Entity Details

Primary name KLD8B_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8IXV7
EntryNameKLD8B_HUMAN
FullNameKelch domain-containing protein 8B
TaxID9606
Evidenceevidence at transcript level
Length354
SequenceStatuscomplete
DateCreated2005-12-20
DateModified2021-06-02

Ontological Relatives

GenesKLHDC8B

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0030496 midbody
GO:0045171 intercellular bridge
GO:0098813 nuclear chromosome segregation
GO:0110070 cellularization cleavage furrow
GO:0140014 mitotic nuclear division
GO:1902410 mitotic cytokinetic process

Subcellular Location

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Subcellular Location
Cytoplasm
Midbody

Domains

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DomainNameCategoryType
IPR006652 Kelch repeat type 1RepeatRepeat
IPR015915 Kelch-type beta propellerFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
236000 OMIMLymphoma, Hodgkin, classic (CHL)A malignant disease characterized by progressive enlargement of the lymph nodes, spleen and general lymphoid tissue, and the presence of large, usually multinucleate, cells (Reed-Sternberg cells). Reed-Sternberg cells compose only 1-2% of the total tumor cell mass. The remainder is composed of a variety of reactive, mixed inflammatory cells consisting of lymphocytes, plasma cells, neutrophils, eosinophils and histiocytes. Disease susceptibility is associated with variants affecting the gene represented in this entry. A variant in the 5'-UTR of KLHDC8B, responsible for decreasing its expression, is associated with classic Hodgkin lymphoma and segregates with the disease in some families (PubMed:19706467).

Interactions

0 interactions

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