Gephyrin

GPHN
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGPHN, GEPH, GPH, GPHRYN, HKPX1, MOCODC, gephyrin
External IDsOMIM: 603930; MGI: 109602; HomoloGene: 10820; GeneCards: GPHN; OMA:GPHN - orthologs
Orthologs
SpeciesHumanMouse
Entrez

10243

268566

Ensembl

ENSG00000171723

ENSMUSG00000047454

UniProt

Q9NQX3

Q8BUV3

RefSeq (mRNA)

NM_145965
NM_172952

RefSeq (protein)

NP_666077
NP_766540

Location (UCSC)Chr 14: 66.51 – 67.18 MbChr 12: 78.27 – 78.73 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Gephyrin is a protein that in humans is encoded by the GPHN gene.

This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperekplexia and also lead to molybdenum cofactor deficiency.