AC T03991
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ID T03991
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DT 03.11.2000 (created); rio.
DT 11.01.2016 (updated); mkl.
CO Copyright (C), QIAGEN.
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FA Dlx-3
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SY distalless homeobox 3; dlx-3; dlx3.
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OS human, Homo sapiens
OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; primates
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GE G002021 DLX3; HGNC: DLX3.
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HO Dll (Drosophila) T02005.
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CL C0006; homeo; 3.1.2.5.3.
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SF 98% overall identity to murine Dlx-3 [1];
SF closely linked to the Dlx-4 T03992 gene [1] [2];
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CP placenta [1].
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FF associated with (TDO) tricho-dento-osseous syndrome which includes taurodontism, enamel hypoplasia, hair anomalies, increased thickness and density of the cranial bones [1];
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MX M01400 V$DLX3_01.
MX M04301 V$DLX3_04.
MX M07603 V$DLX3_Q3.
MX M07278 V$DLX3_Q6.
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BS R19707.
BS R62932.
BS R62935.
BS R62937.
BS R21276.
BS R62929.
BS R62930.
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DR TRANSPATH: MO000027901.
DR PATHODB: MT010596.
DR UniProtKB: O60479;
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RN [1]; RE0015265.
RX PUBMED: 9467018.
RA Price J. A., Bowden D. W., Wright J. T., Pettenati M. J., Hart T. C.
RT Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
RL Hum. Mol. Genet. 7:563-569 (1998).
RN [2]; RE0015266.
RX PUBMED: 8975708.
RA Nakamura S., Stock D. W., Wydner K. L., Bollekens J. A., Takeshita K., Nagai B. M., Chiba S., Kitamura T., Freeland T. M., Zhao Z., Minowada J., Lawrence J. B., Weiss K. M., Ruddle F. H.
RT Genomic analysis of a new mammalian distal-less gene: Dlx7
RL Genomics 38:314-324 (1996).
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