FAM169A
protein-coding gene in the species Homo sapiens
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FAM169A
Summary
FAM169A is a gene[1].
Key Facts
- FAM169A's instance of is recorded as gene[2].
- FAM169A is a type of protein-coding gene[3].
- FAM169A's HomoloGene ID is recorded as 52656[4].
- FAM169A's genomic start is recorded as 74777574[5].
- FAM169A's genomic start is recorded as 74073399[6].
- FAM169A's genomic end is recorded as 74162776[7].
- FAM169A's genomic end is recorded as 74866966[8].
- FAM169A's ortholog is recorded as Fam169a[9].
- FAM169A's ortholog is recorded as Fam169a[10].
- FAM169A's encodes is recorded as Family with sequence similarity 169 member A[11].
- FAM169A's found in taxon is recorded as Homo sapiens[12].
- FAM169A's chromosome is recorded as human chromosome 5[13].
- FAM169A's strand orientation is recorded as reverse strand[14].
- FAM169A's exact match is recorded as http://identifiers.org/ncbigene/26049[15].
- FAM169A's cytogenetic location is recorded as 5q13.3[16].
- FAM169A's expressed in is recorded as caput epididymis[17].
- FAM169A's expressed in is recorded as corpus epididymis[18].
- FAM169A's expressed in is recorded as lateral nuclear group of thalamus[19].
- FAM169A's expressed in is recorded as endothelial cell[20].
- FAM169A's expressed in is recorded as postcentral gyrus[21].
- FAM169A's expressed in is recorded as optic nerve[22].
- FAM169A's expressed in is recorded as entorhinal cortex[23].
- FAM169A's expressed in is recorded as pars compacta[24].
- FAM169A's expressed in is recorded as superior vestibular nucleus[25].
- FAM169A's expressed in is recorded as Brodmann area 23[26].