FAM171B
protein-coding gene in the species Homo sapiens
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FAM171B
Summary
FAM171B is a gene[1].
Key Facts
- FAM171B's instance of is recorded as gene[2].
- FAM171B is a type of protein-coding gene[3].
- FAM171B's HomoloGene ID is recorded as 18462[4].
- FAM171B's genomic start is recorded as 187558698[5].
- FAM171B's genomic start is recorded as 186694060[6].
- FAM171B's genomic end is recorded as 187630685[7].
- FAM171B's genomic end is recorded as 186765959[8].
- FAM171B's ortholog is recorded as Fam171b[9].
- FAM171B's ortholog is recorded as Fam171b[10].
- FAM171B's ortholog is recorded as fam171b[11].
- FAM171B's encodes is recorded as Family with sequence similarity 171 member B[12].
- FAM171B's found in taxon is recorded as Homo sapiens[13].
- FAM171B's chromosome is recorded as human chromosome 2[14].
- FAM171B's strand orientation is recorded as forward strand[15].
- FAM171B's exact match is recorded as http://identifiers.org/ncbigene/165215[16].
- FAM171B's cytogenetic location is recorded as 2q32.1[17].
- FAM171B's expressed in is recorded as entorhinal cortex[18].
- FAM171B's expressed in is recorded as Brodmann area 46[19].
- FAM171B's expressed in is recorded as endothelial cell[20].
- FAM171B's expressed in is recorded as postcentral gyrus[21].
- FAM171B's expressed in is recorded as Brodmann area 23[22].
- FAM171B's expressed in is recorded as external globus pallidus[23].
- FAM171B's expressed in is recorded as superior frontal gyrus[24].
- FAM171B's expressed in is recorded as medulla oblongata[25].
- FAM171B's expressed in is recorded as cerebellar vermis[26].