호모 사피엔스 종의 단백질 코드 유전자
시각계 호메오박스2 는 VSX2 [5] [6] 단백질 이다.
레퍼런스 추가 정보 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. 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. 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 Commons에는 Vsx2
