Entity Details

Primary name MPLKI_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8TAP9
EntryNameMPLKI_HUMAN
FullNameM-phase-specific PLK1-interacting protein
TaxID9606
Evidenceevidence at protein level
Length179
SequenceStatuscomplete
DateCreated2005-07-19
DateModified2021-06-02

Ontological Relatives

GenesMPLKIP

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005813 centrosome
GO:0007049 cell cycle
GO:0030496 midbody
GO:0043231 intracellular membrane-bounded organelle
GO:0051301 cell division

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR026618 M-phase-specific PLK1-interacting protein-like, vertebrateFamilyFamily
IPR028265 TTDN1/Protein SICKLEFamilyFamily

Diseases

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Disease IDSourceNameDescription
234050 OMIMTrichothiodystrophy 4, non-photosensitive (TTD4)A form of trichothiodystrophy, an autosomal recessive disease characterized by sulfur-deficient brittle hair and multisystem variable abnormalities. The spectrum of clinical features varies from mild disease with only hair involvement to severe disease with cutaneous, neurologic and profound developmental defects. Ichthyosis, intellectual and developmental disabilities, decreased fertility, abnormal characteristics at birth, ocular abnormalities, short stature, and infections are common manifestations. There are both photosensitive and non-photosensitive forms of the disorder. TTD4 patients do not manifest cutaneous photosensitivity. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
MPLKI_HUMANAKP8L_HUMANIntAct32296183 details
MPLKI_HUMANGORS2_HUMANBioGRID, IntAct32296183 details
MPLKI_HUMANNTAQ1_HUMANBioGRID, IntAct32296183 details