FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact
Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:SMARCA4-ICAM1 (FusionGDB2 ID:83308)

Fusion Gene Summary for SMARCA4-ICAM1

check button Fusion gene summary
Fusion gene informationFusion gene name: SMARCA4-ICAM1
Fusion gene ID: 83308
HgeneTgene
Gene symbol

SMARCA4

ICAM1

Gene ID

6597

3383

Gene nameSWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4intercellular adhesion molecule 1
SynonymsBAF190|BAF190A|BRG1|CSS4|MRD16|RTPS2|SNF2|SNF2-beta|SNF2L4|SNF2LB|SWI2|hSNF2bBB2|CD54|P3.58
Cytomap

19p13.2

19p13.2

Type of geneprotein-codingprotein-coding
Descriptiontranscription activator BRG1ATP-dependent helicase SMARCA4BRG1-associated factor 190ABRM/SWI2-related gene 1SNF2-like 4brahma protein-like 1global transcription activator homologous sequencehomeotic gene regulatormitotic growth and transcription aintercellular adhesion molecule 1ICAM-1cell surface glycoprotein P3.58epididymis secretory sperm binding proteinintercellular adhesion molecule 1 (CD54), human rhinovirus receptormajor group rhinovirus receptor
Modification date2020031520200329
UniProtAcc.

P05362

Ensembl transtripts involved in fusion geneENST00000358026, ENST00000344626, 
ENST00000429416, ENST00000541122, 
ENST00000589677, ENST00000444061, 
ENST00000590574, ENST00000413806, 
ENST00000450717, ENST00000538456, 
ENST00000264832, ENST00000423829, 
ENST00000585443, 
Fusion gene scores* DoF score29 X 29 X 17=142972 X 3 X 2=12
# samples 553
** MAII scorelog2(55/14297*10)=-4.70013702309346
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SMARCA4 [Title/Abstract] AND ICAM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSMARCA4(11071850)-ICAM1(10385441), # samples:3
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
HgeneSMARCA4

GO:0006337

nucleosome disassembly

8895581

HgeneSMARCA4

GO:0006338

chromatin remodeling

10943845|11726552

HgeneSMARCA4

GO:0045892

negative regulation of transcription, DNA-templated

12065415

HgeneSMARCA4

GO:0045944

positive regulation of transcription by RNA polymerase II

15774904|17938176

HgeneSMARCA4

GO:0051091

positive regulation of DNA-binding transcription factor activity

11950834|17938176

HgeneSMARCA4

GO:1902661

positive regulation of glucose mediated signaling pathway

22368283

TgeneICAM1

GO:0007155

cell adhesion

16809613

TgeneICAM1

GO:0044406

adhesion of symbiont to host

2538243

TgeneICAM1

GO:0046813

receptor-mediated virion attachment to host cell

2538243

TgeneICAM1

GO:1902042

negative regulation of extrinsic apoptotic signaling pathway via death domain receptors

10903502

TgeneICAM1

GO:1904646

cellular response to amyloid-beta

11078691

TgeneICAM1

GO:2000352

negative regulation of endothelial cell apoptotic process

10903502


check buttonFusion gene breakpoints across SMARCA4 (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 ICAM1 (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
ChimerDB4BRCATCGA-AR-A256-01ASMARCA4chr19

11071850

+ICAM1chr19

10385441

+
ChimerDB4BRCATCGA-AR-A256SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
ChimerDB4BRCATCGA-AR-A256-01ASMARCA4chr19

11071850

+ICAM1chr19

10385441

+
ChimerDB4BRCATCGA-AR-A256-01ASMARCA4chr19

11071850

-ICAM1chr19

10385441

+


Top

Fusion Gene ORF analysis for SMARCA4-ICAM1

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
5UTR-3CDSENST00000358026ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000358026ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000358026ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-3CDSENST00000344626ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000344626ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000344626ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-3CDSENST00000429416ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000429416ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000429416ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-3CDSENST00000541122ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000541122ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000541122ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-3CDSENST00000589677ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000589677ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000589677ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-3CDSENST00000444061ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000444061ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-intronENST00000444061ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-3CDSENST00000590574ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000590574ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000590574ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-3CDSENST00000413806ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000413806ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000413806ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-3CDSENST00000450717ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000450717ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000450717ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-3CDSENST00000538456ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000538456ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
intron-intronENST00000538456ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385441

+
5UTR-3CDSENST00000358026ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000358026ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000358026ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-3CDSENST00000344626ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000344626ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000344626ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-3CDSENST00000429416ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000429416ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000429416ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-3CDSENST00000541122ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000541122ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000541122ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-3CDSENST00000589677ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000589677ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000589677ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-3CDSENST00000444061ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000444061ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
5UTR-intronENST00000444061ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-3CDSENST00000590574ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000590574ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000590574ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-3CDSENST00000413806ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000413806ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000413806ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-3CDSENST00000450717ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000450717ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000450717ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-3CDSENST00000538456ENST00000264832SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000538456ENST00000423829SMARCA4chr19

11071850

+ICAM1chr19

10385440

+
intron-intronENST00000538456ENST00000585443SMARCA4chr19

11071850

+ICAM1chr19

10385440

+

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

Top

Fusion Genomic Features for SMARCA4-ICAM1


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)
SMARCA4chr1911071850+ICAM1chr1910385440+2.12E-131
SMARCA4chr1911071850+ICAM1chr1910385440+2.12E-131
SMARCA4chr1911071850+ICAM1chr1910385440+2.12E-131
SMARCA4chr1911071850+ICAM1chr1910385440+2.12E-131

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.

Top

Fusion Protein Features for SMARCA4-ICAM1


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
.ICAM1

P05362

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: ICAM proteins are ligands for the leukocyte adhesion protein LFA-1 (integrin alpha-L/beta-2). During leukocyte trans-endothelial migration, ICAM1 engagement promotes the assembly of endothelial apical cups through ARHGEF26/SGEF and RHOG activation. {ECO:0000269|PubMed:11173916, ECO:0000269|PubMed:17875742}.; FUNCTION: (Microbial infection) Acts as a receptor for major receptor group rhinovirus A-B capsid proteins. {ECO:0000269|PubMed:1968231, ECO:0000269|PubMed:2538243}.; FUNCTION: (Microbial infection) Acts as a receptor for Coxsackievirus A21 capsid proteins. {ECO:0000269|PubMed:11160747, ECO:0000269|PubMed:16004874, ECO:0000269|PubMed:9539703}.; FUNCTION: (Microbial infection) Upon Kaposi's sarcoma-associated herpesvirus/HHV-8 infection, is degraded by viral E3 ubiquitin ligase MIR2, presumably to prevent lysis of infected cells by cytotoxic T-lymphocytes and NK cell. {ECO:0000269|PubMed:11413168}.

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


Top

Fusion Gene Sequence for SMARCA4-ICAM1


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 SMARCA4-ICAM1


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


Top

Related Drugs for SMARCA4-ICAM1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneICAM1P05362DB00108NatalizumabBiotechApproved|Investigational
TgeneICAM1P05362DB08818Hyaluronic acidSmall moleculeApproved|Vet_approved

Top

Related Diseases for SMARCA4-ICAM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSMARCA4C2750074Rhabdoid Tumor Predisposition Syndrome 27CLINGEN;CTD_human;GENOMICS_ENGLAND
HgeneSMARCA4C0262584Carcinoma, Small Cell4CTD_human
HgeneSMARCA4C0919267ovarian neoplasm4CGI;CTD_human
HgeneSMARCA4C1140680Malignant neoplasm of ovary4CGI;CTD_human
HgeneSMARCA4C0009405Hereditary Nonpolyposis Colorectal Neoplasms2CLINGEN
HgeneSMARCA4C1112155Hereditary non-polyposis colorectal cancer syndrome2CLINGEN
HgeneSMARCA4C1333990Hereditary Nonpolyposis Colorectal Cancer2CLINGEN
HgeneSMARCA4C1333991Hereditary Non-Polyposis Colon Cancer Type 22CLINGEN
HgeneSMARCA4C2936783Colorectal cancer, hereditary nonpolyposis, type 12CLINGEN
HgeneSMARCA4C2985524Rhabdoid tumor predisposition syndrome2ORPHANET
HgeneSMARCA4C0006413Burkitt Lymphoma1CTD_human
HgeneSMARCA4C0009171Cocaine Abuse1CTD_human
HgeneSMARCA4C0036920Sezary Syndrome1CTD_human
HgeneSMARCA4C0039981Thoracic Neoplasms1CTD_human
HgeneSMARCA4C0149925Small cell carcinoma of lung1CTD_human
HgeneSMARCA4C0205944Sarcoma, Epithelioid1CTD_human
HgeneSMARCA4C0205945Sarcoma, Spindle Cell1CTD_human
HgeneSMARCA4C0236736Cocaine-Related Disorders1CTD_human
HgeneSMARCA4C0265338Coffin-Siris syndrome1CTD_human;GENOMICS_ENGLAND
HgeneSMARCA4C0343640African Burkitt's lymphoma1CTD_human
HgeneSMARCA4C0600427Cocaine Dependence1CTD_human
HgeneSMARCA4C1261473Sarcoma1CTD_human
HgeneSMARCA4C1961099Precursor T-Cell Lymphoblastic Leukemia-Lymphoma1CTD_human
HgeneSMARCA4C2239246Endometrial stromal sarcoma, high grade1GENOMICS_ENGLAND
HgeneSMARCA4C3281201MENTAL RETARDATION, AUTOSOMAL DOMINANT 121GENOMICS_ENGLAND
HgeneSMARCA4C3553249COFFIN-SIRIS SYNDROME 41GENOMICS_ENGLAND;UNIPROT
HgeneSMARCA4C4721444Burkitt Leukemia1CTD_human
TgeneICAM1C0002152Alloxan Diabetes3CTD_human
TgeneICAM1C0011853Diabetes Mellitus, Experimental3CTD_human
TgeneICAM1C0038433Streptozotocin Diabetes3CTD_human
TgeneICAM1C0004096Asthma2CTD_human
TgeneICAM1C0004943Behcet Syndrome2CTD_human
TgeneICAM1C0007102Malignant tumor of colon2CTD_human
TgeneICAM1C0007222Cardiovascular Diseases2CTD_human
TgeneICAM1C0007786Brain Ischemia2CTD_human
TgeneICAM1C0009375Colonic Neoplasms2CTD_human
TgeneICAM1C0019284Diaphragmatic Hernia2CTD_human
TgeneICAM1C0020538Hypertensive disease2CTD_human
TgeneICAM1C0021368Inflammation2CTD_human
TgeneICAM1C0035126Reperfusion Injury2CTD_human
TgeneICAM1C0242488Acute Lung Injury2CTD_human
TgeneICAM1C0917798Cerebral Ischemia2CTD_human
TgeneICAM1C0004153Atherosclerosis1CTD_human
TgeneICAM1C0006267Bronchiectasis1CTD_human
TgeneICAM1C0008370Cholestasis1CTD_human
TgeneICAM1C0009324Ulcerative Colitis1CTD_human
TgeneICAM1C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
TgeneICAM1C0011884Diabetic Retinopathy1CTD_human
TgeneICAM1C0020443Hypercholesterolemia1CTD_human
TgeneICAM1C0021390Inflammatory Bowel Diseases1CTD_human
TgeneICAM1C0026640Mouth Neoplasms1CTD_human
TgeneICAM1C0026769Multiple Sclerosis1CTD_human
TgeneICAM1C0027051Myocardial Infarction1CTD_human
TgeneICAM1C0027055Myocardial Reperfusion Injury1CTD_human
TgeneICAM1C0027720Nephrosis1CTD_human
TgeneICAM1C0028754Obesity1CTD_human
TgeneICAM1C0032231Pleurisy1CTD_human
TgeneICAM1C0033578Prostatic Neoplasms1CTD_human
TgeneICAM1C0035235Respiratory Syncytial Virus Infections1CTD_human
TgeneICAM1C0035309Retinal Diseases1CTD_human
TgeneICAM1C0036341Schizophrenia1PSYGENET
TgeneICAM1C0036982Shock, Hemorrhagic1CTD_human
TgeneICAM1C0038454Cerebrovascular accident1CTD_human
TgeneICAM1C0041948Uremia1CTD_human
TgeneICAM1C0042109Urticaria1CTD_human
TgeneICAM1C0085129Bronchial Hyperreactivity1CTD_human
TgeneICAM1C0151744Myocardial Ischemia1CTD_human
TgeneICAM1C0153381Malignant neoplasm of mouth1CTD_human
TgeneICAM1C0238281Middle Cerebral Artery Syndrome1CTD_human
TgeneICAM1C0282548Leukostasis1CTD_human
TgeneICAM1C0376358Malignant neoplasm of prostate1CTD_human
TgeneICAM1C0740376Middle Cerebral Artery Thrombosis1CTD_human
TgeneICAM1C0740391Middle Cerebral Artery Occlusion1CTD_human
TgeneICAM1C0740392Infarction, Middle Cerebral Artery1CTD_human
TgeneICAM1C0751324Multiple Sclerosis, Acute Fulminating1CTD_human
TgeneICAM1C0751845Middle Cerebral Artery Embolus1CTD_human
TgeneICAM1C0751846Left Middle Cerebral Artery Infarction1CTD_human
TgeneICAM1C0751847Embolic Infarction, Middle Cerebral Artery1CTD_human
TgeneICAM1C0751848Thrombotic Infarction, Middle Cerebral Artery1CTD_human
TgeneICAM1C0751849Right Middle Cerebral Artery Infarction1CTD_human
TgeneICAM1C0751956Acute Cerebrovascular Accidents1CTD_human
TgeneICAM1C1563937Atherogenesis1CTD_human
TgeneICAM1C4721453Peripheral Nervous System Diseases1CTD_human