FAM161A
protein-coding gene in the species Homo sapiens
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FAM161A
Summary
FAM161A is a gene[1].
Key Facts
- FAM161A's instance of is recorded as gene[2].
- FAM161A is a type of protein-coding gene[3].
- FAM161A's HomoloGene ID is recorded as 19131[4].
- FAM161A's genomic start is recorded as 62051989[5].
- FAM161A's genomic start is recorded as 61824848[6].
- FAM161A's genomic end is recorded as 61854143[7].
- FAM161A's genomic end is recorded as 62081278[8].
- FAM161A's ortholog is recorded as Fam161a[9].
- FAM161A's ortholog is recorded as Fam161a[10].
- FAM161A's ortholog is recorded as fam161a[11].
- FAM161A's encodes is recorded as FAM161 centrosomal protein A[12].
- FAM161A's found in taxon is recorded as Homo sapiens[13].
- FAM161A's chromosome is recorded as human chromosome 2[14].
- FAM161A's genetic association is recorded as retinitis pigmentosa 28[15].
- FAM161A's strand orientation is recorded as reverse strand[16].
- FAM161A's exact match is recorded as http://identifiers.org/ncbigene/84140[17].
- FAM161A's cytogenetic location is recorded as 2p15[18].
- FAM161A's expressed in is recorded as retinal pigment epithelium[19].
- FAM161A's expressed in is recorded as sperm[20].
- FAM161A's expressed in is recorded as secondary oocyte[21].
- FAM161A's expressed in is recorded as bronchial epithelial cell[22].
- FAM161A's expressed in is recorded as testicle[23].
- FAM161A's expressed in is recorded as ventricular zone[24].
- FAM161A's expressed in is recorded as gonad[25].
- FAM161A's expressed in is recorded as ganglionic eminence[26].