UBE2N - ubiquitin conjugating enzyme E2 N Gene

Also Known as UBC13; UbcH13; UBCHBEN; HEL-S-71; UbcH-ben; UBCHBEN; UBC13

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7334

About UBE2N

Cytogenetic location: 12q22 Genomic coordinates (GRCh38): 12:93,405,684-93,441,947 (from NCBI)

This gene has 6 transcripts (splice variants), 89 orthologues and 24 paralogues. Ubiquitous expression in testis (RPKM 18.8), brain (RPKM 12.2) and 25 other tissues.

Summary

The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating Enzymes, or E1s, ubiquitin-conjugating Enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. Studies in mouse suggest that this protein plays a role in DNA postreplication repair. [provided by RefSeq, Jul 2008]

UBE2N Products (1)

mRNA Protein Name
NM_003348.4 NP_003339.1 ubiquitin-conjugating enzyme E2 N
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
11473255 GOA
enables ubiquitin binding IDA
IDA: Inferred from direct assay
16122702 GOA
enables ubiquitin conjugating enzyme activity IDA
IDA: Inferred from direct assay
35927303 GOA
enables ubiquitin conjugating enzyme activity IMP
IMP: Inferred from mutant phenotype
17349954 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
18410486 GOA
enables ubiquitin-protein transferase activator activity IMP
IMP: Inferred from mutant phenotype
17349954 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
20061386 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of DNA double-strand break processing IMP
IMP: Inferred from mutant phenotype
17349954 GOA
involved in T cell receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
15125833 GOA
involved in antiviral innate immune response IDA
IDA: Inferred from direct assay
35893676 GOA
acts upstream of double-strand break repair via homologous recombination IMP
IMP: Inferred from mutant phenotype
17349954 GOA
involved in negative regulation of TORC1 signaling IDA
IDA: Inferred from direct assay
35927303 GOA
involved in positive regulation of DNA repair IMP
IMP: Inferred from mutant phenotype
16129784 GOA
involved in positive regulation of NF-kappaB transcription factor activity IMP
IMP: Inferred from mutant phenotype
14695475 GOA
involved in positive regulation of canonical NF-kappaB signal transduction IMP
IMP: Inferred from mutant phenotype
16129784 GOA
involved in positive regulation of double-strand break repair IDA
IDA: Inferred from direct assay
16129784 GOA
involved in positive regulation of intracellular signal transduction IDA
IDA: Inferred from direct assay
11057907 GOA
involved in positive regulation of protein K63-linked ubiquitination IDA
IDA: Inferred from direct assay
10089880 GOA
acts upstream of postreplication repair IMP
IMP: Inferred from mutant phenotype
17349954 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
35927303 GOA
involved in protein K63-linked ubiquitination IDA
IDA: Inferred from direct assay
16307917 GOA
involved in protein K63-linked ubiquitination IMP
IMP: Inferred from mutant phenotype
25936802 GOA
involved in protein monoubiquitination IMP
IMP: Inferred from mutant phenotype
17349954 GOA
involved in protein polyubiquitination IMP
IMP: Inferred from mutant phenotype
17349954 GOA
Cellular Component GO Annotation Evidence References Source
part of UBC13-MMS2 complex IDA
IDA: Inferred from direct assay
16129784 GOA
part of UBC13-MMS2 complex IPI
IPI: Inferred from physical interaction
11057907 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
19340006 GOA
located in cytosol IDA
IDA: Inferred from direct assay
16129784 GOA
located in nucleus IDA
IDA: Inferred from direct assay
16129784 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
22797923 GOA
part of ubiquitin conjugating enzyme complex IDA
IDA: Inferred from direct assay
17349954 GOA
part of ubiquitin ligase complex IDA
IDA: Inferred from direct assay
16307917 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

UBE2N Protein Structure

UQ_con

UQ_con: Ubiquitin-conjugating enzyme (7 - 142)

  • 0
  • 100
  • 152 a.a.
Protein Preferred Names Protein Names

ubiquitin-conjugating enzyme E2 N

  • E2 ubiquitin-conjugating enzyme N

UBE2N Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
UBE2N P61088 HLTF Homo sapiens Q14527 18719106
Intra
UBE2N P61088 UBE2V1 Homo sapiens Q13404 25260751
Intra
UBE2N P61088 UBE2V1 Homo sapiens Q13404 16307917
Intra
UBE2N P61088 UBE2V1 Homo sapiens Q13404
Y2H
19549727
Intra
UBE2N P61088 UBE2V1 Homo sapiens Q13404 11057907
Cross
UBE2N P61088 ORF169b Shigella flexneri Q8VSD5 22407319
Intra
UBE2N P61088 RFWD3 Homo sapiens Q6PCD5 25260751
Intra
UBE2N P61088 RNF13 Homo sapiens O43567 25260751
Intra
UBE2N P61088 RNF13 Homo sapiens O43567 19690564
Intra
UBE2N P61088 ZNRF1 Homo sapiens Q8ND25
TAP
27173435
Intra
UBE2N P61088 ZNRF1 Homo sapiens Q8ND25 19690564
Intra
UBE2N P61088 RNF182 Homo sapiens Q8N6D2 25260751
Cross
UBE2N P61088 otub-1 Caenorhabditis elegans Q9XVR6 22367539
Cross
UBE2N P61088 otub-1 Caenorhabditis elegans Q9XVR6
FPS
22367539
Intra
UBE2N P61088 STUB1 Homo sapiens Q9UNE7 16307917
Intra
UBE2N P61088 STUB1 Homo sapiens Q9UNE7 25260751
Intra
UBE2N P61088 TRAF6 Homo sapiens Q9Y4K3 19549727
Intra
UBE2N P61088 TRAF6 Homo sapiens Q9Y4K3
TAP
27173435
Intra
UBE2N P61088 TRAF6 Homo sapiens Q9Y4K3 19549727
Intra
UBE2N P61088 RNF11 Homo sapiens Q9Y3C5 19690564
Intra
UBE2N P61088 RNF11 Homo sapiens Q9Y3C5
Y2H
15231748
Intra
UBE2N P61088 XIAP Homo sapiens P98170 19549727
Intra
UBE2N P61088 XIAP Homo sapiens P98170 19549727
Intra
UBE2N P61088 XIAP Homo sapiens P98170 25260751
Intra
UBE2N P61088 BIRC3 Homo sapiens Q13489 19690564
Intra
UBE2N P61088 BIRC3 Homo sapiens Q13489 25260751
Intra
UBE2N P61088 UBE2V2 Homo sapiens Q15819
TAP
27173435
Intra
UBE2N P61088 UBE2V2 Homo sapiens Q15819
Y2H
19549727
Intra
UBE2N P61088 UBE2V2 Homo sapiens Q15819 11473255
Intra
UBE2N P61088 LRSAM1 Homo sapiens Q6UWE0 25260751
Intra
UBE2N P61088 LRSAM1 Homo sapiens Q6UWE0 19690564
Intra
UBE2N P61088 TRIM32 Homo sapiens Q13049
TAP
27173435
Intra
UBE2N P61088 RNF168 Homo sapiens Q8IYW5 19203578
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant UBE2N Proteins

Cat. No. Product Name Accession Purity
HY-P79452 UBE2N/Ubc13 Protein, Human (sf9, His, StrepII) P61088 (A2-I152) ≥ 90%, as determined by reducing SDS-PAGE.

UBE2N Antibodies

Cat. No. Product Name Application Reactivity
HY-P82233 Ubiquitin Conjugating Enzyme E2 N Antibody (YA1978) WB, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Riddle Syndrome
  • RIDL

  • Radiosensitivity-Immunodeficiency-Dysmorphic Features-Learning Difficulties Syndrome

  • Rnf168 Deficiency

  • Radiosensitivity, Immunodeficiency, Dysmorphic Facial Features, And Learning Difficulties

  • Radiosensitivity, Immunodeficiency, Dysmorphic Features, And Learning Difficulties

Machado-Joseph Disease
  • SCA3

  • MJD

  • Spinocerebellar Ataxia 3

  • Azorean Disease

  • Spinocerebellar Ataxia Type 3

  • Spinocerebellar Atrophy

  • Azorean Neurologic Disease

  • Spinopontine Atrophy

  • Nigrospinodentatal Degeneration

  • Spinocerebellar Atrophy Iii

  • Spinocerebellar Atrophy Type 3

  • Azorean Ataxia

  • Azorean Disease Of The Nervous System

  • Machado Disease

  • Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia

  • Disease, Machado-Joseph

  • Ataxia, Spinocerebellar

Limb-Girdle Muscular Dystrophy
  • Lgmd

  • Limb Girdle Muscular Dystrophy

  • Muscular Dystrophies, Limb-Girdle

  • Erb'S Muscular Dystrophy

  • Leyden-Mbius Muscular Dystrophy

  • Limb-Girdle Syndrome

  • Myopathic Limb-Girdle Syndrome

  • Limb Girdle

  • Muscular Dystrophy Limb-Girdle

  • Dystrophy, Muscular, Limb-Girdle

  • Lgmd - [Limb-Girdle Muscular Dystrophy]

  • Limb Girdle Muscle Dystrophy

  • Limb-Girdle Myopathy

Angelman Syndrome
  • AS

  • Happy Puppet Syndrome

  • Happy Puppet Syndrome, Formerly

  • Puppetlike Syndrome

Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

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

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

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
Mus musculus UBE2N MGD MGI:1934835
Rattus norvegicus UBE2N RGD RGD:621096
Macaca mulatta UBE2N VGNC VGNC:100116
Bos taurus UBE2N VGNC VGNC:36590
Others UBE2N NCBI