TRANSFAC-Logo

TRANSFAC FACTOR TABLE, Release 2017.2 - public - 2017-06-30, (C) QIAGEN


AC T03337 XX ID T03337 XX DT 17.05.2000 (created); rio. DT 20.06.2014 (updated); pro. CO Copyright (C), QIAGEN. XX FA HOXA13 XX SY Hox-1.10. XX OS mouse, Mus musculus OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; rodentia; myomorpha; muridae; murinae XX GE G006212 Hoxa13. XX CL C0006; homeo; 3.1.1.8.13. XX SF phenotype of hypodactyly (hd) mice: Hd/+ mice have a shortened digit 1 on all four limbs but are otherwise normal and fertile whereas Hd/Hd animals usually die in utero - those that are born have a single digit on each limb and are infertile [1]; XX FF hypodactyly (Hd) is caused by a deletion in the first exon and is also observed in HOXD13 deficient mice [1]; XX IN T03388 meis1-a; mouse, Mus musculus. IN T03389 meis1-b; mouse, Mus musculus. XX MX M01292 V$HOXA13_01. MX M01297 V$HOXA13_02. MX M01430 V$HOXA13_03. MX M07456 V$HOXA913_Q4. XX BS R62480. BS R62487. BS R62488. BS R18926. BS R18927. BS R18928. BS R18930. BS R18929. XX DR TRANSPATH: MO000027275. DR PATHODB: MT010472. DR UniProtKB: Q62424; XX RN [1]; RE0014509. RX PUBMED: 8673126. RA Mortlock D. P., Post L. C., Innis J. W. RT The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation RL Nat. Genet. 13:284-289 (1996). RN [2]; RE0064941. RX PUBMED: 15617687. RA Williams T. M., Williams M. E., Innis J. W. RT Range of HOX/TALE superclass associations and protein domain requirements for HOXA13:MEIS interaction. RL Dev. Biol. 277:457-471 (2005). XX //