| GPHN | 
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| Identifiers | 
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| Aliases | GPHN, GEPH, GPH, GPHRYN, HKPX1, MOCODC, gephyrin | 
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| External IDs | OMIM: 603930; MGI: 109602; HomoloGene: 10820; GeneCards: GPHN; OMA:GPHN - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 12 (mouse) | 
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 |  |  | Band | 12|12 C3 | Start | 78,273,153 bp | 
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 | End | 78,731,546 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | cerebellar cortex
 cerebellar hemisphere
 right hemisphere of cerebellum
 right lobe of liver
 prefrontal cortex
 right frontal lobe
 anterior cingulate cortex
 primary visual cortex
 caudate nucleus
 nucleus accumbens
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 | | Top expressed in |  | spermatid
 extensor digitorum longus muscle
 dentate gyrus of hippocampal formation granule cell
 saccule
 mammillary body
 lobe of cerebellum
 plantaris muscle
 cerebellar vermis
 muscle of thigh
 anterior amygdaloid area
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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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.