chromosome 9 open reading frame 96, isoform CRA_f [Homo sapiens]

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Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limb. [Clin Genet. 2019]
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limb.
Umair M, Bilal M, Ali RH, Alhaddad B, Ahmad F, Abdullah, Haack TB, Alfadhel M, Ansar M, Meitinger T, et al. Clin Genet. 2019 Aug; 96(2):134-139. Epub 2019 Apr 22.
Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. [Mol Cell Proteomics. 2014]
Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics.
Fagerberg L, Hallström BM, Oksvold P, Kampf C, Djureinovic D, Odeberg J, Habuka M, Tahmasebpoor S, Danielsson A, Edlund K, et al. Mol Cell Proteomics. 2014 Feb; 13(2):397-406. Epub 2013 Dec 5.
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. [Proc Natl Acad Sci U S A. 2013]
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Desch KC, Ozel AB, Siemieniak D, Kalish Y, Shavit JA, Thornburg CD, Sharathkumar AA, McHugh CP, Laurie CC, Crenshaw A, et al. Proc Natl Acad Sci U S A. 2013 Jan 8; 110(2):588-93. Epub 2012 Dec 24.

RefSeq protein
See the reference protein sequence for serine/threonine kinase-like domain-containing protein STKLD1 (NP_714921.4).

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