| 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.