EPHB1


Summary: Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of 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. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. The protein encoded by this gene is a receptor for ephrin-B family members. [provided by RefSeq, Jul 2008].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:600600
PHARMGKB IDPA27824
Map Location3q22.2

GO terms in EPHB1


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Term Type
Evidence Type
GO Term ID
GO Des.
MF IBA GO:0004709 MAP kinase kinase kinase activity
MF EXP GO:0004713 protein tyrosine kinase activity
MF IBA GO:0004713 protein tyrosine kinase activity
MF IBA GO:0004714 transmembrane receptor protein tyrosine kinase activity
MF IBA GO:0004888 transmembrane signaling receptor activity
MF IBA GO:0005005 transmembrane-ephrin receptor activity
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Gene expression in normal tissue: EPHB1

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in EPHB1


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Database
Pathway ID
Pathway Des.
pid ephbfwdpathway EPHB forward signaling
pid ephrinbrevpathway Ephrin B reverse signaling
kegg hsa04360 Axon guidance - Homo sapiens (human)
netpath Pathway_EGFR1 EGFR1
reactome R-HSA-1266738 Developmental Biology
reactome R-HSA-1266738 Developmental Biology
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD387 CHIR-99021 2
iGMDRD420 Leucascandrolide A 2
iGMDRD1008 SR-II-138A 1
iGMDRD670 ML 210 3
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in EPHB1

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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