Entity Details

Primary name RTTN_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ86VV8
EntryNameRTTN_HUMAN
FullNameRotatin
TaxID9606
Evidenceevidence at protein level
Length2226
SequenceStatuscomplete
DateCreated2007-10-23
DateModified2021-06-02

Ontological Relatives

GenesRTTN

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005814 centriole
GO:0007099 centriole replication
GO:0007368 determination of left/right symmetry
GO:0010457 centriole-centriole cohesion
GO:0032053 ciliary basal body organization
GO:0036064 ciliary basal body

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR011989 Armadillo-like helicalFamilyHomologous superfamily
IPR016024 Armadillo-type foldFamilyHomologous superfamily
IPR029249 Rotatin, N-terminalDomainDomain
IPR030791 RotatinFamilyFamily

Diseases

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Disease IDSourceNameDescription
614833 OMIMMicrocephaly, short stature, and polymicrogyria with or without seizures (MSSP)A disease characterized by many irregular small gyri in the brain surface and fusion of the molecular layer over multiple small gyri, which gives a festooned appearance to the cortical surface, without abnormal neuronal migration. Polymicrogyria is a heterogeneous disorder, considered to be the result of postmigratory abnormal cortical organization. MSSP patients have moderate to severe mental retardation, poor speech, dysarthria and seizures. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions