Gene: [02q31/HOXD13] homeo box D13(4I), homologous to mouse Hox-4.9; synpolydactyly (syndactyly type II; MIM:186000); [HOX5 HOX4I ]
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FAG |
See FAM:HOXD/02q31. |
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PAT |
Synpolydactyly is an autosomal dominant limb anomality involving webbing between digits and duplication of fingers. Typical features include fusion between digits III and IV and the presence of an additional finger or toe in between." |
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REF |
GEN,SEQ "Akarsu AN &: Hum Mol Genet, 5, 945-952, 1996 PAT,FOG "Akarsu AN &: J Med Genet, 32, 435-441, 1995 PAT,NOM,FOG "Cross HE &: AJHG, 20, 368-380, 1968 PRO,LOC,FAG "D'Esposito M &: Genomics, 10, 43-50, 1991 PRO,LOC,FAG "Lu-Kuo J &: Genomics, 16, 173-179, 1993 PAT,NOM,FOG "Merlob P, Grunebaum M: J Med Genet, 23, 237-241, 1986 MUT,PAT,SEQ "Muragaki Y &: Science, 272, 548-551, 1996a PAT,MUT "Muragaki Y &: Science, 272, 548-551, 1996b PAT,LOC,LIN "Sarfarazi M &: Hum Mol Genet, 4, 1453-1458, 1995 PAT,FOG "Sayli BS &: J Med Genet, 32, 421-434, 1995 PRO,LOC,FAG "Scott MP &: Cell, 71, 551-553, 1992 MOD,MOU "Zakany J, Duboule D: Nature, 384, 69-71, 1996 |
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KEY |
ont, onc, trc, bone, devd |
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CLA |
coding, basic |
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LOC |
02 q31 |
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MIM |
MIM: 142989 |
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SYN |
HOX5 HOX4I |
