DLX6
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| Location (UCSC) | Chr 7: 97.01 – 97.01 Mb | Chr 6: 6.86 – 6.87 Mb | |||||||
| PubMed search | [3] | [4] | |||||||
| View/Edit Human | View/Edit Mouse |
Homeobox protein DLX-6 is a protein that in humans is encoded by the DLX6 gene.[5][6]
This gene encodes a member of a homeobox transcription factor gene family similar to the
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000006377 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029754 – 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.
- PMID 7907794.
- ^ a b "Entrez Gene: DLX6 distal-less homeobox 6".
Further reading
- Crackower MA, Scherer SW, Rommens JM, et al. (1997). "Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development". Hum. Mol. Genet. 5 (5): 571–9. PMID 8733122.
- Charité J, McFadden DG, Merlo G, et al. (2001). "Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer". Genes Dev. 15 (22): 3039–49. PMID 11711438.
- Depew MJ, Lufkin T, Rubenstein JL (2002). "Specification of jaw subdivisions by Dlx genes". Science. 298 (5592): 381–5. S2CID 10274300.
- 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): 16899–903. PMID 12477932.
- Nabi R, Zhong H, Serajee FJ, Huq AH (2004). "No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism". Am. J. Med. Genet. B Neuropsychiatr. Genet. 119 (1): 98–101. S2CID 39985829.
- Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7". Nature. 424 (6945): 157–64. PMID 12853948.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. PMID 14702039.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. PMID 15489334.
- Schüle B, Li HH, Fisch-Kohl C, et al. (2007). "DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency". Am. J. Hum. Genet. 81 (3): 492–506. PMID 17701895.
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