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Gene : EPHA8 Homo sapiens

Name  ? EPH receptor A8 Cytological Location  1p36.12
Brief Description  EPH receptor A8
Description  This gene encodes a member of the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. The protein encoded by this gene functions as a receptor for ephrin A2, A3 and A5 and plays a role in short-range contact-mediated axonal guidance during development of the mammalian nervous system. [provided by RefSeq, Jul 2008]
  • synonyms:
  • HEK3,
  • BC038796,
  • EEK,
  • Hek3,
  • EK3,
  • HGNC:3391,
  • NM_020526,
  • EphA8,
  • EEK,
  • uc001bfx.2,
  • OTTHUMG00000002892,
  • EPHA8
  • identifiers:
  • 2046,
  • ENSG00000070886,
  • EPHA8

Genome feature

Region: gene ? Length: 40107  
Location: 1:22563489-22603595 Cyto location: 1p36.12


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Genomics

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Proteins

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SNPs

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Disease

0 Diseases

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Expression

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Other

314 SN Ps

5 Cross References

17 Data Sets

58 Homologues

0 Located Features

97 Rna Seq Results