MSL3, MSL complex subunit 3, 10943

N. diseases: 32; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR The MSL complex: juggling RNA-protein interactions for dosage compensation and beyond. 25900149 2015
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR The MSL complex: juggling RNA-protein interactions for dosage compensation and beyond. 25900149 2015
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Mof-associated complexes have overlapping and unique roles in regulating pluripotency in embryonic stem cells and during differentiation. 24898753 2014
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Mof-associated complexes have overlapping and unique roles in regulating pluripotency in embryonic stem cells and during differentiation. 24898753 2014
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Structural and biochemical studies on the chromo-barrel domain of male specific lethal 3 (MSL3) reveal a binding preference for mono- or dimethyllysine 20 on histone H4. 20943666 2010
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Corecognition of DNA and a methylated histone tail by the MSL3 chromodomain. 20657587 2010
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Structural and biochemical studies on the chromo-barrel domain of male specific lethal 3 (MSL3) reveal a binding preference for mono- or dimethyllysine 20 on histone H4. 20943666 2010
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Corecognition of DNA and a methylated histone tail by the MSL3 chromodomain. 20657587 2010
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16. 16227571 2005
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16. 16227571 2005
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR The MRG domain mediates the functional integration of MSL3 into the dosage compensation complex. 15988010 2005
dbSNP: rs1555907215
rs1555907215
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR The MRG domain mediates the functional integration of MSL3 into the dosage compensation complex. 15988010 2005
dbSNP: rs1555906707
rs1555906707
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555906768
rs1555906768
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555906781
rs1555906781
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555907620
rs1555907620
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555907623
rs1555907623
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555907626
rs1555907626
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555907653
rs1555907653
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
GC 0.700 GeneticVariation CLINVAR
dbSNP: rs1555907864
rs1555907864
Entrez Id: 10943
Gene Symbol: MSL3
MSL3
CUI: C1843367
Disease:
Poor school performance
A 0.700 GeneticVariation CLINVAR