Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 84140
MIM: 613596
HGNC: 25808
Ensembl: ENSG00000170264
Variants:
dbSNP: 84140
ClinVar: 84140
TCGA: ENSG00000170264
COSMIC: FAM161A
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36233334 | 2022 | Interactions between C8orf37 and FAM161A, Two Ciliary Proteins Essential for Photoreceptor Survival. | 1 |
| 36233334 | 2022 | Interactions between C8orf37 and FAM161A, Two Ciliary Proteins Essential for Photoreceptor Survival. | 1 |
| 32938956 | 2020 | Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations. | 11 |
| 33093951 | 2020 | Structural bioinformatics predicts that the Retinitis Pigmentosa-28 protein of unknown function FAM161A is a homologue of the microtubule nucleation factor Tpx2. | 5 |
| 32938956 | 2020 | Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations. | 11 |
| 33093951 | 2020 | Structural bioinformatics predicts that the Retinitis Pigmentosa-28 protein of unknown function FAM161A is a homologue of the microtubule nucleation factor Tpx2. | 5 |
| 25007332 | 2016 | Ocular Phenotype of a Family with FAM161A-associated Retinal Degeneration. | 11 |
| 25007332 | 2016 | Ocular Phenotype of a Family with FAM161A-associated Retinal Degeneration. | 11 |
| 25749990 | 2015 | Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network. | 13 |
| 26113502 | 2015 | Diverse clinical phenotypes associated with a nonsense mutation in FAM161A. | 7 |
| 26246154 | 2015 | Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population. | 10 |
| 26574802 | 2015 | A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa. | 7 |
| 25749990 | 2015 | Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network. | 13 |
| 26113502 | 2015 | Diverse clinical phenotypes associated with a nonsense mutation in FAM161A. | 7 |
| 26246154 | 2015 | Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population. | 10 |
Citation
Dessen P
FAM161A (FAM161 centrosomal protein A)
Atlas Genet Cytogenet Oncol Haematol. 2014-08-01
Online version: http://atlasgeneticsoncology.org/gene/54302/fam161a-(fam161-centrosomal-protein-a)
