GRIN1
protein-coding gene in the species Homo sapiens
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Summary
GRIN1 is a gene[1]. GRIN1 ranks in the top 1% of gene entities by monthly Wikipedia readership (57 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 7187[4]
- Genomic start: 140032842[5], 137139154[6]
- Genomic end: 140063207[7], 137168756[8]
- Ortholog: Grin1[9], Nmdar1[10], nmr-1[11], grin1a[12], grin1b[13]
- Encodes: Glutamate ionotropic receptor NMDA type subunit 1[14]
- Found in taxon: Homo sapiens[15]
- Chromosome: human chromosome 9[16]
- Genetic association: autosomal dominant non-syndromic intellectual disability 8[17]
- Strand orientation: forward strand[18]
- Exact match: http://identifiers.org/ncbigene/2902[19]
- Cytogenetic location: 9q34.3[20]
- Expressed in: right hemisphere of cerebellum[21], right frontal lobe[22], anterior cingulate cortex[23], nucleus accumbens[24], prefrontal cortex[25], Brodmann area 9[26], putamen[27], amygdala[28], caudate nucleus[29], Brodmann area 10[30]
Why It Matters
GRIN1 has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[31] GRIN1 is known by 11 alternative names across languages and contexts.[32]