uncharacterized LOC128706665 [Homo sapiens]

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Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin. [Clin Exp Ophthalmol. 2020]
Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin.
Goyal S, Singh IR, Vanita V. Clin Exp Ophthalmol. 2020 Apr; 48(3):343-355. Epub 2020 Feb 3.
Novel sequence variants in the MKKS gene cause Bardet-Biedl syndrome with intra- and inter-familial variable phenotypes. [Congenit Anom (Kyoto). 2018]
Novel sequence variants in the MKKS gene cause Bardet-Biedl syndrome with intra- and inter-familial variable phenotypes.
Ullah A, Khalid M, Umair M, Khan SA, Bilal M, Khan S, Ahmad W. Congenit Anom (Kyoto). 2018 Sep; 58(5):173-175. Epub 2017 Dec 22.
Whole-exome sequencing identified compound heterozygous variants in MMKS in a Chinese pedigree with Bardet-Biedl syndrome. [Sci China Life Sci. 2017]
Whole-exome sequencing identified compound heterozygous variants in MMKS in a Chinese pedigree with Bardet-Biedl syndrome.
Qi Z, Shen Y, Fu Q, Li W, Yang W, Xu W, Chu P, Zhang Y, Wang H. Sci China Life Sci. 2017 Jul; 60(7):739-745. Epub 2017 Jun 14.

RefSeq genomic sequence
See the genomic reference sequence for the LOC128706665 gene (NG_009109.3).
RefSeq mRNA
See reference mRNA sequence for the LOC128706665 gene (NM_001394148.2).

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Protein