OTUD4 - OTU deubiquitinase 4 Gene

Also Known as HIN1; DUBA6; HSHIN1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 54726

About OTUD4

Cytogenetic location: 4q31.21 Genomic coordinates (GRCh38): 4:145,133,650-145,180,589 (from NCBI)

This gene has 10 transcripts (splice variants), 146 orthologues and 5 paralogues. Ubiquitous expression in testis (RPKM 19.7), bone marrow (RPKM 11.0) and 25 other tissues.

Summary

Alternatively spliced transcript variants have been found for this gene. The smaller protein isoform encoded by the shorter transcript variant is found only in HIV-1 infected cells. [provided by RefSeq, Jul 2010]

OTUD4 Products (4)

mRNA Protein Name
NM_001102653.1 NP_001096123.1 OTU domain-containing protein 4 isoform 3
NM_001366057.1 NP_001352986.1 OTU domain-containing protein 4 isoform 4
NM_001366058.1 NP_001352987.1 OTU domain-containing protein 4 isoform 5
NM_017493.7 NP_059963.1 OTU domain-containing protein 4 isoform 2
Molecular Function GO Annotation Evidence Verweise Source
enables K63-linked deubiquitinase activity IDA
IDA: Inferred from direct assay
29395066 GOA
enables cysteine-type deubiquitinase activity IDA
IDA: Inferred from direct assay
23827681 GOA
enables molecular adaptor activity IDA
IDA: Inferred from direct assay
25944111 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in DNA alkylation repair IDA
IDA: Inferred from direct assay
25944111 GOA
involved in negative regulation of interleukin-1-mediated signaling pathway IDA
IDA: Inferred from direct assay
29395066 GOA
involved in negative regulation of toll-like receptor signaling pathway IDA
IDA: Inferred from direct assay
29395066 GOA
involved in protein K11-linked deubiquitination IDA
IDA: Inferred from direct assay
36943869 GOA
involved in protein K48-linked deubiquitination IDA
IDA: Inferred from direct assay
23827681 GOA
involved in protein K63-linked deubiquitination IDA
IDA: Inferred from direct assay
29395066 GOA
involved in regulation of protein K48-linked deubiquitination IDA
IDA: Inferred from direct assay
25944111 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

OTUD4 Protein Structure

OTU

OTU: OTU-like cysteine protease (41 - 149)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1114 a.a.
Protein Preferred Names Protein Names

OTU domain-containing protein 4

  • HIV-1 induced protein HIN-1

OTUD4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
OTUD4 Q01804 STAT1 Homo sapiens P42224 25416956
Intra
OTUD4 Q01804 VDR Homo sapiens P11473-2 32296183
Intra
OTUD4 Q01804 VDR Homo sapiens P11473-2 32296183
Intra
OTUD4 Q01804 REL Homo sapiens Q04864 25416956
Intra
OTUD4 Q01804 REL Homo sapiens Q04864 25416956
Intra
OTUD4 Q01804 REL Homo sapiens Q04864 25416956
Intra
OTUD4 Q01804 EXOSC8 Homo sapiens Q96B26 32296183
Intra
OTUD4 Q01804 EXOSC8 Homo sapiens Q96B26 32296183
Intra
OTUD4 Q01804 EXOSC8 Homo sapiens Q96B26 32296183
Intra
OTUD4 Q01804 TCF4 Homo sapiens P15884 25416956
Intra
OTUD4 Q01804 TCF4 Homo sapiens P15884 25416956
Intra
OTUD4 Q01804 ZNF655 Homo sapiens Q8N720 32296183
Intra
OTUD4 Q01804 ZNF655 Homo sapiens Q8N720 32296183
Intra
OTUD4 Q01804 ZNF655 Homo sapiens Q8N720 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

OTUD4 Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P84460 OTUD4 Antibody (YA4157) WB, FC, ELISA Human, Rat
HY-P84460A OTUD4 Antibody (YA4157)(PBS only) WB, FC, ELISA Human, Rat

Related Diseases

Diseases Alias
Boucher-Neuhauser Syndrome
  • Ataxia-Hypogonadism-Choroidal Dystrophy Syndrome

  • BNHS

  • Spinocerebellar Ataxia, Hypogonadotropic Hypogonadism, And Chorioretinal Dystrophy

  • Boucher-Neuhäuser Syndrome

  • Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism

  • Ataxia - Hypogonadism - Choroidal Dystrophy

  • Chorioretinal Dystrophy, Spinocerebellar Ataxia And Hypogonadotropic Hypogonadism

  • Bns

  • Cerebellar Ataxia With Hypogonadism And Choroidal Dystrophy Syndrome

  • Boucher Neuhauser Syndrome

Gordon Holmes Syndrome
  • Cerebellar Ataxia And Hypogonadotropic Hypogonadism

  • Lhrh Deficiency And Ataxia

  • Cerebellar Ataxia-Hypogonadism Syndrome

  • GDHS

  • Cahh

  • Luteinizing Hormone-Releasing Hormone Deficiency With Ataxia

  • Gordon-Holmes Syndrome

  • Deficiency Of Luteinizing Hormone-Releasing Hormone With Ataxia

  • Luteinizing Hormone-Releasing Hormone, Deficiency Of, With Ataxia

  • Cerebellar Ataxia - Hypogonadism

  • Luteinizing Hormone Releasing Hormone, Deficiency Of With Ataxia

  • Ataxia, Cerebellar, And Hypogonadotropic Hypogonadism

Nivelon-Nivelon-Mabille Syndrome
  • Chondrodysplasia-Pseudohermaphroditism Syndrome

  • NNMS

  • Chondrodysplasia-Disorder Of Sex Development Syndrome

  • Nivelon Nivelon Mabille Syndrome

Spinocerebellar Ataxia, Autosomal Recessive 16
  • Autosomal Recessive Spinocerebellar Ataxia 16

  • SCAR16

  • Autosomal Recessive Cerebellar Ataxia Due To Stub1 Deficiency

  • Spinocerebellar Ataxia Autosomal Recessive Type 16

  • Spinocerebellar Ataxia, Autosomal Recessive, 16

  • Ataxia, Spinocerebellar, Autosomal Recessive, Type 16

Spinocerebellar Ataxia, Autosomal Recessive 24
  • SCAR24

  • Autosomal Recessive Spinocerebellar Ataxia 24

  • Spinocerebellar Ataxia, Autosomal Recessive, 24

  • Ataxia, Spinocerebellar, Autosomal Recessive, Type 24

Kallmann Syndrome
  • Hypogonadism With Anosmia

  • Kallman'S Syndrome

  • Anosmic Hypogonadism

  • Anosmic Idiopathic Hypogonadotropic Hypogonadism

  • Hypogonadotropic Hypogonadism And Anosmia

  • Hypogonadotropic Hypogonadism-Anosmia Syndrome

  • Olfacto-Genital Pathological Sequence

  • Familial Hypogonadism With Anosmia

  • Kallman Syndrome

  • Dysplasia Olfactogenitalis Of De Morsier

  • Kallmann'S Syndrome

  • Congenital Hypogonadotropic Hypogonadism With Anosmia

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
Macaca mulatta OTUD4 VGNC VGNC:75675
Mus musculus OTUD4 MGD MGI:1098801
Felis catus OTUD4 VGNC VGNC:64000
Rattus norvegicus OTUD4 RGD RGD:1305606
Bos taurus OTUD4 VGNC VGNC:32495
Canis familiaris OTUD4 VGNC VGNC:44186
Others OTUD4 NCBI