Homo sapiens protein kinase-like protein SgK493, mRNA (cDNA clone IMAG - Nucleotide

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Identification of bone mineral density associated genes with shared genetic architectures across multiple tissues: Functional insights for EPDR1, PKDCC, and SPTBN1. [PLoS One. 2024]
Identification of bone mineral density associated genes with shared genetic architectures across multiple tissues: Functional insights for EPDR1, PKDCC, and SPTBN1.
Jung J, Wu Q. PLoS One. 2024; 19(4):e0300535. Epub 2024 Apr 29.
A common cis-regulatory variant impacts normal-range and disease-associated human facial shape through regulation of PKDCC during chondrogenesis. [Elife. 2024]
A common cis-regulatory variant impacts normal-range and disease-associated human facial shape through regulation of PKDCC during chondrogenesis.
Mohammed J, Arora N, Matthews HS, Hansen K, Bader M, Walsh S, Shaffer JR, Weinberg SM, Swigut T, Claes P, et al. Elife. 2024 Mar 14; 13. Epub 2024 Mar 14.
Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China. [BMC Med Genomics. 2023]
Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China.
Yan L, Cao J, Zhang Y, Liu Y, Zou J, Lou B, Zhuang D, Li H. BMC Med Genomics. 2023 Aug 17; 16(1):190. Epub 2023 Aug 17.