Homo sapiens cytochrome P450 family 7 subfamily B member 1 (CYP7B1), R - Nucleotide

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Pediatric Genetic Cholestatic Liver Disease Overview. [GeneReviews(®). 1993]
Pediatric Genetic Cholestatic Liver Disease Overview.
Amendola M, Squires JE. GeneReviews(®). 1993-2024. 2022 Sep 15 [updated 2023 May 25]
Physical and functional interactome atlas of human receptor tyrosine kinases. [EMBO Rep. 2022]
Physical and functional interactome atlas of human receptor tyrosine kinases.
Salokas K, Liu X, Öhman T, Chowdhury I, Gawriyski L, Keskitalo S, Varjosalo M. EMBO Rep. 2022 Jun 7; 23(6):e54041. Epub 2022 Apr 5.
Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations. [Genes (Basel). 2021]
Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations.
Theuriet J, Pegat A, Leblanc P, Vukusic S, Cazeneuve C, Millecamps S, Banneau G, Guillaud-Bataille M, Bernard E. Genes (Basel). 2021 Nov 25; 12(12). Epub 2021 Nov 25.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the CYP7B1 gene.

Protein
Protein sequence from Nucleotide coding region
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Nucleotide