404Colorectal Neoplasms4CTD_human
HgeneBRAFC3150971LEOPARD SYNDROME 34CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneBRAFC1519086Pilomyxoid astrocytoma3ORPHANET
HgeneBRAFC0004565Melanoma, B162CTD_human
HgeneBRAFC0009075Melanoma, Cloudman S912CTD_human
HgeneBRAFC0018598Melanoma, Harding-Passey2CTD_human
HgeneBRAFC0023443Hairy Cell Leukemia2CGI;ORPHANET
HgeneBRAFC0025205Melanoma, Experimental2CTD_human
HgeneBRAFC0033578Prostatic Neoplasms2CTD_human
HgeneBRAFC0152013Adenocarcinoma of lung (disorder)2CGI;CTD_human
HgeneBRAFC0376358Malignant neoplasm of prostate2CTD_human
HgeneBRAFC0587248Costello syndrome (disorder)2CLINGEN;CTD_human
HgeneBRAFC3501843Nonmedullary Thyroid Carcinoma2CTD_human
HgeneBRAFC3501844Familial Nonmedullary Thyroid Cancer2CTD_human
HgeneBRAFC0002448Ameloblastoma1CTD_human
HgeneBRAFC0004114Astrocytoma1CTD_human
HgeneBRAFC0010276Craniopharyngioma1CTD_human;ORPHANET
HgeneBRAFC0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
HgeneBRAFC0017638Glioma1CGI;CTD_human
HgeneBRAFC0019621Histiocytosis, Langerhans-Cell1CGI;ORPHANET
HgeneBRAFC0022665Kidney Neoplasm1CTD_human
HgeneBRAFC0023903Liver neoplasms1CTD_human
HgeneBRAFC0024232Lymphatic Metastasis1CTD_human
HgeneBRAFC0024694Mandibular Neoplasms1CTD_human
HgeneBRAFC0027659Neoplasms, Experimental1CTD_human
HgeneBRAFC0027962Melanocytic nevus1GENOMICS_ENGLAND
HgeneBRAFC0036920Sezary Syndrome1CTD_human
HgeneBRAFC0041409Turner Syndrome, Male1CTD_human
HgeneBRAFC0079773Lymphoma, T-Cell, Cutaneous1CTD_human
HgeneBRAFC0205768Subependymal Giant Cell Astrocytoma1CTD_human
HgeneBRAFC0206686Adrenocortical carcinoma1CTD_human
HgeneBRAFC0206754Neuroendocrine Tumors1CTD_human
HgeneBRAFC0259783mixed gliomas1CTD_human
HgeneBRAFC0278875Adult Craniopharyngioma1CTD_human
HgeneBRAFC0280783Juvenile Pilocytic Astrocytoma1CTD_human
HgeneBRAFC0280785Diffuse Astrocytoma1CTD_human
HgeneBRAFC0334579Anaplastic astrocytoma1CGI;CTD_human
HgeneBRAFC0334580Protoplasmic astrocytoma1CTD_human
HgeneBRAFC0334581Gemistocytic astrocytoma1CTD_human
HgeneBRAFC0334582Fibrillary Astrocytoma1CTD_human
HgeneBRAFC0334583Pilocytic Astrocytoma1CGI;CTD_human
HgeneBRAFC0338070Childhood Cerebral Astrocytoma1CTD_human
HgeneBRAFC0345904Malignant neoplasm of liver1CTD_human
HgeneBRAFC0376407Granulomatous Slack Skin1CTD_human
HgeneBRAFC0406803Syringocystadenoma Papilliferum1GENOMICS_ENGLAND
HgeneBRAFC0431128Papillary craniopharyngioma1CTD_human
HgeneBRAFC0431129Adamantinous Craniopharyngioma1CTD_human
HgeneBRAFC0547065Mixed oligoastrocytoma1CTD_human
HgeneBRAFC0555198Malignant Glioma1CTD_human
HgeneBRAFC0596263Carcinogenesis1CTD_human
HgeneBRAFC0684249Carcinoma of lung1CGI;UNIPROT
HgeneBRAFC0740457Malignant neoplasm of kidney1CTD_human
HgeneBRAFC0750935Cerebral Astrocytoma1CTD_human
HgeneBRAFC0750936Intracranial Astrocytoma1CTD_human
HgeneBRAFC0751061Craniopharyngioma, Child1CTD_human
HgeneBRAFC0920269Microsatellite Instability1CTD_human
HgeneBRAFC1527404Female Pseudo-Turner Syndrome1CTD_human
HgeneBRAFC1704230Grade I Astrocytoma1CTD_human
HgeneBRAFC1721098Replication Error Phenotype1CTD_human
HgeneBRAFC2239176Liver carcinoma1CTD_human
HgeneBRAFC4551484Leopard Syndrome 11GENOMICS_ENGLAND
HgeneBRAFC4551602Noonan Syndrome 11CTD_human
HgeneBRAFC4721532Lymphoma, Non-Hodgkin, Familial1UNIPROT
HgeneBRAFC4733333familial non-medullary thyroid cancer1GENOMICS_ENGLAND