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Protein-coding gene in the species Homo sapiens

ERBB4

ERBB4
All data from the card 19
Aliases
ERBB4, ALS19, HER4, p180erbB4, erb-b2 receptor tyrosine kinase 4
External IDs
OMIM: 600543; MGI: 104771; GeneCards: ERBB4
PDB
Ortholog search: PDBe RCSB
2.7.10.1
↗
Chr.
Chromosome 2 (human)
Band
2q34
End
212,538,841 bp
Chr.
Chromosome 1 (mouse)
Band
1 C3|1 33.8 cM
End
69,147,218 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
2066
Ensembl
ENSG00000178568
UniProt
Q15303
RefSeq (mRNA)
NM_001042599NM_005235
RefSeq (protein)
NP_001036064NP_005226
Location (UCSC)
Chr 2: 211.38 – 212.54 Mb

Receptor tyrosine-protein kinase erbB-4 is an enzyme that in humans is encoded by the ERBB4 gene. Alternatively spliced variants that encode different protein isoforms have been described; however, not all variants have been fully characterized.

Function

Receptor tyrosine-protein kinase erbB-4 is a receptor tyrosine kinase that is a member of the epidermal growth factor receptor family. ERBB4 is a single-pass type I transmembrane protein with multiple furin-like cysteine rich domains, a tyrosine kinase domain, a phosphotidylinositol-3 kinase binding site and a PDZ domain binding motif. The protein binds to and is activated by neuregulins-2, -3 and -4, heparin-binding EGF-like growth factor and betacellulin. Ligand binding induces a variety of cellular responses including mitogenesis and differentiation. Multiple proteolytic events allow for the release of a cytoplasmic fragment and an extracellular fragment.

Clinical significance

Mutations in this gene have been associated with cancer. Other single-nucleotide polymorphisms and a risk haplotype have been linked to schizophrenia. Single-nucleotide polymorphisms in ERBB4 have also been found in a study of patients with familial amyotrophic lateral sclerosis type 19.

Interactions

ERBB4 has been shown to interact with:

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Text from Wikipedia, CC BY-SA 4.0 · Source article