Entity Details

Primary name MS3L1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N5Y2
EntryNameMS3L1_HUMAN
FullNameMale-specific lethal 3 homolog
TaxID9606
Evidenceevidence at protein level
Length521
SequenceStatuscomplete
DateCreated2003-06-20
DateModified2021-06-02

Ontological Relatives

GenesMSL3

GO terms

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GOName
GO:0000123 histone acetyltransferase complex
GO:0003677 DNA binding
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0006342 chromatin silencing
GO:0006355 regulation of transcription, DNA-templated
GO:0016573 histone acetylation
GO:0016575 histone deacetylation
GO:0035064 methylated histone binding
GO:0035267 NuA4 histone acetyltransferase complex
GO:0043967 histone H4 acetylation
GO:0043968 histone H2A acetylation
GO:0043984 histone H4-K16 acetylation
GO:0046972 histone acetyltransferase activity (H4-K16 specific)
GO:0072487 MSL complex

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR000953 Chromo/chromo shadow domainDomainDomain
IPR008676 MRGFamilyFamily
IPR016197 Chromo-like domain superfamilyFamilyHomologous superfamily
IPR025995 RNA binding activity-knot of a chromodomainDomainDomain
IPR026541 MRG domainDomainDomain
IPR037921 Male-specific lethal 3 homologFamilyFamily
IPR038217 MRG, C-terminal domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
301032 OMIMBasilicata-Akhtar syndrome (MRXSBA)A mental retardation syndrome characterized by global developmental delay, progressive gait disturbance, poor or absent speech, facial dysmorphism, and mild distal skeletal anomalies. Mental retardation is defined by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry.