TMEM169
protein-coding gene in the species Homo sapiens
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TMEM169
Summary
TMEM169 is a gene[1].
Key Facts
- TMEM169's instance of is recorded as gene[2].
- TMEM169 is a type of protein-coding gene[3].
- TMEM169's HomoloGene ID is recorded as 16305[4].
- TMEM169's genomic start is recorded as 216081866[5].
- TMEM169's genomic start is recorded as 216946589[6].
- TMEM169's genomic end is recorded as 216102783[7].
- TMEM169's genomic end is recorded as 216967506[8].
- TMEM169's ortholog is recorded as Tmem169[9].
- TMEM169's ortholog is recorded as Tmem169[10].
- TMEM169's ortholog is recorded as tmem169b[11].
- TMEM169's encodes is recorded as Transmembrane protein 169[12].
- TMEM169's found in taxon is recorded as Homo sapiens[13].
- TMEM169's chromosome is recorded as human chromosome 2[14].
- TMEM169's strand orientation is recorded as forward strand[15].
- TMEM169's exact match is recorded as http://identifiers.org/ncbigene/92691[16].
- TMEM169's cytogenetic location is recorded as 2q35[17].
- TMEM169's expressed in is recorded as buccal mucosa cell[18].
- TMEM169's expressed in is recorded as ganglionic eminence[19].
- TMEM169's expressed in is recorded as secondary oocyte[20].
- TMEM169's expressed in is recorded as prefrontal cortex[21].
- TMEM169's expressed in is recorded as stromal cell of endometrium[22].
- TMEM169's expressed in is recorded as Brodmann area 9[23].
- TMEM169's expressed in is recorded as ventricular zone[24].
- TMEM169's expressed in is recorded as cerebellar cortex[25].
- TMEM169's expressed in is recorded as cerebellar hemisphere[26].