schwannomin-interacting protein 1 isoform 5 [Homo sapiens]

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Homozygous nonsense mutation in SCHIP1/IQCJ-SCHIP1 causes a neurodevelopmental brain malformation syndrome. [Clin Genet. 2018]
Homozygous nonsense mutation in SCHIP1/IQCJ-SCHIP1 causes a neurodevelopmental brain malformation syndrome.
Elsaid MF, Chalhoub N, Ben-Omran T, Kamel H, Al Mureikhi M, Ibrahim K, Elizabeth Ross M, Abdel Aleem AK. Clin Genet. 2018 Feb; 93(2):387-391. Epub 2017 Dec 20.
Assignment of the schwannomin-interacting protein 1 (SCHIP1) gene to human chromosome band 3q25 by in situ hybridization and with somatic cell hybrids. [Cytogenet Cell Genet. 2001]
Assignment of the schwannomin-interacting protein 1 (SCHIP1) gene to human chromosome band 3q25 by in situ hybridization and with somatic cell hybrids.
Goutebroze L, Der Sarkissian H, Brault E, Thomas G. Cytogenet Cell Genet. 2001; 94(1-2):96-7.
Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape. [PLoS Genet. 2016]
Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape.
Cole JB, Manyama M, Kimwaga E, Mathayo J, Larson JR, Liberton DK, Lukowiak K, Ferrara TM, Riccardi SL, Li M, et al. PLoS Genet. 2016 Aug; 12(8):e1006174. Epub 2016 Aug 25.

RefSeq mRNA
See reference mRNA sequence for the SCHIP1 gene (NM_001394286.1).
RefSeq protein isoforms
See 31 reference sequence protein isoforms for the SCHIP1 gene.

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Protein