Gene Gene information from NCBI Gene database.
Entrez ID 2059
Gene name EGFR pathway substrate 8, signaling adaptor
Gene symbol EPS8
Synonyms (NCBI Gene)
DFNB102
Chromosome 12
Chromosome location 12p12.3
Summary 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.
6
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.
319
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
59
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600206 3420 ENSG00000151491
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
71
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autosomal recessive nonsyndromic hearing loss 102 Pathogenic; Likely pathogenic rs2135785787, rs587777691, rs1945698201, rs1945336251 RCV001843391
RCV000143841
RCV003990381
RCV001293014
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs61908095 RCV005916108
Adrenocortical carcinoma, hereditary Benign; Likely benign rs35885542 RCV005870917
Cervical cancer Likely benign rs61908095 RCV005916110
Cholangiocarcinoma Likely benign; Benign rs61908095, rs35885542 RCV005916114
RCV005870919
Associations from Text MiningDisease 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