about
P688
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humansEvidence of a sex-dependent association between the MSX1 locus and nonsyndromic cleft lip with or without cleft palate in the Chilean populationA nonsense mutation in MSX1 causes Witkop syndromeHomeobox Msx1 interacts with p53 tumor suppressor and inhibits tumor growth by inducing apoptosisMSX1 and TGFB3 contribute to clefting in South AmericaA human MSX1 homeodomain missense mutation causes selective tooth agenesis
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Msh homeobox 1
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Msh homeobox 1
@en
type
label
Msh homeobox 1
@en
altLabel
MSX1
@en
homeobox 7
@en
homeobox protein Hox-7
@en
homeobox protein MSX-1
@en
msh homeo box 1
@en
msh homeobox 1-like protein
@en
msh homeobox homolog 1
@en
prefLabel
Msh homeobox 1
@en
P527
P680
P681
P682
P352
P486
P637
P638
P31
P352
P486
P637
P680
P682
P702
P703
P705
ENSP00000372170