Entity Details

Primary name CCNK_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO75909
EntryNameCCNK_HUMAN
FullNameCyclin-K
TaxID9606
Evidenceevidence at protein level
Length580
SequenceStatuscomplete
DateCreated2000-12-01
DateModified2021-06-02

Ontological Relatives

GenesCCNK

GO terms

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GOName
GO:0000079 regulation of cyclin-dependent protein serine/threonine kinase activity
GO:0002944 cyclin K-CDK12 complex
GO:0002945 cyclin K-CDK13 complex
GO:0004693 cyclin-dependent protein serine/threonine kinase activity
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0006357 regulation of transcription by RNA polymerase II
GO:0006366 transcription by RNA polymerase II
GO:0006368 transcription elongation from RNA polymerase II promoter
GO:0006974 cellular response to DNA damage stimulus
GO:0007049 cell cycle
GO:0008024 cyclin/CDK positive transcription elongation factor complex
GO:0008353 RNA polymerase II CTD heptapeptide repeat kinase activity
GO:0016538 cyclin-dependent protein serine/threonine kinase regulator activity
GO:0019901 protein kinase binding
GO:0032786 positive regulation of DNA-templated transcription, elongation
GO:0042795 snRNA transcription by RNA polymerase II
GO:0044828 negative regulation by host of viral genome replication
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0051301 cell division
GO:0061575 cyclin-dependent protein serine/threonine kinase activator activity
GO:2001165 positive regulation of phosphorylation of RNA polymerase II C-terminal domain serine 2 residues

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR004367 Cyclin, C-terminal domainDomainDomain
IPR006671 Cyclin, N-terminalDomainDomain
IPR013763 Cyclin-likeDomainDomain
IPR036915 Cyclin-like superfamilyFamilyHomologous superfamily
IPR043198 Cyclin/Cyclin-like subunit Ssn8FamilyFamily

Diseases

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Disease IDSourceNameDescription
618147 OMIMIntellectual developmental disorder with hypertelorism and distinctive facies (IDDHDF)An autosomal dominant neurodevelopmental disorder characterized by developmental delay and intellectual disability, language defects, and distinctive facial dysmorphism including high hairline, hypertelorism, thin eyebrows, dysmorphic ears, broad nasal bridge and tip, and narrow jaw. The disease is caused by variants affecting the gene represented in this entry.

Interactions

57 interactions

InteractorPartnerSourcesPublicationsLink
CCNK_HUMANDVL3_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANT22D4_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANCC85B_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANUSBP1_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANFBLN4_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANKCNRG_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANFKBP6_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANSTX11_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANRFX6_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANRBPMS_HUMANBioGRID, HPRD, IntAct16189514 25416956 details
CCNK_HUMANCEP76_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANRHXF2_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANKR412_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANCDK18_HUMANBioGRID, HPRD, IntAct16189514 32296183 details
CCNK_HUMANHM20A_HUMANBioGRID, HPRD, IntAct16189514 details
CCNK_HUMANATX1_HUMANBioGRID, HPRD, IntAct16713569 32814053 details
CCNK_HUMANBHE40_HUMANBioGRID, IntAct25416956 details
CCNK_HUMANNDC80_HUMANBioGRID, IntAct25416956 details
CCNK_HUMANTLE5_HUMANBioGRID, IntAct25416956 32296183 details
CCNK_HUMANLZTS2_HUMANBioGRID, IntAct25416956 details
CCNK_HUMANCDK13_HUMANBioGRID, IntAct26186194 26748711 28514442 details
CCNK_HUMANPIN1_HUMANBioGRID, IntAct16055720 26748711 details
CCNK_HUMANCDK16_HUMANIntAct22184064 details
CCNK_HUMANPR20D_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANUBP54_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANCRTP1_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANDDT4L_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANKR196_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANHXA1_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANKR132_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANMYCL_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANKR197_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANRUNX1_HUMANBioGRID, IntAct28533407 32296183 details
CCNK_HUMANZN446_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANHSFY1_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANPO6F2_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANOXER1_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANHNRH2_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANKRA62_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANF168B_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANRPAC1_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANHNRH1_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANKRA81_HUMANBioGRID, IntAct32296183 details
CCNK_HUMANNECA2_HUMANBioGRID, HPRD16189514 details
CCNK_HUMANCDK9_HUMANBioGRID, HPRD10574912 11884399 details
CCNK_HUMANZEP1_HUMANBioGRID32296183 details
CCNK_HUMANPR20E_HUMANBioGRID32296183 details
CCNK_HUMANPR20C_HUMANBioGRID32296183 details
CCNK_HUMANPR20B_HUMANBioGRID32296183 details
CCNK_HUMANPR20A_HUMANBioGRID32296183 details
CCNK_HUMANHOMEZ_HUMANBioGRID32296183 details
CCNK_HUMANDDB1_HUMANBioGRID32494016 32804079 details
CCNK_HUMANRBX1_HUMANBioGRID32804079 details
CCNK_HUMANCDK2_HUMANHPRD10574912 9632813 details
CCNK_HUMANRPB1_HUMANBioGRID, DIP, HPRD, IntAct26659056 26748711 9632813 details
CCNK_HUMANCDK12_HUMANBioGRID, DIP, IntAct22939629 26344197 26659056 26748711 32804079 details
CCNK_HUMANSET1A_HUMANBioGRID29474905 details