PSMD14 - proteasome 26S subunit, non-ATPase 14 Gene

Also Known as PAD1; POH1; RPN11

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10213

About PSMD14

Cytogenetic location: 2q24.2 Genomic coordinates (GRCh38): 2:161,308,425-161,411,717 (from NCBI)

This gene has 5 transcripts (splice variants), 211 orthologues and 3 paralogues. Ubiquitous expression in brain (RPKM 24.9), testis (RPKM 22.1) and 25 other tissues.

Summary

This gene encodes a component of the 26S Proteasome. The 26S Proteasome is a large multiprotein complex that catalyzes the degradation of ubiquitinated intracellular proteins. The encoded protein is a component of the 19S regulatory cap complex of the 26S Proteasome and mediates substrate deubiquitination. A pseudogene of this gene is also located on the long arm of chromosome 2. [provided by RefSeq, Feb 2012]

PSMD14 Products (1)

mRNA Protein Name
NM_005805.6 NP_005796.1 26S proteasome non-ATPase regulatory subunit 14
Molecular Function GO Annotation Evidence References Source
enables endopeptidase activator activity IMP
IMP: Inferred from mutant phenotype
18162577 GOA
enables metal-dependent deubiquitinase activity IMP
IMP: Inferred from mutant phenotype
22909820 GOA
enables proteasome binding IDA
IDA: Inferred from direct assay
18162577 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19615732 GOA
Biological Process GO Annotation Evidence References Source
involved in double-strand break repair via homologous recombination IMP
IMP: Inferred from mutant phenotype
22909820 GOA
involved in double-strand break repair via nonhomologous end joining IMP
IMP: Inferred from mutant phenotype
22909820 GOA
involved in protein K63-linked deubiquitination IMP
IMP: Inferred from mutant phenotype
22909820 GOA
involved in regulation of proteasomal protein catabolic process IMP
IMP: Inferred from mutant phenotype
18162577 GOA
Cellular Component GO Annotation Evidence References Source
part of proteasome complex IDA
IDA: Inferred from direct assay
17323924 GOA
part of proteasome regulatory particle, lid subcomplex IMP
IMP: Inferred from mutant phenotype
22909820 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

PSMD14 Protein Structure

JAB

JAB: JAB1/Mov34/MPN/PAD-1 ubiquitin protease (28 - 138)

MitMem_reg

MitMem_reg: Maintenance of mitochondrial structure and function (173 - 295)

  • 0
  • 100
  • 200
  • 310 a.a.
Protein Preferred Names Protein Names

26S proteasome non-ATPase regulatory subunit 14

  • 26S proteasome regulatory subunit rpn11

PSMD14 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PSMD14 O00487 FAM9B Homo sapiens Q8IZU0 25416956
Intra
PSMD14 O00487 FAM9B Homo sapiens Q8IZU0 25416956
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 25416956
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 32296183
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 25416956
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 32296183
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 25416956
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 26496610
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 19615732
Intra
PSMD14 O00487 PSMD7 Homo sapiens P51665 32296183
Intra
PSMD14 O00487 HTT Homo sapiens P42858 32814053
Intra
PSMD14 O00487 HTT Homo sapiens P42858 32814053
Intra
PSMD14 O00487 HTT Homo sapiens P42858 32814053
Intra
PSMD14 O00487 DPY30 Homo sapiens Q9C005 32296183
Intra
PSMD14 O00487 DPY30 Homo sapiens Q9C005 25416956
Intra
PSMD14 O00487 MEOX2 Homo sapiens P50222 25416956
Intra
PSMD14 O00487 MEOX2 Homo sapiens P50222 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

PSMD14 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82505 PSMD14 Antibody (YA2250) WB, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
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

Angelman Syndrome
  • AS

  • Happy Puppet Syndrome

  • Happy Puppet Syndrome, Formerly

  • Puppetlike 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

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

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 PSMD14 MGD MGI:1913284
Rattus norvegicus PSMD14 RGD RGD:1594532
Canis familiaris PSMD14 VGNC VGNC:45110
Felis catus PSMD14 VGNC VGNC:64415
Bos taurus PSMD14 VGNC VGNC:33465
Macaca mulatta PSMD14 VGNC VGNC:76269
Others PSMD14 NCBI