FAM161A
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[11]
- Cytogenetic location
- 2p15[14]
- Expressed in
- retinal pigment epithelium, sperm, secondary oocyte, bronchial epithelial cell, testicle, ventricular zone, gonad, ganglionic eminence, right testis, left testis[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- retinitis pigmentosa 28[12]
- HomoloGene ID
- 19131[3]
- Strand orientation
- reverse strand[13]
🏷️ Also known as
en FAM161A
en FAM161A, centrosomal protein
en FAM161 centrosomal protein A
en family with sequence similarity 161 member A
en RP28
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000170264
- Ensembl transcript ID
- ENST00000496369, ENST00000307507, ENST00000404929, ENST00000405894, ENST00000418113, ENST00000456262, ENST00000478494
- Entrez Gene ID
- 84140
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11f10592_p
- HGNC ID
- 25808
- HGNC gene symbol
- FAM161A
- OMIM ID
- 613596
- RefSeq RNA ID
- NM_001201543, NM_032180, NR_037710, XR_001738972, XR_001738975, XM_047445962, XR_007082540
- UMLS CUI
- C2681489
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