CCNH - cyclin H Gene

Also Known as CAK; p34; p37; CycH

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 902

About CCNH

Cytogenetic location: 5q14.3 Genomic coordinates (GRCh38): 5:87,311,471-87,412,930 (from NCBI)

This gene has 13 transcripts (splice variants), 216 orthologues and 6 paralogues. Ubiquitous expression in placenta (RPKM 15.0), testis (RPKM 11.2) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with CDK7 kinase and ring finger protein MAT1. The kinase complex is able to phosphorylate CDK2 and CDC2 kinases, thus functions as a CDK-activating kinase (CAK). This cyclin and its kinase partner are components of TFIIH, as well as RNA polymerase II protein complexes. They participate in two different transcriptional regulation processes, suggesting an important link between basal transcription control and the cell cycle machinery. A pseudogene of this gene is found on chromosome 4. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Nov 2010]

CCNH Products (5)

mRNA Protein Name
NM_001199189.2 NP_001186118.1 cyclin-H isoform 2
NM_001239.4 NP_001230.1 cyclin-H isoform 1
NM_001363539.2 NP_001350468.1 cyclin-H isoform 3
NM_001364075.2 NP_001351004.1 cyclin-H isoform 4
NM_001364076.2 NP_001351005.1 cyclin-H isoform 5
Molecular Function GO Annotation Evidence References Source
contributes to RNA polymerase II general transcription initiation factor activity IDA
IDA: Inferred from direct assay
7533895 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8521818 GOA
Biological Process GO Annotation Evidence References Source
involved in protein stabilization IMP
IMP: Inferred from mutant phenotype
23393140 GOA
involved in regulation of G1/S transition of mitotic cell cycle IDA
IDA: Inferred from direct assay
23622515 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9852112 GOA
involved in transcription initiation at RNA polymerase II promoter IDA
IDA: Inferred from direct assay
7533895 GOA
Cellular Component GO Annotation Evidence References Source
part of CAK-ERCC2 complex IDA
IDA: Inferred from direct assay
8692841 GOA
part of cyclin-dependent protein kinase holoenzyme complex IDA
IDA: Inferred from direct assay
23622515 GOA
part of transcription factor TFIIH core complex IDA
IDA: Inferred from direct assay
8692841 GOA
part of transcription factor TFIIH holo complex IDA
IDA: Inferred from direct assay
9852112 GOA
part of transcription factor TFIIK complex IDA
IDA: Inferred from direct assay
8692841 GOA
part of transcription factor TFIIK complex IMP
IMP: Inferred from mutant phenotype
23393140 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CCNH Protein Structure

Cyclin_N

Cyclin_N: Cyclin, N-terminal domain (74 - 158)

  • 0
  • 100
  • 200
  • 300
  • 323 a.a.
Protein Preferred Names Protein Names

cyclin-H

  • CAK complex subunit

CCNH Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CCNH P51946 MTMR7 Homo sapiens Q9Y216 32296183
Intra
CCNH P51946 TRIML2 Homo sapiens Q8N7C3 32296183
Intra
CCNH P51946 TCF12 Homo sapiens Q99081-3 32296183
Intra
CCNH P51946 TCF12 Homo sapiens Q99081-3 32296183
Intra
CCNH P51946 TCF12 Homo sapiens Q99081-3 32296183
Intra
CCNH P51946 RHOH Homo sapiens Q15669 32296183
Intra
CCNH P51946 RHOH Homo sapiens Q15669 32296183
Intra
CCNH P51946 RHOH Homo sapiens Q15669 32296183
Intra
CCNH P51946 CDK3 Homo sapiens Q00526 32296183
Intra
CCNH P51946 TCF4 Homo sapiens P15884-3 32296183
Intra
CCNH P51946 TCF4 Homo sapiens P15884-3 32296183
Intra
CCNH P51946 KLC3 Homo sapiens Q6P597 25416956
Intra
CCNH P51946 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
CCNH P51946 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
CCNH P51946 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
CCNH P51946 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
CCNH P51946 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
CCNH P51946 CCDC170 Homo sapiens Q8IYT3 25416956
Intra
CCNH P51946 CCDC170 Homo sapiens Q8IYT3 25416956
Intra
CCNH P51946 CDK6 Homo sapiens Q00534 32296183
Intra
CCNH P51946 SNAPIN Homo sapiens O95295 32296183
Intra
CCNH P51946 SNAPIN Homo sapiens O95295 32296183
Intra
CCNH P51946 MCRS1 Homo sapiens Q96EZ8 32296183
Intra
CCNH P51946 MCRS1 Homo sapiens Q96EZ8 32296183
Intra
CCNH P51946 MCRS1 Homo sapiens Q96EZ8 32296183
Intra
CCNH P51946 CCT4 Homo sapiens P50991 32296183
Intra
CCNH P51946 CCT4 Homo sapiens P50991 32296183
Intra
CCNH P51946 PSMA1 Homo sapiens P25786 25416956
Intra
CCNH P51946 PSMA1 Homo sapiens P25786 25416956
Intra
CCNH P51946 PSMA1 Homo sapiens P25786 16189514
Intra
CCNH P51946 RARA Homo sapiens P10276 16769902
Intra
CCNH P51946 RARA Homo sapiens P10276 16769902
Intra
CCNH P51946 SFN Homo sapiens P31947 25416956
Intra
CCNH P51946 GOLGA2 Homo sapiens Q08379 32296183
Intra
CCNH P51946 GOLGA2 Homo sapiens Q08379 25416956
Intra
CCNH P51946 GOLGA2 Homo sapiens Q08379 32296183
Intra
CCNH P51946 GOLGA2 Homo sapiens Q08379
Y2H
21988832
Intra
CCNH P51946 GOLGA2 Homo sapiens Q08379 25416956
Intra
CCNH P51946 GOLGA2 Homo sapiens Q08379 32296183
Intra
CCNH P51946 ZNF655 Homo sapiens Q8N720 32296183
Intra
CCNH P51946 ZNF655 Homo sapiens Q8N720 32296183
Intra
CCNH P51946 ZNF655 Homo sapiens Q8N720 32296183
Intra
CCNH P51946 DUSP12 Homo sapiens Q9UNI6 32296183
Intra
CCNH P51946 DUSP12 Homo sapiens Q9UNI6 25416956
Intra
CCNH P51946 DUSP12 Homo sapiens Q9UNI6 32296183
Intra
CCNH P51946 DUSP12 Homo sapiens Q9UNI6 25416956
Intra
CCNH P51946 DUSP12 Homo sapiens Q9UNI6 32296183
Intra
CCNH P51946 GRIPAP1 Homo sapiens Q4V328 32296183
Intra
CCNH P51946 GRIPAP1 Homo sapiens Q4V328 32296183
Intra
CCNH P51946 GRIPAP1 Homo sapiens Q4V328 32296183
Intra
CCNH P51946 CALCOCO2 Homo sapiens Q13137 25416956
Intra
CCNH P51946 CALCOCO2 Homo sapiens Q13137 25416956
Intra
CCNH P51946 SORBS3 Homo sapiens O60504 32296183
Intra
CCNH P51946 SORBS3 Homo sapiens O60504 32296183
Intra
CCNH P51946 ZNRD2 Homo sapiens O60232 16189514
Intra
CCNH P51946 ZNRD2 Homo sapiens O60232 25416956
Intra
CCNH P51946 CTBP2 Homo sapiens P56545 21988832
Intra
CCNH P51946 CTBP2 Homo sapiens P56545
Y2H
21988832
Intra
CCNH P51946 CTBP2 Homo sapiens P56545 21988832
Intra
CCNH P51946 DDIT4L Homo sapiens Q96D03 32296183
Intra
CCNH P51946 DDIT4L Homo sapiens Q96D03 32296183
Intra
CCNH P51946 DDIT4L Homo sapiens Q96D03 32296183
Intra
CCNH P51946 PPFIA1 Homo sapiens Q13136 25416956
Intra
CCNH P51946 PPFIA1 Homo sapiens Q13136 25416956
Intra
CCNH P51946 PPFIA1 Homo sapiens Q13136 29892012
Intra
CCNH P51946 PICK1 Homo sapiens Q9NRD5 32296183
Intra
CCNH P51946 PICK1 Homo sapiens Q9NRD5 32296183
Intra
CCNH P51946 PICK1 Homo sapiens Q9NRD5 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CCNH Proteins

Cat. No. Product Name Accession Purity
HY-P75361 CDK7-CCNH-MNAT1 Protein, Human (Active, sf9, His) P50613 (A2-F346)&P51946 (Y2-L323)&P51948 (D2-S309) ≥ 85%, as determined by reducing SDS-PAGE.

CCNH Antibodies

Cat. No. Product Name Application Reactivity
HY-P80636 Cyclin H Antibody (YA788) WB Human, Mouse
HY-P80636A Cyclin H Antibody (YA788)(PBS only) WB Human, Mouse
HY-P80637 Cyclin H Antibody (YA482) WB, IHC-P, ICC/IF, IP, FC, IF-Tissue Human, Mouse
HY-P85424 Cyclin H Antibody (YA5116) WB Human, Mouse, Rat, Dog, Pig
HY-P85532 Cyclin H Antibody (YA5224) WB, IP Human
HY-P85532A Cyclin H Antibody (YA5224)(PBS only) WB, IP Human

Related Diseases

Diseases Alias
Basal Cell Carcinoma, Multiple
  • Multiple Basal Cell Carcinoma

Angioosteohypertrophic Syndrome
  • Klippel-Trenaunay-Weber Syndrome

  • Haemangiectatic Hypertrophy

Capillary Malformation-Arteriovenous Malformation 1
  • Parkes Weber Syndrome

  • Capillary Malformation-Arteriovenous Malformation

  • Capillary Malformation-Arteriovenous Malformation Syndrome

  • CMAVM1

  • Cmavm

  • Cm-Avm Syndrome

  • Pkws

  • Cm-Avm

  • Parkes-Weber Syndrome

  • Capillary Malformation-Arteriovenous Malformation, Type 1

Basal Cell Carcinoma 1
  • Basal Cell Carcinoma, Susceptibility To, 1

  • Basal Cell Carcinoma

  • BCC1

  • BCC

  • Multiple Basal Cell Carcinoma

  • Non-Syndromic Basal Cell Carcinoma

  • Carcinoma, Basal Cell, Susceptibility To, Type 1

  • Experimental Organism Basal Cell Carcinoma

  • Basal Cell Carcinoma, Multiple

Telangiectasia, Hereditary Hemorrhagic, Type 1
  • Orw Disease

  • HHT1

  • Hht

  • Telangiectasia, Hereditary Hemorrhagic, Of Rendu, Osler, And Weber

  • Osler-Rendu-Weber Disease

  • Telangiectasia, Hereditary Hemorrhagic, 1

  • Hereditary Hemorrhagic Telangiectasia Of Rendu, Osler, And Weber

  • Orw1

  • Osler-Rendu-Weber Syndrome

  • Osler-Rendu-Weber Syndrome 1

  • Telangiectasia Hemorrhagic, Hereditary, Type 1

  • Hereditary Hemorrhagic Telangiectasia

Hemangioma, Capillary Infantile
  • HCI

  • Capillary Infantile Hemangioma

  • Hemangioma, Hereditary Capillary

  • Hemangioma, Capillary Infantile, Susceptibility To

  • Hemangioma, Capillary Infantile, Somatic

  • Hemangioma Hereditary Capillary

Hereditary Hemorrhagic Telangiectasia
  • Rendu-Osler-Weber Disease

  • Hht

  • Osler-Weber-Rendu Disease

  • Telangiectasia, Hereditary Hemorrhagic

  • Osler Hemorrhagic Telangiectasia Syndrome

  • Orw Disease

  • Osler Weber Rendu Syndrome

  • Osler-Rendu-Weber Disease

  • Osler-Weber-Rendu Syndrome

  • Rendu-Osler Disease

  • Telangiectasia Hereditary Hemorrhagic

  • Telangiectasia Hemorrhagic, Hereditary

  • Hht - [Hereditary Haemorrhagic Telangiectasia]

  • Osler Haemorrhagic Telangiectasia Syndrome

Klippel-Trenaunay-Weber Syndrome
  • Klippel-Trenaunay Syndrome

  • KTS

  • Ktw Syndrome

  • Angioosteohypertrophy Syndrome

  • Angio-Osteohypertrophy Syndrome

  • Klippel Trenaunay Syndrome

  • Klippel-Trénaunay-Weber Syndrome

  • Haemangiectatic Hypertrophy

  • Weber-Klippel-Trenaunay

  • Congenital Dysplastic Angiopathy

  • Klippel-Trenaunay Disease

  • Weber Klippel Trenaunay

Trichothiodystrophy
  • Ttd

  • Amish Brittle Hair Syndrome

  • Bids Syndrome

  • Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome

  • Ibids

  • Pibids

  • Trichothiodystrophy Syndromes

Cockayne Syndrome
  • Cockayne'S Syndrome

  • Dwarfism-Retinal Atrophy-Deafness Syndrome

  • Neill-Dingwall Syndrome

  • Progeria-Like Syndrome

  • Progeroid Nanism

  • Cs

Xeroderma Pigmentosum, Complementation Group B
  • Xeroderma Pigmentosum Group B

  • Xeroderma Pigmentosum, Group B

  • XPB

  • Xpbc

  • Xp Group B

  • Xp, Group B

  • Xeroderma Pigmentosum Complementation Group B

  • XP-B

  • Xeroderma Pigmentosum Group B With Cockayne Syndrome

  • Xeroderma Pigmentosum Ii

  • Xp2

  • Xp-B/Cs

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Xeroderma Pigmentosum, Complementation Group D
  • Xeroderma Pigmentosum, Group D

  • Xpdc

  • Xeroderma Pigmentosum Iv

  • XPD

  • Xeroderma Pigmentosum Group D

  • Xeroderma Pigmentosum Viii

  • Xp Group D

  • Xp Group H

  • Xp4

  • Xp8

  • Xph

  • Xp, Group D

  • Xp4 Xeroderma Pigmentosum Viii, Formerly

  • Xp8, Formerly

  • Xp, Group H, Formerly

  • Xph, Formerly

  • Xeroderma Pigmentosum Complementation Group D

  • XP-D

  • Xp-D/Cs

Xeroderma Pigmentosum, Variant Type
  • Xeroderma Pigmentosum

  • XPV

  • Xeroderma Pigmentosum Variant Type

  • Xeroderma Pigmentosum With Normal Dna Repair Rates

  • Photosensitivity With Defective Dna Synthesis

  • Xp

  • De Sanctis-Cacchione Syndrome

  • Desanctis-Cacchione Syndrome

  • Xeroderma Pigmentosa

  • Xerodermic Idiocy

  • Xeroderma Pigmentosum Variant

  • Xp - [Xeroderma Pigmentosum]

  • Atrophoderma Pigmentosum

Xeroderma Pigmentosum, Complementation Group G
  • Xeroderma Pigmentosum, Group G

  • Xeroderma Pigmentosum Vii

  • Xp7

  • XPG

  • Xeroderma Pigmentosum Group G

  • Xp Group G

  • Xp, Group G

  • Xpgc

  • Xeroderma Pigmentosum, Group G/Cockayne Syndrome

  • Xeroderma Pigmentosum, Type 7

  • Xeroderma Pigmentosum Complementation Group G

  • XP-G

  • Xp-G/Cs

  • Xeroderma Pigmentosum Group G/Cockayne Syndrome

Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations
  • Star Syndrome

  • Syndactyly-Telecanthus-Anogenital And Renal Malformations Syndrome

  • Syndactyly With Renal And Anogenital Malformations

  • STAR

  • Syndactyly, Telecanthus, Anogenital And Renal Malformations

  • Toe Syndactyly, Telecanthus, Anogenital And Renal Malformations

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus CCNH VGNC VGNC:60561
Mus musculus CCNH MGD MGI:1913921
Canis familiaris CCNH VGNC VGNC:38902
Macaca mulatta CCNH VGNC VGNC:70732
Rattus norvegicus CCNH RGD RGD:69419
Bos taurus CCNH VGNC VGNC:97249
Others CCNH NCBI