Visual system homeobox 2 is a protein that in humans is encoded by the VSX2 gene.[5][6]
References
- 1 2 3 GRCh38: Ensembl release 89: ENSG00000119614 – Ensembl, May 2017
- 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000021239 – Ensembl, May 2017
- ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ↑ McAlpine PJ, Shows TB (July 1990). "Nomenclature for human homeobox genes". Genomics. 7 (3): 460. doi:10.1016/0888-7543(90)90186-X. PMID 1973146.
- ↑ "Entrez Gene: CHX10 ceh-10 homeodomain containing homolog (C. elegans)".
Further reading
- Sanger Center, Washington University Genome Sequencing Center (November 1998). "Toward a complete human genome sequence". Genome Research. 8 (11): 1097–1108. doi:10.1101/gr.8.11.1097. PMID 9847074.
- Ferda Percin E, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, et al. (August 2000). "Human microphthalmia associated with mutations in the retinal homeobox gene CHX10". Nature Genetics. 25 (4): 397–401. doi:10.1038/78071. PMID 10932181. S2CID 9508022.
- Mikkola I, Bruun JA, Holm T, Johansen T (February 2001). "Superactivation of Pax6-mediated transactivation from paired domain-binding sites by dna-independent recruitment of different homeodomain proteins". The Journal of Biological Chemistry. 276 (6): 4109–4118. doi:10.1074/jbc.M008882200. PMID 11069920.
- Bar-Yosef U, Abuelaish I, Harel T, Hendler N, Ofir R, Birk OS (September 2004). "CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds". Human Genetics. 115 (4): 302–309. doi:10.1007/s00439-004-1154-2. PMID 15257456. S2CID 28981190.
- Dorval KM, Bobechko BP, Ahmad KF, Bremner R (March 2005). "Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1". The Journal of Biological Chemistry. 280 (11): 10100–10108. doi:10.1074/jbc.M412676200. PMID 15647262.
- Kuiper H, Spötter A, Williams JL, Distl O, Drögemüller C (2005). "Physical mapping of CHX10, ALDH6A1, and ABCD4 on bovine chromosome 10q34". Cytogenetic and Genome Research. 109 (4): 533. doi:10.1159/000084217. PMID 15909363.
- Dorval KM, Bobechko BP, Fujieda H, Chen S, Zack DJ, Bremner R (January 2006). "CHX10 targets a subset of photoreceptor genes". The Journal of Biological Chemistry. 281 (2): 744–751. doi:10.1074/jbc.M509470200. PMID 16236706.
- Faiyaz-Ul-Haque M, Zaidi SH, Al-Mureikhi MS, Peltekova I, Tsui LC, Teebi AS (August 2007). "Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar". Clinical Genetics. 72 (2): 164–166. doi:10.1111/j.1399-0004.2007.00846.x. PMID 17661825. S2CID 6218901.