Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
284656
Gene name Gene Name - the full gene name approved by the HGNC.
EPH receptor A10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EPHA10
Synonyms (NCBI Gene) Gene synonyms aliases
DFNA88
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DFNA88
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p34.3
Summary Summary of gene provided in NCBI Entrez Gene.
Ephrin receptors, the largest subfamily of receptor tyrosine kinases (RTKs), and their ephrin ligands are important mediators of cell-cell communication regulating cell attachment, shape, and mobility in neuronal and epithelial cells (Aasheim et al., 2005
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT966226 hsa-miR-1207-5p CLIP-seq
MIRT966227 hsa-miR-1224-5p CLIP-seq
MIRT966228 hsa-miR-124 CLIP-seq
MIRT966229 hsa-miR-1270 CLIP-seq
MIRT966230 hsa-miR-1275 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004714 Function Transmembrane receptor protein tyrosine kinase activity IBA 21873635
GO:0005005 Function Transmembrane-ephrin receptor activity IBA 21873635
GO:0005515 Function Protein binding IPI 15777695
GO:0005524 Function ATP binding IEA
GO:0005576 Component Extracellular region IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611123 19987 ENSG00000183317
Protein
UniProt ID Q5JZY3
Protein name Ephrin type-A receptor 10 (EC 2.7.10.1)
Protein function Receptor for members of the ephrin-A family. Binds to EFNA3, EFNA4 and EFNA5.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01404 Ephrin_lbd 36 211 Ephrin receptor ligand binding domain Domain
PF00041 fn3 339 436 Fibronectin type III domain Domain
PF00041 fn3 458 537 Fibronectin type III domain Domain
PF14575 EphA2_TM 567 642 Ephrin type-A receptor 2 transmembrane domain Domain
PF07714 PK_Tyr_Ser-Thr 645 900 Protein tyrosine and serine/threonine kinase Domain
PF00536 SAM_1 932 995 SAM domain (Sterile alpha motif) Domain
Tissue specificity TISSUE SPECIFICITY: Mainly expressed in testis. {ECO:0000269|PubMed:15777695}.
Sequence
METCAGPHPLRLFLCRMQLCLALLLGPWRPGTAEEVILLDSKASQAELGWTALPSNGWEE
ISGVDEHDRPIRTYQVCNVLEPNQDNWLQTGWISRGRGQRIFVELQFTLRDCSSIPGAAG
TCKETFNVYYLETEADLGRGRPRLGGSRPRKIDTIAADESFTQGDLGERKMKLNTEVREI
GPLSRRGFHLAFQDVGACVALVSVRVYYKQC
RATVRGLATFPATAAESAFSTLVEVAGTC
VAHSEGEPGSPPRMHCGADGEWLVPVGRCSCSAGFQERGDFCEACPPGFYKVSPRRPLCS
PCPEHSRALENASTFCVCQDSYARSPTDPPSASCTRPPSAPRDLQYSLSRSPLVLRLRWL
PPADSGGRSDVTYSLLCLRCGREGPAGACEPCGPRVAFLPRQAGLRERAATLLHLRPGAR
YTVRVAALNGVSGPAA
AAGTTYAQVTVSTGPGAPWEEDEIRRDRVEPQSVSLSWREPIPA
GAPGANDTEYEIRYYEKGQSEQTYSMVKTGAPTVTVTNLKPATRYVFQIRAASPGPS
WEA
QSFNPSIEVQTLGEAASGSRDQSPAIVVTVVTISALLVLGSVMSVLAIWRRPCSYGKGGG
DAHDEEELYFHFKVPTRRTFLDPQSCGDLLQAVHLFAKELDA
KSVTLERSLGGGRFGELC
CGCLQLPGRQELLVAVHMLRDSASDSQRLGFLAEALTLGQFDHSHIVRLEGVVTRGSTLM
IVTEYMSHGALDGFLRRHEGQLVAGQLMGLLPGLASAMKYLSEMGYVHRGLAARHVLVSS
DLVCKISGFGRGPRDRSEAVYTTMSGRSPALWAAPETLQFGHFSSASDVWSFGIIMWEVM
AFGERPYWDMSGQDVIKAVEDGFRLPPPRNCPNLLHRLMLDCWQKDPGERPRFSQIHSIL

SKMVQDPEPPKCALTTCPRPPTPLADRAFSTFPSFGSVGAWLEALDLCRYKDSFAAAGYG
SLEAVAEMTAQDLVSLGISLAEHREALLSGISALQ
ARVLQLQGQGVQV
Sequence length 1008
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    EPH-Ephrin signaling
EPHA-mediated growth cone collapse
EPH-ephrin mediated repulsion of cells
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Gastric cancer Gastric Adenocarcinoma rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802
View all (244 more)
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Deafness hearing loss, autosomal dominant 88 GenCC
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Myocardial Infarction Myocardial Infarction GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 35770949
Breast Neoplasms Associate 24403271, 27566654, 33977106, 33990369
Carcinoma Non Small Cell Lung Associate 39179608
Colitis Ulcerative Associate 32322884
Hereditary Breast and Ovarian Cancer Syndrome Associate 27566654
Lymphatic Metastasis Associate 24403271
Neoplasm Invasiveness Associate 33990369
Neoplasm Metastasis Associate 24403271
Neoplasms Associate 24403271
Prostatic Neoplasms Associate 38554337