Homo sapiens cDNA FLJ32604 fis, clone STOMA1000133

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Whole exome sequencing identified FAM149A as a plausible causative gene for congenital hereditary endothelial dystrophy, affecting Nrf2-Antioxidant signaling upon oxidative stress. [Free Radic Biol Med. 2021]
Whole exome sequencing identified FAM149A as a plausible causative gene for congenital hereditary endothelial dystrophy, affecting Nrf2-Antioxidant signaling upon oxidative stress.
Zhang J, Dai Y, Wu D, Li Y, Xu J. Free Radic Biol Med. 2021 Sep; 173:117-124. Epub 2021 Jul 23.
TNF-α inhibits glucocorticoid receptor-induced gene expression by reshaping the GR nuclear cofactor profile. [Proc Natl Acad Sci U S A. 2019]
TNF-α inhibits glucocorticoid receptor-induced gene expression by reshaping the GR nuclear cofactor profile.
Dendoncker K, Timmermans S, Vandewalle J, Eggermont M, Lempiäinen J, Paakinaho V, Van Hamme E, Dewaele S, Vandevyver S, Ballegeer M, et al. Proc Natl Acad Sci U S A. 2019 Jun 25; 116(26):12942-12951. Epub 2019 Jun 10.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing. [Proc Natl Acad Sci U S A. 2017]
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing.
Fei T, Chen Y, Xiao T, Li W, Cato L, Zhang P, Cotter MB, Bowden M, Lis RT, Zhao SG, et al. Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26):E5207-E5215. Epub 2017 Jun 13.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the FAM149A gene.

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Nucleotide