BTBD8
protein-coding gene in the species Homo sapiens
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BTBD8
Summary
BTBD8 is a gene[1].
Key Facts
- BTBD8's instance of is recorded as gene[2].
- BTBD8 is a type of protein-coding gene[3].
- BTBD8's HomoloGene ID is recorded as 82388[4].
- BTBD8's genomic start is recorded as 92080305[5].
- BTBD8's genomic start is recorded as 92545862[6].
- BTBD8's genomic end is recorded as 92613393[7].
- BTBD8's genomic end is recorded as 92184725[8].
- BTBD8's ortholog is recorded as Btbd8[9].
- BTBD8's ortholog is recorded as Btbd8[10].
- BTBD8's ortholog is recorded as btbd8[11].
- BTBD8's encodes is recorded as BTB domain containing 8[12].
- BTBD8's found in taxon is recorded as Homo sapiens[13].
- BTBD8's chromosome is recorded as human chromosome 1[14].
- BTBD8's genetic association is recorded as obesity[15].
- BTBD8's strand orientation is recorded as forward strand[16].
- BTBD8's exact match is recorded as http://identifiers.org/ncbigene/284697[17].
- BTBD8's cytogenetic location is recorded as 1p22.1[18].
- BTBD8's expressed in is recorded as Brodmann area 23[19].
- BTBD8's expressed in is recorded as endothelial cell[20].
- BTBD8's expressed in is recorded as Brodmann area 10[21].
- BTBD8's expressed in is recorded as primary visual cortex[22].
- BTBD8's expressed in is recorded as middle temporal gyrus[23].
- BTBD8's expressed in is recorded as superior frontal gyrus[24].
- BTBD8's expressed in is recorded as orbitofrontal cortex[25].
- BTBD8's expressed in is recorded as frontal pole[26].