Homo sapiens SIX homeobox 6 (SIX6), RefSeqGene on chromosome 14

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Lack of association between SIX1/SIX6 locus polymorphisms and pseudoexfoliation syndrome in a population from the Republic of Korea. [Medicine (Baltimore). 2022]
Lack of association between SIX1/SIX6 locus polymorphisms and pseudoexfoliation syndrome in a population from the Republic of Korea.
Lee YC, Lee MY, Shin HY. Medicine (Baltimore). 2022 Dec 30; 101(52):e31542.
Mutually exclusive epigenetic modification on SIX6 with hypermethylation for precancerous stage and metastasis emergence tracing. [Signal Transduct Target Ther. ...]
Mutually exclusive epigenetic modification on SIX6 with hypermethylation for precancerous stage and metastasis emergence tracing.
Dong S, Yang Z, Xu P, Zheng W, Zhang B, Fu F, Mao Z, Yuan J, Chen H, Yu W. Signal Transduct Target Ther. 2022 Jul 6; 7(1):208. Epub 2022 Jul 6.
Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. [Mol Vis. 2022]
Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia.
Panagiotou ES, Fernandez-Fuentes N, Farraj LA, McKibbin M, Elçioglu NH, Jafri H, Cerman E, Parry DA, Logan CV, Johnson CA, et al. Mol Vis. 2022; 28:57-69. Epub 2022 May 17.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide