CUL4A - cullin 4A Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8451

About CUL4A

Cytogenetic location: 13q34 Genomic coordinates (GRCh38): 13:113,208,193-113,267,108 (from NCBI)

This gene has 12 transcripts (splice variants), 206 orthologues and 7 paralogues. Ubiquitous expression in testis (RPKM 20.5), heart (RPKM 17.9) and 25 other tissues.

Summary

CUL4A is the ubiquitin Ligase component of a multimeric complex involved in the degradation of DNA damage-response proteins (Liu et al., 2009 [PubMed 19481525]).[supplied by OMIM, Oct 2009]

CUL4A Products (11)

mRNA Protein Name
NM_001008895.4 NP_001008895.1 cullin-4A isoform 1
NM_001278513.3 NP_001265442.1 cullin-4A isoform 2
NM_001278514.3 NP_001265443.1 cullin-4A isoform 3
NM_001354938.2 NP_001341867.1 cullin-4A isoform 2
NM_001354939.2 NP_001341868.1 cullin-4A isoform 2
NM_001354940.2 NP_001341869.1 cullin-4A isoform 2
NM_001354941.2 NP_001341870.1 cullin-4A isoform 4
NM_001354942.2 NP_001341871.1 cullin-4A isoform 4
NM_001354943.2 NP_001341872.1 cullin-4A isoform 5
NM_001354944.2 NP_001341873.1 cullin-4A isoform 6
NM_003589.4 NP_003580.1 cullin-4A isoform 2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
12504025 GOA
enables ubiquitin ligase complex scaffold activity IDA
IDA: Inferred from direct assay
34065512 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
20870715 GOA
enables ubiquitin protein ligase binding IDA
IDA: Inferred from direct assay
11027288 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA damage response EXP
EXP: Inferred from Experiment
22118460 GOA
involved in T cell activation IDA
IDA: Inferred from direct assay
34065512 GOA
involved in cellular response to UV EXP
EXP: Inferred from Experiment
22118460 GOA
involved in positive regulation of protein catabolic process IDA
IDA: Inferred from direct assay
11027288 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
14739464 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
26431207 GOA
involved in protein ubiquitination IMP
IMP: Inferred from mutant phenotype
28437394 GOA
involved in ribosome biogenesis IMP
IMP: Inferred from mutant phenotype
26711351 GOA
involved in spermatogenesis IDA
IDA: Inferred from direct assay
34065512 GOA
involved in ubiquitin-dependent protein catabolic process via the C-end degron rule pathway IDA
IDA: Inferred from direct assay
34065512 GOA
Cellular Component GO Annotation Evidence References Source
part of Cul4-RING E3 ubiquitin ligase complex IDA
IDA: Inferred from direct assay
16949367 GOA
part of Cul4A-RING E3 ubiquitin ligase complex EXP
EXP: Inferred from Experiment
22118460 GOA
part of Cul4A-RING E3 ubiquitin ligase complex IDA
IDA: Inferred from direct assay
12732143 GOA
is active in cytoplasm IDA
IDA: Inferred from direct assay
34065512 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
10585395 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

CUL4A Protein Structure

Cullin

Cullin: Cullin family (63 - 661)

Cullin_Nedd8

Cullin_Nedd8: Cullin protein neddylation domain (689 - 753)

  • 0
  • 200
  • 400
  • 600
  • 759 a.a.
Protein Preferred Names Protein Names

cullin-4A

  • CUL-4A

CUL4A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CUL4A Q13619 DDB2 Homo sapiens Q92466 17041588
Intra
CUL4A Q13619 DDB2 Homo sapiens Q92466 30945288
Intra
CUL4A Q13619 DDB2 Homo sapiens Q92466
TAP
21145461
Intra
CUL4A Q13619 UBXN7 Homo sapiens O94888 22466964
Intra
CUL4A Q13619 DDB1 Homo sapiens Q16531 30945288
Intra
CUL4A Q13619 DDB1 Homo sapiens Q16531
TAP
21145461
Intra
CUL4A Q13619 DDB1 Homo sapiens Q16531 17041588
Intra
CUL4A Q13619 DDB1 Homo sapiens Q16531 22157821
Intra
CUL4A Q13619 HSP90AB1 Homo sapiens P08238 22939624
Intra
CUL4A Q13619 HSP90AB1 Homo sapiens P08238
TAP
21145461
Intra
CUL4A Q13619 VCP Homo sapiens P55072 22466964
Intra
CUL4A Q13619 CAND1 Homo sapiens Q86VP6 12609982
Intra
CUL4A Q13619 CAND1 Homo sapiens Q86VP6 12504026
Intra
CUL4A Q13619 CAND1 Homo sapiens Q86VP6
TAP
21145461
Cross: Cross-species interaction Intra: Intraspecies interaction

CUL4A Antibodies

Cat. No. Product Name Application Reactivity
HY-P86842 Cullin 4a Antibody (YA6535) WB, IHC-P, IHC-F, ICC/IF, IF-Tissue, IP, FC Human

Related Diseases

Diseases Alias
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 E
  • Xeroderma Pigmentosum V

  • Xp5

  • Xeroderma Pigmentosum, Group E, Ddb-Negative Subtype

  • Xpe

  • Xp, Group E

  • Xeroderma Pigmentosum, Type 5

  • Xeroderma Pigmentosum Complementation Group E

  • XP-E

  • Xp Group E

Cockayne Syndrome
  • Cockayne'S Syndrome

  • Dwarfism-Retinal Atrophy-Deafness Syndrome

  • Neill-Dingwall Syndrome

  • Progeria-Like Syndrome

  • Progeroid Nanism

  • Cs

Xeroderma Pigmentosum Group E
  • Xeroderma Pigmentosum, Group E

  • Xeroderma Pigmentosum V

  • Xp Group E

  • Xp5

  • Xpe

  • Xeroderma Pigmentosum, Complementation Group E

Xeroderma Pigmentosum, Complementation Group C
  • Xeroderma Pigmentosum, Group C

  • XPC

  • Xpcc

  • Xeroderma Pigmentosum Iii

  • Xp3

  • Xeroderma Pigmentosum Group C

  • Xp Group C

  • Xp, Group C

  • Xeroderma Pigmentosum, Type 3

  • Xeroderma Pigmentosum Complementation Group C

  • XP-C

Childhood Medulloblastoma
  • Medulloblastoma, Childhood

  • Pediatric Medulloblastoma

  • Medulloblastoma Childhood

Cockayne Syndrome A
  • Cockayne Syndrome Type 1

  • Cockayne Syndrome, Type A

  • Cockayne Syndrome Type I

  • CSA

  • Cockayne Syndrome Classic Form

  • Cockayne Syndrome Classical

  • Cockayne Syndrome Type A

  • Ckn1

De Sanctis-Cacchione Syndrome
  • Xerodermic Idiocy

  • Xeroderma Pigmentosum With Neurologic Manifestation

  • DSC

  • Xerodermic Idiocy Of De Sanctis And Cacchione

Uv-Sensitive Syndrome
  • Uvss

  • Uv Sensitive Syndrome

  • Ultraviolet Sensitive Syndrome

Autosomal Recessive Intellectual Developmental Disorder
  • Mental Retardation, Autosomal Recessive

  • Autosomal Recessive Mental Retardation

  • Autosomal Recessive Non-Syndromic Mental Retardation

  • Autosomal Recessive Non-Syndromic Intellectual Disability

Three M Syndrome 1
  • 3-M Syndrome

  • Yakut Short Stature Syndrome

  • 3m Syndrome

  • Le Merrer Syndrome

  • Dolichospondylic Dysplasia

  • Gloomy Face Syndrome

  • Three M Syndrome

  • 3M1

  • 3m Syndrome 1

  • Miller-Mckusick-Malvaux Syndrome

  • 3-Msbn

  • Three-M Slender-Boned Nanism

  • Miller-Mckusick-Malvaux-Syndrome

  • 3-M Syndrome 1

  • 3m Syndrome-1

  • 3m Syndrome, Type 1

  • Dwarfism

  • Dwarfism Tall Vertebrae

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
Bos taurus CUL4A VGNC VGNC:27832
Rattus norvegicus CUL4A RGD RGD:1563853
Mus musculus CUL4A MGD MGI:1914487
Macaca mulatta CUL4A VGNC VGNC:71568
Felis catus CUL4A VGNC VGNC:97394
Canis familiaris CUL4A VGNC VGNC:39731
Others CUL4A NCBI