UBXN7 - UBX domain protein 7 Gene

Also Known as UBXD7

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 26043

About UBXN7

Cytogenetic location: 3q29 Genomic coordinates (GRCh38): 3:196,347,662-196,432,427 (from NCBI)

This gene has 6 transcripts (splice variants), 174 orthologues and 4 paralogues. Ubiquitous expression in bone marrow (RPKM 8.3), testis (RPKM 7.0) and 25 other tissues.

Summary

Enables ubiquitin binding activity and ubiquitin protein Ligase binding activity. Located in nuclear body. Part of VCP-NPL4-UFD1 AAA ATPase complex. [provided by Alliance of Genome Resources, Apr 2022]

UBXN7 Products (1)

mRNA Protein Name
NM_015562.2 NP_056377.1 UBX domain-containing protein 7
Molecular Function GO Annotation Evidence References Source
enables RNA polymerase II-specific DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
18775313 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
18775313 GOA
enables ubiquitin binding IDA
IDA: Inferred from direct assay
18775313 GOA
enables ubiquitin protein ligase binding IDA
IDA: Inferred from direct assay
18775313 GOA
Cellular Component GO Annotation Evidence References Source
part of VCP-NPL4-UFD1 AAA ATPase complex IDA
IDA: Inferred from direct assay
18775313 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

UBXN7 Protein Structure

UBA_4

UBA_4: UBA-like domain (16 - 54)

Thioredoxin_7

Thioredoxin_7: Thioredoxin-like (153 - 233)

UBX

UBX: UBX domain (410 - 486)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 489 a.a.
Protein Preferred Names Protein Names

UBX domain-containing protein 7

  • UBX domain containing 7

UBXN7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
UBXN7 O94888 REL Homo sapiens Q04864-2 32296183
Intra
UBXN7 O94888 REL Homo sapiens Q04864-2 32296183
Intra
UBXN7 O94888 REL Homo sapiens Q04864-2 32296183
Intra
UBXN7 O94888 TRIM39 Homo sapiens Q9HCM9-2 32296183
Intra
UBXN7 O94888 TRIM39 Homo sapiens Q9HCM9-2 32296183
Intra
UBXN7 O94888 TRIM39 Homo sapiens Q9HCM9-2 32296183
Intra
UBXN7 O94888 NFYC Homo sapiens Q13952-2 32296183
Intra
UBXN7 O94888 NFYC Homo sapiens Q13952-2 32296183
Intra
UBXN7 O94888 NFYC Homo sapiens Q13952-2 32296183
Intra
UBXN7 O94888 FAM168A Homo sapiens Q92567-2 32296183
Intra
UBXN7 O94888 FAM168A Homo sapiens Q92567-2 32296183
Intra
UBXN7 O94888 FAM168A Homo sapiens Q92567-2 32296183
Intra
UBXN7 O94888 CLEC19A Homo sapiens Q6UXS0 32296183
Intra
UBXN7 O94888 CLEC19A Homo sapiens Q6UXS0 32296183
Intra
UBXN7 O94888 CLEC19A Homo sapiens Q6UXS0 32296183
Cross
UBXN7 O94888 Cul1 Mus musculus Q9WTX6 22466964
Intra
UBXN7 O94888 ZNRF1 Homo sapiens Q8ND25 32296183
Intra
UBXN7 O94888 ZNRF1 Homo sapiens Q8ND25 32296183
Intra
UBXN7 O94888 ZNRF1 Homo sapiens Q8ND25 32296183
Intra
UBXN7 O94888 TRIM8 Homo sapiens Q9BZR9 32296183
Intra
UBXN7 O94888 TRIM8 Homo sapiens Q9BZR9 32296183
Intra
UBXN7 O94888 TRIM8 Homo sapiens Q9BZR9 32296183
Intra
UBXN7 O94888 MEOX1 Homo sapiens P50221 32296183
Intra
UBXN7 O94888 MEOX1 Homo sapiens P50221 32296183
Intra
UBXN7 O94888 MEOX1 Homo sapiens P50221 32296183
Intra
UBXN7 O94888 PAX5 Homo sapiens Q02548 32296183
Intra
UBXN7 O94888 PAX5 Homo sapiens Q02548 32296183
Intra
UBXN7 O94888 PAX5 Homo sapiens Q02548 32296183
Intra
UBXN7 O94888 VCP Homo sapiens P55072 33961781
Intra
UBXN7 O94888 VCP Homo sapiens P55072 18775313
Intra
UBXN7 O94888 VCP Homo sapiens P55072 32296183
Intra
UBXN7 O94888 VCP Homo sapiens P55072 22466964
Intra
UBXN7 O94888 VCP Homo sapiens P55072 32296183
Intra
UBXN7 O94888 VCP Homo sapiens P55072 32296183
Intra
UBXN7 O94888 TRAF6 Homo sapiens Q9Y4K3 32296183
Intra
UBXN7 O94888 TRAF6 Homo sapiens Q9Y4K3 32296183
Intra
UBXN7 O94888 TRAF6 Homo sapiens Q9Y4K3 32296183
Intra
UBXN7 O94888 CUL1 Homo sapiens Q13616 18775313
Intra
UBXN7 O94888 CUL1 Homo sapiens Q13616 22466964
Intra
UBXN7 O94888 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
UBXN7 O94888 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
UBXN7 O94888 HIF1A Homo sapiens Q16665 18775313
Intra
UBXN7 O94888 CUL4B Homo sapiens Q13620 18775313
Intra
UBXN7 O94888 CUL4B Homo sapiens Q13620 22466964
Intra
UBXN7 O94888 CUL4A Homo sapiens Q13619 22466964
Intra
UBXN7 O94888 CUL4A Homo sapiens Q13619 18775313
Intra
UBXN7 O94888 CUL3 Homo sapiens Q13618 22466964
Intra
UBXN7 O94888 CUL3 Homo sapiens Q13618 18775313
Intra
UBXN7 O94888 CUL2 Homo sapiens Q13617 18775313
Intra
UBXN7 O94888 CUL2 Homo sapiens Q13617 22466964
Intra
UBXN7 O94888 TRIM62 Homo sapiens Q9BVG3 32296183
Intra
UBXN7 O94888 TRIM62 Homo sapiens Q9BVG3 32296183
Intra
UBXN7 O94888 TRIM62 Homo sapiens Q9BVG3 32296183
Intra
UBXN7 O94888 NEDD8 Homo sapiens Q15843 22466964
Intra
UBXN7 O94888 DAZAP2 Homo sapiens Q15038 32296183
Intra
UBXN7 O94888 DAZAP2 Homo sapiens Q15038 32296183
Intra
UBXN7 O94888 DAZAP2 Homo sapiens Q15038 32296183
Intra
UBXN7 O94888 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
UBXN7 O94888 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
UBXN7 O94888 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
UBXN7 O94888 PAX6 Homo sapiens P26367 32296183
Intra
UBXN7 O94888 PAX6 Homo sapiens P26367 32296183
Intra
UBXN7 O94888 PAX6 Homo sapiens P26367 32296183
Intra
UBXN7 O94888 CRX Homo sapiens O43186 32296183
Intra
UBXN7 O94888 CRX Homo sapiens O43186 32296183
Intra
UBXN7 O94888 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
UBXN7 O94888 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
UBXN7 O94888 UBQLN2 Homo sapiens Q9UHD9 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Immunodeficiency 46
  • Tfrc-Related Combined Immunodeficiency

  • IMD46

  • Cid Due To Tfrc Deficiency

  • Combined Immunodeficiency Due To Tfrc Deficiency

Chromosome 3q29 Deletion Syndrome
  • Chromosome 3q29 Microdeletion Syndrome

  • 3q29 Microdeletion Syndrome

  • 3q Subtelomere Deletion Syndrome

  • 3q29 Recurrent Deletion

  • 3qter Deletion

  • 3q29 Deletion Syndrome

  • Monosomy 3q29

  • Microdeletion 3q29 Syndrome

  • Del(3)(Q29)

  • Monosomy 3qter

  • 3q29 Deletion

  • Del3q29

Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia
  • Ibmpfd

  • Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia

  • Pagetoid Amyotrophic Lateral Sclerosis

  • Pagetoid Neuroskeletal Syndrome

  • Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia

  • Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia

  • Multisystem Proteinopathy

  • Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone

  • Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia

  • Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement

  • Lower Motor Neuron Degeneration With Paget-Like Bone Disease

  • Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone

  • Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia

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 UBXN7 VGNC VGNC:36629
Rattus norvegicus UBXN7 RGD RGD:1306346
Macaca mulatta UBXN7 VGNC VGNC:79778
Canis familiaris UBXN7 VGNC VGNC:48102
Felis catus UBXN7 VGNC VGNC:102862
Mus musculus UBXN7 MGD MGI:2146388
Others UBXN7 NCBI