GRIN2A
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GRIN2A
Summary
GRIN2A is a gene[1]. GRIN2A ranks in the top 2% of gene entities by monthly Wikipedia readership (47 views/month).[2]
Key Facts
- GRIN2A's instance of is recorded as gene[3].
- GRIN2A is a type of protein-coding gene[4].
- GRIN2A's HomoloGene ID is recorded as 645[5].
- GRIN2A's genomic start is recorded as 9753404[6].
- GRIN2A's genomic start is recorded as 9852376[7].
- GRIN2A's genomic end is recorded as 10276611[8].
- GRIN2A's genomic end is recorded as 10182928[9].
- GRIN2A's ortholog is recorded as Grin2a[10].
- GRIN2A's ortholog is recorded as Grin2a[11].
- GRIN2A's ortholog is recorded as grin2aa[12].
- GRIN2A's encodes is recorded as Glutamate ionotropic receptor NMDA type subunit 2A[13].
- GRIN2A's found in taxon is recorded as Homo sapiens[14].
- GRIN2A's chromosome is recorded as human chromosome 16[15].
- GRIN2A's genetic association is recorded as hepatitis B[16].
- GRIN2A's genetic association is recorded as Landau–Kleffner syndrome[17].
- GRIN2A's genetic association is recorded as rolandic epilepsy-speech dyspraxia syndrome[18].
- GRIN2A's genetic association is recorded as benign epilepsy with centrotemporal spikes[19].
- GRIN2A's strand orientation is recorded as reverse strand[20].
- GRIN2A's exact match is recorded as http://identifiers.org/ncbigene/2903[21].
- GRIN2A's cytogenetic location is recorded as 16p13.2[22].
- GRIN2A's expressed in is recorded as Brodmann area 23[23].
- GRIN2A's expressed in is recorded as endothelial cell[24].
- GRIN2A's expressed in is recorded as middle temporal gyrus[25].
- GRIN2A's expressed in is recorded as postcentral gyrus[26].
- GRIN2A's expressed in is recorded as lateral nuclear group of thalamus[27].
Why It Matters
GRIN2A ranks in the top 2% of gene entities by monthly Wikipedia readership (47 views/month).[2] GRIN2A has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] GRIN2A is known by 7 alternative names across languages and contexts.[29]