about
sameAs
P688
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouseMolecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disordersA novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in HESX homeobox 1
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
HESX homeobox 1
@en
type
label
HESX homeobox 1
@en
altLabel
HESX1
@en
Rathke pouch homeobox
@en
hAnf
@en
homeobox expressed in ES cells 1
@en
homeobox protein ANF
@en
prefLabel
HESX homeobox 1
@en
P637
P680
P682
P705
P352
P638
P2888
P31
P352
P637
NP_001362987
NP_001362988
NP_001362989
NP_001362990
XP_005265583
P680
P681
P682
P702
P703
P705
ENSP00000295934
ENSP00000418918
ENSP00000419615
ENSP00000498190