GRIA3
protein-coding gene in the species Homo sapiens
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GRIA3
Summary
GRIA3 is a gene[1].
Key Facts
- GRIA3's instance of is recorded as gene[2].
- GRIA3 is a type of protein-coding gene[3].
- GRIA3's HomoloGene ID is recorded as 37353[4].
- GRIA3's genomic start is recorded as 123184153[5].
- GRIA3's genomic start is recorded as 122318006[6].
- GRIA3's genomic end is recorded as 123490915[7].
- GRIA3's genomic end is recorded as 122624766[8].
- GRIA3's ortholog is recorded as Gria3[9].
- GRIA3's ortholog is recorded as Gria3[10].
- GRIA3's ortholog is recorded as gria3b[11].
- GRIA3's ortholog is recorded as GluRIA[12].
- GRIA3's ortholog is recorded as glr-1[13].
- GRIA3's ortholog is recorded as gria3a[14].
- GRIA3's ortholog is recorded as GluRIB[15].
- GRIA3's ortholog is recorded as glr-2[16].
- GRIA3's encodes is recorded as Glutamate ionotropic receptor AMPA type subunit 3[17].
- GRIA3's found in taxon is recorded as Homo sapiens[18].
- GRIA3's chromosome is recorded as human X chromosome[19].
- GRIA3's genetic association is recorded as syndromic X-linked intellectual disability 94[20].
- GRIA3's strand orientation is recorded as forward strand[21].
- GRIA3's exact match is recorded as http://identifiers.org/ncbigene/2892[22].
- GRIA3's cytogenetic location is recorded as Xq25[23].
- GRIA3's expressed in is recorded as Brodmann area 23[24].
- GRIA3's expressed in is recorded as middle temporal gyrus[25].
- GRIA3's expressed in is recorded as primary visual cortex[26].