S phase cyclin A-associated protein in the endoplasmic reticulum isofo - Protein

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Delineating the expanding phenotype associated with SCAPER gene mutation. [Am J Med Genet A. 2019]
Delineating the expanding phenotype associated with SCAPER gene mutation.
Fasham J, Arno G, Lin S, Xu M, Carss KJ, Hull S, Lane A, Robson AG, Wenger O, Self JE, et al. Am J Med Genet A. 2019 Aug; 179(8):1665-1671. Epub 2019 Jun 13.
Homozygous variants in the gene SCAPER cause syndromic intellectual disability. [Am J Med Genet A. 2019]
Homozygous variants in the gene SCAPER cause syndromic intellectual disability.
Kahrizi K, Huber M, Galetzka D, Dewi S, Schröder J, Weis E, Kariminejad A, Fattahi Z, Ropers HH, Schweiger S, et al. Am J Med Genet A. 2019 Jul; 179(7):1214-1225. Epub 2019 May 9.
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome. [Eur J Hum Genet. 2019]
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome.
Wormser O, Gradstein L, Yogev Y, Perez Y, Kadir R, Goliand I, Sadka Y, El Riati S, Flusser H, Nachmias D, et al. Eur J Hum Genet. 2019 Jun; 27(6):928-940. Epub 2019 Feb 5.

RefSeq mRNA
See reference mRNA sequence for the SCAPER gene (XM_011521656.4).
RefSeq protein isoforms
See 52 reference sequence protein isoforms for the SCAPER gene.

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Protein