about
P688
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephalyDirect interaction of geminin and Six3 in eye developmentMutations in the human SIX3 gene in holoprosencephaly are loss of functionSix3 and Six6 activity is modulated by members of the groucho familyRegulation of a remote Shh forebrain enhancer by the Six3 homeoprotein
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in SIX homeobox 3
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
SIX homeobox 3
@en
type
label
SIX homeobox 3
@en
altLabel
SIX3
@en
homeobox protein SIX3
@en
sine oculis homeobox homolog 3
@en
sine oculis homeobox-like protein 3
@en
truncated SIX3
@en
prefLabel
SIX homeobox 3
@en
P680
P681
P682
P352
P637
P279
P31
P352
P637
P680
P682
P702
P703
P705
ENSP00000260653