Sequence Detail

ID/Version

Q8QZV6 (UniProt | EBI)

Last sequence update: 2022-12-14
Last annotation update: 2025-06-18

Sequence description from provider

RecName: Full=Protein FAM161A {ECO:0000305};

Provider

SWISS-PROT

Sequence

Polypeptide 475 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Fam161a	family with sequence similarity 161, member A	35	100	3	10

Sequence references in MGI

J:169188 Bandah-Rozenfeld D, et al., Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa. Am J Hum Genet. 2010 Sep 10;87(3):382-91
J:169189 Langmann T, et al., Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa. Am J Hum Genet. 2010 Sep 10;87(3):376-81
J:188002 Zach F, et al., The retinitis pigmentosa 28 protein FAM161A is a novel ciliary protein involved in intermolecular protein interaction and microtubule association. Hum Mol Genet. 2012 Nov 1;21(21):4573-86
J:188915 Di Gioia SA, et al., FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies. Hum Mol Genet. 2012 Dec 1;21(23):5174-84