protein fantom isoform X7 [Homo sapiens]

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Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family. [Reprod Sci. 2022]
Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family.
Zhang P, Wu B, Wang Y, Ren Y, Li G, Qan Y, Lei C, Wang H. Reprod Sci. 2022 Aug; 29(8):2200-2207. Epub 2022 Mar 1.
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS). [Genet Epidemiol. 2019]
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS).
Javanrouh N, Soltanian AR, Tapak L, Azizi F, Ott J, Daneshpour MS. Genet Epidemiol. 2019 Apr; 43(3):342-351. Epub 2018 Dec 30.
Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population. [Chin Med J (Engl). 2018]
Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population.
Hu M, Wang TM, Dong YY, She QY, Gao S, Liu DX, Deng YH. Chin Med J (Engl). 2018 Dec 20; 131(24):3022-3024.

RefSeq genomic sequence
See the genomic reference sequence for the RPGRIP1L gene (NG_008991.2).
RefSeq mRNA
See reference mRNA sequence for the RPGRIP1L gene (XM_054379960.1).
RefSeq protein isoforms
See 50 reference sequence protein isoforms for the RPGRIP1L gene.

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Protein