DLX3 (distal-less homeobox 3)

2007-09-01  

Identity

HGNC
LOCATION
17q21.33
LOCUSID
ALIAS
AI4,TDO

Other Information

Locus ID:

NCBI: 1747
MIM: 600525
HGNC: 2916
Ensembl: ENSG00000064195

Variants:

dbSNP: 1747
ClinVar: 1747
TCGA: ENSG00000064195
COSMIC: DLX3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000064195ENST00000434704O60479
ENSG00000064195ENST00000512495F8VXG1

Expression (GTEx)

0
10
20
30
40
50
60
70
80
90

References

Pubmed IDYearTitleCitations
156662992005DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism.38
117928342002Genomic structure and functional control of the Dlx3-7 bigene cluster.26
184926702008Molecular consequences of a frameshifted DLX3 mutant leading to Tricho-Dento-Osseous syndrome.24
192826652009Homeodomain protein Dlx3 induces phosphorylation-dependent p63 degradation.22
189786782008Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.21
194532612009High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.20
162475492006PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses.17
182031972008DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome.15
164679782006Gene expression of runx2, Osterix, c-fos, DLX-3, DLX-5, and MSX-2 in dental follicle cells during osteogenic differentiation in vitro.14
154541072004Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome.13

Citation

Dessen P

DLX3 (distal-less homeobox 3)

Atlas Genet Cytogenet Oncol Haematol. 2007-09-01

Online version: http://atlasgeneticsoncology.org/gene/49723/dlx3