Entity Details

Primary name TPC14_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8WVR3
EntryNameTPC14_HUMAN
FullNameTrafficking protein particle complex subunit 14
TaxID9606
Evidenceevidence at protein level
Length580
SequenceStatuscomplete
DateCreated2007-03-20
DateModified2021-06-02

Ontological Relatives

GenesTRAPPC14

GO terms

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GOName
GO:0005886 plasma membrane
GO:0030496 midbody
GO:0034451 centriolar satellite
GO:0042127 regulation of cell population proliferation
GO:0043014 alpha-tubulin binding
GO:0043231 intracellular membrane-bounded organelle
GO:0060271 cilium assembly
GO:0072686 mitotic spindle
GO:1990071 TRAPPII protein complex

Subcellular Location

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Subcellular Location
Cytoplasm
Midbody
Vesicle

Domains

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DomainNameCategoryType
IPR031626 Trafficking protein particle complex subunit 14FamilyFamily

Diseases

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Disease IDSourceNameDescription
618351 OMIMMicrocephaly 25, primary, autosomal recessive (MCPH25)A form of microcephaly, a disease defined as a head circumference more than 3 standard deviations below the age, sex and ethnically matched mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. MCPH25 patients additionally manifest global developmental delay, severe intellectual disability with speech impairment, attention deficit-hyperactivity disorder, and reduced white matter and thin corpus callosum on brain imaging. The disease is caused by variants affecting the gene represented in this entry.