From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Visual system homeobox 2 is a
protein that in humans is encoded by the VSX2
gene .
[5]
[6]
References
Further reading
Sanger Centre, The; Washington University Genome Sequencing Centre, The (1999).
"Toward a complete human genome sequence" . Genome Res . 8 (11): 1097–1108.
doi :
10.1101/gr.8.11.1097 .
PMID
9847074 .
Ferda Percin E, Ploder LA, Yu JJ, et al. (2000). "Human microphthalmia associated with mutations in the retinal homeobox gene CHX10". Nat. Genet . 25 (4): 397–401.
doi :
10.1038/78071 .
PMID
10932181 .
S2CID
9508022 .
Mikkola I, Bruun JA, Holm T, Johansen T (2001).
"Superactivation of Pax6-mediated transactivation from paired domain-binding sites by dna-independent recruitment of different homeodomain proteins" . J. Biol. Chem . 276 (6): 4109–4118.
doi :
10.1074/jbc.M008882200 .
PMID
11069920 .
Strausberg RL, Feingold EA, Grouse LH, et al. (2003).
"Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" . Proc. Natl. Acad. Sci. U.S.A . 99 (26): 16899–16903.
Bibcode :
2002PNAS...9916899M .
doi :
10.1073/pnas.242603899 .
PMC
139241 .
PMID
12477932 .
Heilig R, Eckenberg R, Petit JL, et al. (2003).
"The DNA sequence and analysis of human chromosome 14" . Nature . 421 (6923): 601–607.
Bibcode :
2003Natur.421..601H .
doi :
10.1038/nature01348 .
PMID
12508121 .
Bar-Yosef U, Abuelaish I, Harel T, et al. (2005). "CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds". Hum. Genet . 115 (4): 302–309.
doi :
10.1007/s00439-004-1154-2 .
PMID
15257456 .
S2CID
28981190 .
Dorval KM, Bobechko BP, Ahmad KF, Bremner R (2005).
"Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1" . J. Biol. Chem . 280 (11): 10100–10108.
doi :
10.1074/jbc.M412676200 .
PMID
15647262 .
Kuiper H, Spötter A, Williams JL, et al. (2005).
"Physical mapping of CHX10, ALDH6A1, and ABCD4 on bovine chromosome 10q34" . Cytogenet. Genome Res . 109 (4): 533.
doi :
10.1159/000084217 .
PMID
15909363 .
Dorval KM, Bobechko BP, Fujieda H, et al. (2006).
"CHX10 targets a subset of photoreceptor genes" . J. Biol. Chem . 281 (2): 744–751.
doi :
10.1074/jbc.M509470200 .
PMID
16236706 .
Faiyaz-Ul-Haque M, Zaidi SH, Al-Mureikhi MS, et al. (2007). "Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar". Clin. Genet . 72 (2): 164–166.
doi :
10.1111/j.1399-0004.2007.00846.x .
PMID
17661825 .
S2CID
6218901 .
Wikimedia Commons has media related to
Vsx2 .