Entity Details

Primary name KLH15_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96M94
EntryNameKLH15_HUMAN
FullNameKelch-like protein 15
TaxID9606
Evidenceevidence at protein level
Length604
SequenceStatuscomplete
DateCreated2006-02-21
DateModified2021-06-02

Ontological Relatives

GenesKLHL15

GO terms

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GOName
GO:0005634 nucleus
GO:0006511 ubiquitin-dependent protein catabolic process
GO:0016567 protein ubiquitination
GO:0031463 Cul3-RING ubiquitin ligase complex
GO:0071630 nuclear protein quality control by the ubiquitin-proteasome system
GO:2000042 negative regulation of double-strand break repair via homologous recombination

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR000210 BTB/POZ domainDomainDomain
IPR006652 Kelch repeat type 1RepeatRepeat
IPR011333 SKP1/BTB/POZ domain superfamilyFamilyHomologous superfamily
IPR011705 BTB/Kelch-associatedDomainDomain
IPR015915 Kelch-type beta propellerFamilyHomologous superfamily
IPR017096 BTB-kelch proteinFamilyFamily
IPR030597 Kelch-like protein 15FamilyFamily

Diseases

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Disease IDSourceNameDescription
300982 OMIMMental retardation, X-linked 103 (MRX103)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. The disease may be caused by variants affecting the gene represented in this entry.