Homo sapiens Gene: GFRA4
Summary
InnateDB Gene IDBG-47226.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GFRA4
Gene Name GDNF family receptor alpha 4
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000125861
Encoded Proteins
GDNF family receptor alpha 4
GDNF family receptor alpha 4
GDNF family receptor alpha 4
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol(GPI)-linked cell surface receptor for persephin, and mediates activation of the RET tyrosine kinase receptor. This gene is a candidate gene for RET-associated diseases. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:3659292-3663399
Strand Reverse strand
Band p13
Transcripts
ENST00000319242 ENSP00000313423
ENST00000290417 ENSP00000290417
ENST00000477160 ENSP00000435801
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0016167 glial cell-derived neurotrophic factor receptor activity
Biological Process
GO:0030279 negative regulation of ossification
GO:0035860 glial cell-derived neurotrophic factor receptor signaling pathway
Cellular Component
GO:0005615 extracellular space
GO:0005886 plasma membrane
GO:0031225 anchored component of membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
NCAM1 interactions pathway
NCAM signaling for neurite out-growth pathway
Developmental Biology pathway
Axon guidance pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt Q9GZZ7
TrEMBL
UniProt Splice Variant
Entrez Gene 64096
UniGene
RefSeq NM_022139 NM_145762 XM_005260793
HUGO HGNC:13821
OMIM
CCDS CCDS13055 CCDS13056
HPRD
IMGT
EMBL AF253318 AJ291673 AJ291674 AJ291675 AL356755
GenPept AAG25925 CAC16508 CAC19690 CAC19691 CAC19692 CAI23466
RNA Seq Atlas 64096