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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:COMT-PCBP2 (FusionGDB2 ID:18572)

Fusion Gene Summary for COMT-PCBP2

check button Fusion gene summary
Fusion gene informationFusion gene name: COMT-PCBP2
Fusion gene ID: 18572
HgeneTgene
Gene symbol

COMT

PCBP2

Gene ID

1312

5094

Gene namecatechol-O-methyltransferasepoly(rC) binding protein 2
SynonymsHEL-S-98nHNRNPE2|HNRPE2|hnRNP-E2
Cytomap

22q11.21

12q13.13

Type of geneprotein-codingprotein-coding
Descriptioncatechol O-methyltransferasecatechol-O-methyltransferase isoformepididymis secretory sperm binding protein Li 98ntesticular tissue protein Li 42poly(rC)-binding protein 2alpha-CP2epididymis secretory sperm binding proteinheterogeneous nuclear ribonucleoprotein E2heterogenous nuclear ribonucleoprotein E2hnRNP E2
Modification date2020032920200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000361682, ENST00000403184, 
ENST00000403710, ENST00000407537, 
ENST00000406520, ENST00000449653, 
ENST00000493893, 		ENST00000359282, 
ENST00000603815, ENST00000437231, 
ENST00000447282, ENST00000549863, 
ENST00000359462, ENST00000546463, 
ENST00000552296, ENST00000552819, 
ENST00000455667, ENST00000439930, 
ENST00000548933, ENST00000541275, 
Fusion gene scores* DoF score13 X 12 X 5=78027 X 26 X 9=6318
# samples 1530
** MAII scorelog2(15/780*10)=-2.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(30/6318*10)=-4.39643353125099
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COMT [Title/Abstract] AND PCBP2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOMT(19957775)-PCBP2(53849736), # 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
HgeneCOMT

GO:0042424

catecholamine catabolic process

15645182|21846718

TgenePCBP2

GO:0039694

viral RNA genome replication

12414943

TgenePCBP2

GO:0075522

IRES-dependent viral translational initiation

12414943


check buttonFusion gene breakpoints across COMT (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 PCBP2 (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/AAI360037COMTchr22

19957775

+PCBP2chr12

53849736

-


Top

Fusion Gene ORF analysis for COMT-PCBP2

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-3CDSENST00000361682ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000361682ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403184ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000403710ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000407537ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000406520ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000449653ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000359282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000603815COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000437231COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000447282COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000549863COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000359462COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000546463COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000552296COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000552819COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000455667COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000439930COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000548933COMTchr22

19957775

+PCBP2chr12

53849736

-
intron-3CDSENST00000493893ENST00000541275COMTchr22

19957775

+PCBP2chr12

53849736

-

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 COMT-PCBP2


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 COMT-PCBP2


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
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 COMT-PCBP2


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.

Top

Fusion Gene PPI Analysis for COMT-PCBP2


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 COMT-PCBP2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for COMT-PCBP2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCOMTC0005586Bipolar Disorder6CTD_human;PSYGENET
HgeneCOMTC0001723Affective Disorders, Psychotic5PSYGENET
HgeneCOMTC0011570Mental Depression5PSYGENET
HgeneCOMTC0011581Depressive disorder5PSYGENET
HgeneCOMTC0041696Unipolar Depression5PSYGENET
HgeneCOMTC0525045Mood Disorders5PSYGENET
HgeneCOMTC1269683Major Depressive Disorder5PSYGENET
HgeneCOMTC0036341Schizophrenia4CTD_human
HgeneCOMTC0005587Depression, Bipolar3CTD_human;PSYGENET
HgeneCOMTC0006142Malignant neoplasm of breast3CTD_human
HgeneCOMTC0024809Marijuana Abuse3PSYGENET
HgeneCOMTC0600427Cocaine Dependence3CTD_human;PSYGENET
HgeneCOMTC0678222Breast Carcinoma3CTD_human
HgeneCOMTC1257931Mammary Neoplasms, Human3CTD_human
HgeneCOMTC1458155Mammary Neoplasms3CTD_human
HgeneCOMTC4704874Mammary Carcinoma, Human3CTD_human
HgeneCOMTC0233477Dysphoric mood2PSYGENET
HgeneCOMTC3160814Cannabis use2PSYGENET
HgeneCOMTC0001956Alcohol Use Disorder1CTD_human
HgeneCOMTC0001973Alcoholic Intoxication, Chronic1CTD_human
HgeneCOMTC0004352Autistic Disorder1CTD_human
HgeneCOMTC0004930Behavior Disorders1CTD_human
HgeneCOMTC0004936Mental disorders1CTD_human
HgeneCOMTC0009171Cocaine Abuse1CTD_human
HgeneCOMTC0009241Cognition Disorders1CTD_human
HgeneCOMTC0012236DiGeorge Syndrome1CTD_human;ORPHANET
HgeneCOMTC0015934Fetal Growth Retardation1CTD_human
HgeneCOMTC0020429Hyperalgesia1CTD_human
HgeneCOMTC0024667Animal Mammary Neoplasms1CTD_human
HgeneCOMTC0024713Manic Disorder1CTD_human
HgeneCOMTC0025261Memory Disorders1CTD_human
HgeneCOMTC0026858Musculoskeletal Pain1CTD_human
HgeneCOMTC0030193Pain1CTD_human
HgeneCOMTC0031511Pheochromocytoma1CTD_human
HgeneCOMTC0033578Prostatic Neoplasms1CTD_human
HgeneCOMTC0039494Temporomandibular Joint Disorders1CTD_human
HgeneCOMTC0041671Attention Deficit Disorder1CTD_human
HgeneCOMTC0085762Alcohol abuse1CTD_human
HgeneCOMTC0086133Depressive Syndrome1PSYGENET
HgeneCOMTC0178417Anhedonia1PSYGENET
HgeneCOMTC0220704Shprintzen syndrome1CTD_human;ORPHANET
HgeneCOMTC0233794Memory impairment1CTD_human
HgeneCOMTC0234230Pain, Burning1CTD_human
HgeneCOMTC0234238Ache1CTD_human
HgeneCOMTC0234254Radiating pain1CTD_human
HgeneCOMTC0236733Amphetamine-Related Disorders1CTD_human
HgeneCOMTC0236736Cocaine-Related Disorders1CTD_human
HgeneCOMTC0236804Amphetamine Addiction1CTD_human
HgeneCOMTC0236807Amphetamine Abuse1CTD_human
HgeneCOMTC0338831Manic1CTD_human
HgeneCOMTC0376338Diagnosis, Psychiatric1CTD_human
HgeneCOMTC0376358Malignant neoplasm of prostate1CTD_human
HgeneCOMTC0458247Allodynia1CTD_human
HgeneCOMTC0458257Pain, Splitting1CTD_human
HgeneCOMTC0458259Pain, Crushing1CTD_human
HgeneCOMTC0525046Schizophrenia Spectrum and Other Psychotic Disorders1CTD_human
HgeneCOMTC0751211Hyperalgesia, Primary1CTD_human
HgeneCOMTC0751212Hyperalgesia, Secondary1CTD_human
HgeneCOMTC0751213Tactile Allodynia1CTD_human
HgeneCOMTC0751214Hyperalgesia, Thermal1CTD_human
HgeneCOMTC0751292Age-Related Memory Disorders1CTD_human
HgeneCOMTC0751293Memory Disorder, Semantic1CTD_human
HgeneCOMTC0751294Memory Disorder, Spatial1CTD_human
HgeneCOMTC0751295Memory Loss1CTD_human
HgeneCOMTC0751407Pain, Migratory1CTD_human
HgeneCOMTC0751408Suffering, Physical1CTD_human
HgeneCOMTC0795907CONOTRUNCAL ANOMALY FACE SYNDROME1CTD_human;ORPHANET
HgeneCOMTC1257877Pheochromocytoma, Extra-Adrenal1CTD_human
HgeneCOMTC1257925Mammary Carcinoma, Animal1CTD_human
HgeneCOMTC1263846Attention deficit hyperactivity disorder1CTD_human
HgeneCOMTC1306067Drug-induced paranoid state1PSYGENET
HgeneCOMTC1321905Minimal Brain Dysfunction1CTD_human
HgeneCOMTC2239176Liver carcinoma1CTD_human
HgeneCOMTC2750088HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO1CTD_human
HgeneCOMTC2936719Mechanical Allodynia1CTD_human
HgeneCOMTC3888239HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 11GENOMICS_ENGLAND
HgeneCOMTC4046029Mental Disorders, Severe1CTD_human