DLX6

DLX6
Identifiers
Aliases	DLX6, distal-less homeobox 6
External IDs	OMIM: 600030 MGI: 101927 HomoloGene: 87855 GeneCards: DLX6
Gene location (Human)
Chr.	Chromosome 7 (human)[1]
End	97,011,040 bp[1]
Gene location (Mouse)
Chr.	Chromosome 6 (mouse)[2]
End	6,868,568 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity; • sequence-specific DNA binding; • DNA binding; • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific; • GO:0000980 RNA polymerase II cis-regulatory region sequence-specific DNA binding;
Cellular component	• cell nucleus;
Biological process	• skeletal system development; • regulation of transcription, DNA-templated; • nervous system development; • embryonic limb morphogenesis; • epithelial cell differentiation; • inner ear morphogenesis; • anatomical structure formation involved in morphogenesis; • positive regulation of epithelial cell proliferation; • palate development; • head development; • multicellular organism development; • regulation of transcription from RNA polymerase II promoter; • cell differentiation; • positive regulation of transcription from RNA polymerase II promoter;
	Sources:Amigo / QuickGO
Orthologs
	1750
	13396
	ENSG00000006377
	ENSMUSG00000029754
	P56179
	P70397
	NM_005222
	NM_010057
	NP_005213
	NP_034187
	Wikidata
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 Drosophila distal-less gene. This family has at least six members that encode proteins with roles in forebrain and craniofacial development. This gene is in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7.[6]

References

GRCh38: Ensembl release 89: ENSG00000006377 - Ensembl, May 2017
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.
Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K, et al. (Apr 1994). "Cloning and characterization of two members of the vertebrate Dlx gene family". Proc Natl Acad Sci U S A. 91 (6): 2250–4. doi:10.1073/pnas.91.6.2250. PMC 43348. PMID 7907794.
"Entrez Gene: DLX6 distal-less homeobox 6".

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. doi:10.1093/hmg/5.5.571. 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. doi:10.1101/gad.931701. PMC 312822. PMID 11711438.
Depew MJ, Lufkin T, Rubenstein JL (2002). "Specification of jaw subdivisions by Dlx genes". Science. 298 (5592): 381–5. doi:10.1126/science.1075703. PMID 12193642.
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. doi:10.1073/pnas.242603899. PMC 139241. 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. doi:10.1002/ajmg.b.10012. PMID 12707945.
Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7". Nature. 424 (6945): 157–64. doi:10.1038/nature01782. 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. doi:10.1038/ng1285. 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. doi:10.1101/gr.2596504. PMC 528928. 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. doi:10.1086/520063. PMC 1950824. PMID 17701895.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000006377 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000029754 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid7907794-5] Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K, et al. (Apr 1994). "Cloning and characterization of two members of the vertebrate Dlx gene family". Proc Natl Acad Sci U S A. 91 (6): 2250–4. doi:10.1073/pnas.91.6.2250. PMC 43348. PMID 7907794.

[entrez-6] "Entrez Gene: DLX6 distal-less homeobox 6".

DLX6

References

Further reading