GRIN2B
protein-coding gene in the species Homo sapiens
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GRIN2B
Summary
GRIN2B is a gene[1]. GRIN2B ranks in the top 1% of gene entities by monthly Wikipedia readership (8 views/month).[2]
Key Facts
- GRIN2B's instance of is recorded as gene[3].
- GRIN2B is a type of protein-coding gene[4].
- GRIN2B's HomoloGene ID is recorded as 646[5].
- GRIN2B's genomic start is recorded as 13437942[6].
- GRIN2B's genomic start is recorded as 13693165[7].
- GRIN2B's genomic end is recorded as 14133053[8].
- GRIN2B's genomic end is recorded as 13982002[9].
- GRIN2B's ortholog is recorded as Grin2b[10].
- GRIN2B's ortholog is recorded as Grin2b[11].
- GRIN2B's ortholog is recorded as grin2bb[12].
- GRIN2B's ortholog is recorded as grin2b[13].
- GRIN2B's encodes is recorded as Glutamate ionotropic receptor NMDA type subunit 2B[14].
- GRIN2B's found in taxon is recorded as Homo sapiens[15].
- GRIN2B's chromosome is recorded as human chromosome 12[16].
- GRIN2B's genetic association is recorded as smallpox[17].
- GRIN2B's genetic association is recorded as autosomal dominant non-syndromic intellectual disability 6[18].
- GRIN2B's strand orientation is recorded as reverse strand[19].
- GRIN2B's exact match is recorded as http://identifiers.org/ncbigene/2904[20].
- GRIN2B's cytogenetic location is recorded as 12p13.1[21].
- GRIN2B's expressed in is recorded as buccal mucosa cell[22].
- GRIN2B's expressed in is recorded as Brodmann area 23[23].
- GRIN2B's expressed in is recorded as sural nerve[24].
- GRIN2B's expressed in is recorded as middle temporal gyrus[25].
- GRIN2B's expressed in is recorded as primary visual cortex[26].
- GRIN2B's expressed in is recorded as corpus callosum[27].
Why It Matters
GRIN2B ranks in the top 1% of gene entities by monthly Wikipedia readership (8 views/month).[2] GRIN2B is known by 12 alternative names across languages and contexts.[28]