Entity Details

Primary name STIL_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ15468
EntryNameSTIL_HUMAN
FullNameSCL-interrupting locus protein
TaxID9606
Evidenceevidence at protein level
Length1287
SequenceStatuscomplete
DateCreated2007-01-09
DateModified2021-06-02

Ontological Relatives

GenesSTIL

GO terms

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GOName
GO:0000578 embryonic axis specification
GO:0001701 in utero embryonic development
GO:0001843 neural tube closure
GO:0001947 heart looping
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005814 centriole
GO:0005829 cytosol
GO:0007052 mitotic spindle organization
GO:0007224 smoothened signaling pathway
GO:0007368 determination of left/right symmetry
GO:0021915 neural tube development
GO:0030900 forebrain development
GO:0030903 notochord development
GO:0033504 floor plate development
GO:0035264 multicellular organism growth
GO:0042802 identical protein binding
GO:0043066 negative regulation of apoptotic process
GO:0046599 regulation of centriole replication
GO:0051298 centrosome duplication
GO:0071539 protein localization to centrosome

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR026123 SCL-interrupting locus proteinFamilyFamily

Diseases

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Disease IDSourceNameDescription
612703 OMIMMicrocephaly 7, primary, autosomal recessive (MCPH7)A disease defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Affected individuals are mentally retarded. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits due to degenerative brain disorder. The disease is caused by variants affecting the gene represented in this entry.