Entity Details

Primary name KBP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96EK5
EntryNameKBP_HUMAN
FullNameKIF-binding protein
TaxID9606
Evidenceevidence at protein level
Length621
SequenceStatuscomplete
DateCreated2005-08-30
DateModified2021-06-02

Ontological Relatives

GenesKIFBP

GO terms

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GOName
GO:0005739 mitochondrion
GO:0005856 cytoskeleton
GO:0006839 mitochondrial transport
GO:0007399 nervous system development
GO:0019894 kinesin binding
GO:0030154 cell differentiation

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR011990 Tetratricopeptide-like helical domain superfamilyFamilyHomologous superfamily
IPR022083 KIF-1 binding proteinFamilyFamily

Diseases

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Disease IDSourceNameDescription
609460 OMIMGoldberg-Shprintzen syndrome (GOSHS)A disorder characterized by intellectual disability, microcephaly, and dysmorphic facial features. Most patients also have Hirschsprung disease. The disease is caused by variants affecting the gene represented in this entry.