UBC - ubiquitin C Gene

Also Known as HMG20

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7316

About UBC

Cytogenetic location: 12q24.31 Genomic coordinates (GRCh38): 12:124,911,646-124,914,650 (from NCBI)

This gene has 13 transcripts (splice variants), 60 orthologues and 10 paralogues. Ubiquitous expression in bone marrow (RPKM 1559.8), gall bladder (RPKM 1270.7) and 25 other tissues.

Summary

This gene represents a ubiquitin gene, ubiquitin C. The encoded protein is a polyubiquitin precursor. Conjugation of ubiquitin monomers or Polymers can lead to various effects within a cell, depending on the residues to which ubiquitin is conjugated. Ubiquitination has been associated with protein degradation, DNA repair, cell cycle regulation, kinase modification, endocytosis, and regulation of Other cell signaling pathways. [provided by RefSeq, Aug 2010]

UBC Products (1)

mRNA Protein Name
NM_021009.7 NP_066289.3 polyubiquitin-C
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
8702753 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

UBC Protein Structure

ubiquitin

ubiquitin: Ubiquitin family (6 - 74)

ubiquitin

ubiquitin: Ubiquitin family (82 - 150)

ubiquitin

ubiquitin: Ubiquitin family (158 - 226)

ubiquitin

ubiquitin: Ubiquitin family (234 - 302)

ubiquitin

ubiquitin: Ubiquitin family (310 - 378)

ubiquitin

ubiquitin: Ubiquitin family (386 - 454)

ubiquitin

ubiquitin: Ubiquitin family (462 - 530)

ubiquitin

ubiquitin: Ubiquitin family (538 - 606)

ubiquitin

ubiquitin: Ubiquitin family (614 - 682)

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

polyubiquitin-C

UBC Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
UBC P0CG48 BUB1B Homo sapiens O60566 19407811
Intra
UBC P0CG48 MALT1 Homo sapiens Q9UDY8 17948050
Intra
UBC P0CG48 UBE2G2 Homo sapiens P60604 32296183
Intra
UBC P0CG48 UBE2G2 Homo sapiens P60604 32296183
Intra
UBC P0CG48 UBE2G2 Homo sapiens P60604 32296183
Intra
UBC P0CG48 UBE3A Homo sapiens Q05086-3 32296183
Intra
UBC P0CG48 UBE3A Homo sapiens Q05086-3 32296183
Intra
UBC P0CG48 UBE3A Homo sapiens Q05086-3 32296183
Intra
UBC P0CG48 FAM168A Homo sapiens Q92567-2 32296183
Intra
UBC P0CG48 MTURN Homo sapiens Q8N3F0 32296183
Intra
UBC P0CG48 EPN2 Homo sapiens O95208-2 32296183
Intra
UBC P0CG48 EPN2 Homo sapiens O95208-2 32296183
Intra
UBC P0CG48 LCK Homo sapiens P06239
NMR
18539162
Intra
UBC P0CG48 PRKCA Homo sapiens P17252 18566587
Cross
UBC P0CG48 RAD23 Saccharomyces cerevisiae P32628 20059542
Intra
UBC P0CG48 ABCG2 Homo sapiens Q9UNQ0 19909340
Intra
UBC P0CG48 NPLOC4 Homo sapiens Q8TAT6 35271311
Intra
UBC P0CG48 NPLOC4 Homo sapiens Q8TAT6
ITC
17070805
Intra
UBC P0CG48 BMI1 Homo sapiens P35226 20601937
Intra
UBC P0CG48 YOD1 Homo sapiens Q5VVQ6 32296183
Cross
UBC P0CG48 P0C6X7-PRO_0000037311 Human SARS coronavirus P0C6X7-PRO_0000037311 32726803
Cross
UBC P0CG48 P0C6X7-PRO_0000037311 Human SARS coronavirus P0C6X7-PRO_0000037311 32726803
Cross
UBC P0CG48 P0DTD1-PRO_0000449621 SARS-CoV-2 P0DTD1-PRO_0000449621 32726803
Cross
UBC P0CG48 P0DTD1-PRO_0000449621 SARS-CoV-2 P0DTD1-PRO_0000449621 32726803
Intra
UBC P0CG48 DESI1 Homo sapiens Q6ICB0 32296183
Intra
UBC P0CG48 POLH Homo sapiens Q9Y253
Y2H
16763556
Intra
UBC P0CG48 POLH Homo sapiens Q9Y253 16763556
Intra
UBC P0CG48 CDIP1 Homo sapiens Q9H305 32296183
Intra
UBC P0CG48 SENP3 Homo sapiens Q9H4L4 19680224
Intra
UBC P0CG48 SQSTM1 Homo sapiens Q13501 12857745
Intra
UBC P0CG48 SQSTM1 Homo sapiens Q13501 8702753
Intra
UBC P0CG48 SQSTM1 Homo sapiens Q13501 19427866
Intra
UBC P0CG48 NFKBIA Homo sapiens P25963 17318178
Intra
UBC P0CG48 NFKBIA Homo sapiens P25963 17318178
Intra
UBC P0CG48 NFKBIA Homo sapiens P25963 18539148
Intra
UBC P0CG48 ASAP2 Homo sapiens O43150 17255943
Intra
UBC P0CG48 SH3KBP1 Homo sapiens Q96B97
NMR
19111555
Intra
UBC P0CG48 SH3KBP1 Homo sapiens Q96B97
NMR
18680311
Intra
UBC P0CG48 ASAP1 Homo sapiens Q9ULH1 17255943
Intra
UBC P0CG48 ASAP1 Homo sapiens Q9ULH1 17255943
Intra
UBC P0CG48 PARP1 Homo sapiens P09874 19779455
Intra
UBC P0CG48 PARP1 Homo sapiens P09874 19779455
Intra
UBC P0CG48 MAP3K7 Homo sapiens O43318 19820695
Intra
UBC P0CG48 MAP3K7 Homo sapiens O43318 16845370
Intra
UBC P0CG48 MAP3K7 Homo sapiens O43318 19820695
Intra
UBC P0CG48 TRAF6 Homo sapiens Q9Y4K3 17703191
Intra
UBC P0CG48 PSMD4 Homo sapiens P55036 20059542
Intra
UBC P0CG48 PSMD4 Homo sapiens P55036 9488668
Intra
UBC P0CG48 PSMD4 Homo sapiens P55036 8570649
Intra
UBC P0CG48 PSMD4 Homo sapiens P55036
SPR
19798103
Intra
UBC P0CG48 PSMD4 Homo sapiens P55036 19796170
Intra
UBC P0CG48 TP53 Homo sapiens P04637 17170702
Intra
UBC P0CG48 TP53 Homo sapiens P04637 17159902
Intra
UBC P0CG48 TP53 Homo sapiens P04637 18566590
Intra
UBC P0CG48 TP53 Homo sapiens P04637 18309296
Intra
UBC P0CG48 TP53 Homo sapiens P04637 17139261
Intra
UBC P0CG48 TP53 Homo sapiens P04637 17568776
Intra
UBC P0CG48 TP53 Homo sapiens P04637 18388957
Intra
UBC P0CG48 TP53 Homo sapiens P04637 19619542
Intra
UBC P0CG48 TP53 Homo sapiens P04637 18566590
Intra
UBC P0CG48 TP53 Homo sapiens P04637 17268548
Intra
UBC P0CG48 PLEKHB2 Homo sapiens Q96CS7 32296183
Intra
UBC P0CG48 ELAVL1 Homo sapiens Q15717 19322201
Intra
UBC P0CG48 MDM2 Homo sapiens Q00987 18566590
Intra
UBC P0CG48 MDM2 Homo sapiens Q00987 19166840
Intra
UBC P0CG48 MDM2 Homo sapiens Q00987 18566590
Intra
UBC P0CG48 MDM2 Homo sapiens Q00987 19098711
Intra
UBC P0CG48 GRK2 Homo sapiens P25098 17006543
Intra
UBC P0CG48 NFATC4 Homo sapiens Q14934 19026640
Intra
UBC P0CG48 NFATC4 Homo sapiens Q14934 19026640
Intra
UBC P0CG48 RDH12 Homo sapiens Q96NR8 20006610
Intra
UBC P0CG48 MYC Homo sapiens P01106 19131971
Intra
UBC P0CG48 MAP3K4 Homo sapiens Q9Y6R4 16256071
Intra
UBC P0CG48 MAP3K4 Homo sapiens Q9Y6R4 16256071
Intra
UBC P0CG48 HTT Homo sapiens P42858 32814053
Intra
UBC P0CG48 HTT Homo sapiens P42858 32814053
Intra
UBC P0CG48 HTT Homo sapiens P42858 32814053
Intra
UBC P0CG48 XIAP Homo sapiens P98170 17318174
Intra
UBC P0CG48 XIAP Homo sapiens P98170 17318174
Intra
UBC P0CG48 XIAP Homo sapiens P98170 17318174
Intra
UBC P0CG48 TAX1BP1 Homo sapiens Q86VP1 32296183
Intra
UBC P0CG48 TAX1BP1 Homo sapiens Q86VP1 32296183
Intra
UBC P0CG48 TAX1BP1 Homo sapiens Q86VP1 18239685
Intra
UBC P0CG48 TAX1BP1 Homo sapiens Q86VP1 32296183
Intra
UBC P0CG48 BCL2L12 Homo sapiens Q9HB09-1 19376117
Intra
UBC P0CG48 BCL2L12 Homo sapiens Q9HB09-1 19376117
Intra
UBC P0CG48 NCK2 Homo sapiens O43639
NMR
18539162
Intra
UBC P0CG48 DENR Homo sapiens O43583 16936636
Intra
UBC P0CG48 DENR Homo sapiens O43583 16874301
Intra
UBC P0CG48 DENR Homo sapiens O43583 16936636
Intra
UBC P0CG48 DAZAP2 Homo sapiens Q15038 32296183
Intra
UBC P0CG48 DAZAP2 Homo sapiens Q15038 32296183
Intra
UBC P0CG48 DAZAP2 Homo sapiens Q15038 32296183
Intra
UBC P0CG48 CSF3R Homo sapiens Q99062 17363902
Intra
UBC P0CG48 CSF3R Homo sapiens Q99062 17363902
Intra
UBC P0CG48 RELA Homo sapiens Q04206 17183367
Intra
UBC P0CG48 RELA Homo sapiens Q04206 17183367
Intra
UBC P0CG48 RELA Homo sapiens Q04206 19322197
Intra
UBC P0CG48 RELA Homo sapiens Q04206 19322197
Intra
UBC P0CG48 POLI Homo sapiens Q9UNA4
Y2H
16763556
Intra
UBC P0CG48 NBR1 Homo sapiens Q14596 24879152
Intra
UBC P0CG48 NBR1 Homo sapiens Q14596 19427866
Intra
UBC P0CG48 NBR1 Homo sapiens Q14596
IF
19427866
Intra
UBC P0CG48 UBAC1 Homo sapiens Q9BSL1 32296183
Intra
UBC P0CG48 RYBP Homo sapiens Q8N488
ITC
17070805
Intra
UBC P0CG48 STAM Homo sapiens Q92783
NMR
12750381
Intra
UBC P0CG48 STAM Homo sapiens Q92783
SPR
12750381
Intra
UBC P0CG48 STAM Homo sapiens Q92783
NMR
19111546
Intra
UBC P0CG48 PLSCR4 Homo sapiens Q9NRQ2 32296183
Intra
UBC P0CG48 DAXX Homo sapiens Q9UER7 20936779
Intra
UBC P0CG48 SNX9 Homo sapiens Q9Y5X1 20491914
Intra
UBC P0CG48 ZFAND5 Homo sapiens O76080 16424905
Intra
UBC P0CG48 ATXN3 Homo sapiens P54252-1 19153604
Intra
UBC P0CG48 ATXN3 Homo sapiens P54252-1 19153604
Intra
UBC P0CG48 ATXN3 Homo sapiens P54252-1 14559776
Intra
UBC P0CG48 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
UBC P0CG48 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
UBC P0CG48 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
UBC P0CG48 ADRM1 Homo sapiens Q16186 20059542
Intra
UBC P0CG48 RAD23B Homo sapiens P54727 20059542
Intra
UBC P0CG48 RAD23B Homo sapiens P54727 32296183
Cross
UBC P0CG48 Ikbkg Mus musculus O88522 19763089
Cross
UBC P0CG48 rev Human immunodeficiency virus P04325 17067581
Cross
UBC P0CG48 Rbck1 Rattus norvegicus Q62921 19796170
Cross
UBC P0CG48 Rbck1 Rattus norvegicus Q62921 19796170
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Phlyctenulosis
  • Phlyctenular Keratoconjunctivitis

  • Strumous Ophthalmia

Middle East Respiratory Syndrome
  • Mers

  • Mers - [Middle East Respiratory Syndrome]

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

Paget'S Disease Of Bone
  • Osteitis Deformans

  • Paget Disease Of Bone

  • Osseous Paget'S Disease

  • Paget Disease Of Bone, Familial

  • Bone Paget Disease

  • Familial Paget'S Disease Of Bone

  • Paget'S Bone Disease

  • Familial Paget Disease Of Bone

  • Paget Disease, Bone

  • Pdb

  • Pagets Bone Disease

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Myoclonic Epilepsy Of Lafora
  • Lafora Disease

  • Epilepsy, Progressive Myoclonic 2b

  • EPM2

  • Melf

  • Epilepsy, Progressive Myoclonic 2a

  • Epm2a

  • Lafora'S Disease

  • Lafora Body Disease

  • Lbd

  • Epilepsy, Progressive Myoclonic, 2a

  • Lafora Progressive Myoclonic Epilepsy

  • Epilepsy Progressive Myoclonic 2

  • Lafora Body Disorder

  • Pme Type 2

  • Progressive Myoclonic Epilepsy Type 2

  • Progressive Myoclonus Epilepsy Type 2

  • Epilepsy, Progressive Myoclonic 2

  • Epm2b

  • Ld

  • Progressive Myoclonic Epilepsy 2

  • Progressive Myoclonic Epilepsy 2a

  • Progressive Myoclonic Epilepsy 2b

  • Progressive Myoclonic Epilepsy Lafora Type

  • Epilepsy, Myoclonic, Of Lafora

Epilepsy
  • Epilepsy Syndrome

  • Epileptic Syndrome

  • Epilepsies

  • Symptomatic Epilepsies

  • Post Traumatic Epilepsy

  • Traumatic Epilepsy

  • Traumatic Epileptic

  • Epilepsy Due To Hippocampal Sclerosis

  • Epilepsy With Ammon'S Horn Sclerosis

  • Epilepsy Due To Cortical Dysplasia

  • Epilepsy Due To Neuronal Migration Disorders

Ectodermal Dysplasia
  • Congenital Ectodermal Defect

  • Congenital Ectodermal Dysplasia

  • Ectodermal Dysplasia Syndrome

  • Dysplasia, Ectodermal

Angelman Syndrome
  • AS

  • Happy Puppet Syndrome

  • Happy Puppet Syndrome, Formerly

  • Puppetlike Syndrome

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

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 UBC MGD MGI:98889
Rattus norvegicus UBC RGD RGD:621244
Bos taurus UBC VGNC VGNC:107263
Others UBC NCBI