AC T03321
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ID T03321
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DT 15.05.2000 (created); rio.
DT 20.11.2007 (updated); sba.
CO Copyright (C), QIAGEN.
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FA HOXA13
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SY Hox-1.10.
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OS human, Homo sapiens
OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; primates
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GE G006211 HOXA13; HGNC: HOXA13.
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CL C0006; homeo; 3.1.1.8.13.
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FF mutations within the homeo domain can cause HFG (hand-foot-genital syndrome) [2];
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MX M01292 V$HOXA13_01.
MX M01297 V$HOXA13_02.
MX M01430 V$HOXA13_03.
MX M04341 V$HOXA13_05.
MX M04342 V$HOXA13_06.
MX M07456 V$HOXA913_Q4.
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DR TRANSPATH: MO000027259.
DR PATHODB: MT010471.
DR PATHODB: MT010555.
DR PATHODB: MT010556.
DR PATHODB: MT010557.
DR PATHODB: MT010558.
DR PATHODB: MT010559.
DR UniProtKB: P31271;
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RN [1]; RE0003895.
RX PUBMED: 2574852.
RA Acampora D., D'Esposito M., Faiella A., Pannese M., Migliaccio E., Morelli F., Stornaiuolo A., Nigro V., Simeone A., Boncinelli E.
RT The human HOX gene family
RL Nucleic Acids Res. 17:10385-10402 (1989).
RN [2]; RE0014491.
RX PUBMED: 9020844.
RA Mortlock D. P., Innis J. W.
RT Mutation of HOXA13 in hand-foot-genital syndrome
RL Nat. Genet. 15:179-180 (1997).
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