about
sameAs
P688
CHARGE syndrome: an updateLimb anomalies in patients with CHARGE syndrome: an expansion of the phenotypeMutations in a new member of the chromodomain gene family cause CHARGE syndromeCHARGE syndrome: report of 47 cases and reviewCHD8 interacts with CHD7, a protein which is mutated in CHARGE syndromeCHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 geneImmunological abnormalities in CHARGE syndrome
P921
Q24297162-D6532FB5-16D6-44B1-95EE-41D41112E913Q24297781-C029415F-7259-4F68-AAAF-AA9F7537A129Q24300737-18EF7768-5E27-403A-89A7-D5959D47ACF8Q24309120-A129A145-9F2E-42CA-ADE5-8A4F643E8F2FQ24311335-08FF477B-549E-4B0B-94C7-85B10EAE5E6FQ24322458-52489665-A55F-4EC9-A938-737BEE9DB7DCQ24336900-D9DE2889-FC63-4832-AC13-8CCA8629B14D
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Chromodomain helicase DNA binding protein 7
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
CHD7
@ru
Chromodomain helicase DNA binding protein 7
@en
Chromodomain helicase DNA binding protein 7
@nl
type
label
CHD7
@ru
Chromodomain helicase DNA binding protein 7
@en
Chromodomain helicase DNA binding protein 7
@nl
altLabel
ATP-dependent helicase CHD7
@en
CHARGE association
@en
CHD7
@en
chromodomain helicase DNA binding protein 7 isoform CRA_e
@en
chromodomain-helicase-DNA-binding protein 7
@en
prefLabel
CHD7
@ru
Chromodomain helicase DNA binding protein 7
@en
Chromodomain helicase DNA binding protein 7
@nl
P361
P527
P637
P638
P680
P681
P682
P705
P352
P2888
P31
P352
P361
P527
P637
NP_001303619
XP_011515855
XP_011515856
XP_011515857
XP_011515862
XP_016869101
XP_016869102
P638
P680
P682
P702
P703
P705
ENSP00000392028
ENSP00000432627
ENSP00000433336
ENSP00000436027
ENSP00000436492
ENSP00000437061