RecName: Full=Protein FAM161A

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Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations. [Sci Rep. 2020]
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations.
Beryozkin A, Khateb S, Idrobo-Robalino CA, Khan MI, Cremers FPM, Obolensky A, Hanany M, Mezer E, Chowers I, Newman H, et al. Sci Rep. 2020 Sep 16; 10(1):15156. Epub 2020 Sep 16.
A helical inner scaffold provides a structural basis for centriole cohesion. [Sci Adv. 2020]
A helical inner scaffold provides a structural basis for centriole cohesion.
Le Guennec M, Klena N, Gambarotto D, Laporte MH, Tassin AM, van den Hoek H, Erdmann PS, Schaffer M, Kovacik L, Borgers S, et al. Sci Adv. 2020 Feb; 6(7):eaaz4137. Epub 2020 Feb 14.
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa. [Invest Ophthalmol Vis Sci. 2015]
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa.
Van Schil K, Klevering BJ, Leroy BP, Pott JW, Bandah-Rozenfeld D, Zonneveld-Vrieling MN, Sharon D, den Hollander AI, Cremers FP, De Baere E, et al. Invest Ophthalmol Vis Sci. 2015 Nov; 56(12):7418-26.

RefSeq genomic sequence
See the genomic reference sequence for the FAM161A gene (NG_028125.2).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the FAM161A gene.

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Q3B820 [Domain Mapping of Disease Mut...]
Q3B820
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein