about
P688
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractAltered growth and branching patterns in synpolydactyly caused by mutations in HOXD13Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese familiesA homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Homeobox D13
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Homeobox D13
@en
type
label
Homeobox D13
@en
altLabel
HOXD13
@en
homeo box 4I
@en
homeo box D13
@en
homeobox protein Hox-4I
@en
homeobox protein Hox-D13
@en
synpolydactyly
@en
prefLabel
Homeobox D13
@en
P527
P637
P680
P682
P352
P31
P352
P637
XP_011509370
XP_011509371
P680
P681
P682
P702
P703
P705
ENSP00000376322