Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2059
Gene name Gene Name - the full gene name approved by the HGNC.
EGFR pathway substrate 8, signaling adaptor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EPS8
Synonyms (NCBI Gene) Gene synonyms aliases
DFNB102
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12p12.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the EPS8 family. This protein contains one PH domain and one SH3 domain. It functions as part of the EGFR pathway, though its exact role has not been determined. Highly similar proteins in other organisms are involved in the
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs139258361 A>G Conflicting-interpretations-of-pathogenicity, not-provided, uncertain-significance Missense variant, coding sequence variant
rs142733590 G>T Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs149455769 G>A Conflicting-interpretations-of-pathogenicity Synonymous variant, coding sequence variant
rs180899529 T>C,G Pathogenic Intron variant
rs184886917 T>C,G Conflicting-interpretations-of-pathogenicity Synonymous variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT024889 hsa-miR-215-5p Microarray 19074876
MIRT026253 hsa-miR-192-5p Microarray 19074876
MIRT507381 hsa-miR-543 PAR-CLIP 22012620
MIRT507380 hsa-miR-606 PAR-CLIP 22012620
MIRT507379 hsa-miR-181a-5p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IBA
GO:0003779 Function Actin binding IEA
GO:0003779 Function Actin binding ISS
GO:0005515 Function Protein binding IPI 15289329, 16189514, 16688213, 19564905, 21098279, 21988832, 22921828, 23314863, 24076653, 24584464, 24658140, 25416956, 25814554, 31980649, 33961781, 35384245
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600206 3420 ENSG00000151491
Protein
UniProt ID Q12929
Protein name Epidermal growth factor receptor kinase substrate 8
Protein function Signaling adapter that controls various cellular protrusions by regulating actin cytoskeleton dynamics and architecture. Depending on its association with other signal transducers, can regulate different processes. Together with SOS1 and ABI1, f
PDB 2E8M , 7TZK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08416 PTB 64 194 Phosphotyrosine-binding domain Domain
PF00018 SH3_1 537 582 SH3 domain Domain
PF18016 SAM_3 716 778 SAM domain (Sterile alpha motif) Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in all tissues analyzed, including heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Expressed in all epithelial and fibroblastic lines examined and in some, but not all, hematopoietic cells.
Sequence
MNGHISNHPSSFGMYPSQMNGYGSSPTFSQTDREHGSKTSAKALYEQRKNYARDSVSSVS
DISQYRVEHLTTFVLDRKDAMITVDDGIRKLKLLDAKGKVWTQDMILQVDDRAVSLIDLE
SKNELENFPLNTIQHCQAVMHSCSYDSVLALVCKEPTQNKPDLHLFQCDEVKANLISEDI
ESAISDSKGGKQKR
RPDALRMISNADPSIPPPPRAPAPAPPGTVTQVDVRSRVAAWSAWA
ADQGDFEKPRQYHEQEETPEMMAARIDRDVQILNHILDDIEFFITKLQKAAEAFSELSKR
KKNKKGKRKGPGEGVLTLRAKPPPPDEFLDCFQKFKHGFNLLAKLKSHIQNPSAADLVHF
LFTPLNMVVQATGGPELASSVLSPLLNKDTIDFLNYTVNGDERQLWMSLGGTWMKARAEW
PKEQFIPPYVPRFRNGWEPPMLNFMGATMEQDLYQLAESVANVAEHQRKQEIKRLSTEHS
SVSEYHPADGYAFSSNIYTRGSHLDQGEAAVAFKPTSNRHIDRNYEPLKTQPKKYAKSKY
DFVARNNSELSVLKDDILEILDDRKQWWKVRNASGDSGFVPN
NILDIVRPPESGLGRADP
PYTHTIQKQRMEYGPRPADTPPAPSPPPTPAPVPVPLPPSTPAPVPVSKVPANITRQNSS
SSDSGGSIVRDSQRHKQLPVDRRKSQMEEVQDELIHRLTIGRSAAQKKFHVPRQNVPVIN
ITYDSTPEDVKTWLQSKGFNPVTVNSLGVLNGAQLFSLNKDELRTVCPEGARVYSQIT
VQ
KAALEDSSGSSELQEIMRRRQEKISAAASDSGVESFDEGSSH
Sequence length 822
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Deafness Autosomal recessive nonsyndromic hearing loss 102 rs587777691 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Hearing Loss Hearing loss, autosomal recessive 106, Hearing loss, autosomal recessive N/A N/A ClinVar
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Inhibit 22876043
Carcinogenesis Associate 22876043, 32641864
Carcinoma Pancreatic Ductal Associate 28608476, 32899691, 35848896
Carcinoma Squamous Cell Associate 30597261
Cholangiocarcinoma Associate 18839982
Colonic Neoplasms Associate 22876043
Colorectal Neoplasms Associate 22876043
Epidermodysplasia Verruciformis Associate 35848896
Lung Neoplasms Associate 24367505
Neoplasm Metastasis Associate 25936538, 27573546, 31488087