hCG2040102, isoform CRA_a [Homo sapiens]

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Novel mutations in HSF4 cause congenital cataracts in Chinese families. [BMC Med Genet. 2018]
Novel mutations in HSF4 cause congenital cataracts in Chinese families.
Cao Z, Zhu Y, Liu L, Wu S, Liu B, Zhuang J, Tong Y, Chen X, Xie Y, Nie K, et al. BMC Med Genet. 2018 Aug 24; 19(1):150. Epub 2018 Aug 24.
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family. [Eye (Lond). 2018]
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family.
Berry V, Pontikos N, Moore A, Ionides ACW, Plagnol V, Cheetham ME, Michaelides M. Eye (Lond). 2018 Apr; 32(4):806-812. Epub 2017 Dec 15.
High HSF4 expression is an independent indicator of poor overall survival and recurrence free survival in patients with primary colorectal cancer. [IUBMB Life. 2017]
High HSF4 expression is an independent indicator of poor overall survival and recurrence free survival in patients with primary colorectal cancer.
Yang Y, Jin L, Zhang J, Wang J, Zhao X, Wu G, Yao H, Zhang Z. IUBMB Life. 2017 Dec; 69(12):956-961. Epub 2017 Nov 13.

RefSeq genomic sequence
See the genomic reference sequence for the HSF4 gene (NG_009294.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the HSF4 gene.

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Protein