TRIM37 - tripartite motif containing 37 Gene

Also Known as MUL; POB1; TEF3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4591

About TRIM37

Cytogenetic location: 17q22 Genomic coordinates (GRCh38): 17:58,967,201-59,106,880 (from NCBI)

This gene has 14 transcripts (splice variants), 206 orthologues, 80 paralogues and is associated with 3 phenotypes. Broad expression in testis (RPKM 19.8), brain (RPKM 14.1) and 23 other tissues.

Summary

This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. Mutations in this gene are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. TRIM37 localizes in peroxisomal membranes, and has been implicated in human peroxisomal biogenesis disorders. [provided by RefSeq, Jul 2020]

TRIM37 Products (11)

mRNA Protein Name
NM_001005207.5 NP_001005207.1 E3 ubiquitin-protein ligase TRIM37 isoform a
NM_001320987.3 NP_001307916.1 E3 ubiquitin-protein ligase TRIM37 isoform b
NM_001320988.3 NP_001307917.1 E3 ubiquitin-protein ligase TRIM37 isoform c
NM_001320989.3 NP_001307918.1 E3 ubiquitin-protein ligase TRIM37 isoform c
NM_001320990.3 NP_001307919.1 E3 ubiquitin-protein ligase TRIM37 isoform d
NM_001353082.2 NP_001340011.1 E3 ubiquitin-protein ligase TRIM37 isoform e
NM_001353083.2 NP_001340012.1 E3 ubiquitin-protein ligase TRIM37 isoform f
NM_001353084.2 NP_001340013.1 E3 ubiquitin-protein ligase TRIM37 isoform g
NM_001353085.2 NP_001340014.1 E3 ubiquitin-protein ligase TRIM37 isoform h
NM_001353086.2 NP_001340015.1 E3 ubiquitin-protein ligase TRIM37 isoform i
NM_015294.6 NP_056109.1 E3 ubiquitin-protein ligase TRIM37 isoform a
Molecular Function GO Annotation Evidence References Source
enables histone H2AK119 ubiquitin ligase activity IDA
IDA: Inferred from direct assay
25470042 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11279055 GOA
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
11279055 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
23077300 GOA
enables tumor necrosis factor receptor binding IPI
IPI: Inferred from physical interaction
11279055 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
28724525 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
11279055 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
15885686 GOA
Biological Process GO Annotation Evidence References Source
involved in aggresome assembly IDA
IDA: Inferred from direct assay
15885686 GOA
involved in negative regulation of NF-kappaB transcription factor activity IDA
IDA: Inferred from direct assay
11279055 GOA
involved in negative regulation of centriole replication IMP
IMP: Inferred from mutant phenotype
23769972 GOA
involved in negative regulation of gene expression, epigenetic IDA
IDA: Inferred from direct assay
25470042 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
25470042 GOA
involved in positive regulation of DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
23077300 GOA
involved in positive regulation of NF-kappaB transcription factor activity IDA
IDA: Inferred from direct assay
23077300 GOA
involved in protein autoubiquitination IDA
IDA: Inferred from direct assay
15885686 GOA
acts upstream of protein import into peroxisome matrix IDA
IDA: Inferred from direct assay
28724525 GOA
involved in protein monoubiquitination IDA
IDA: Inferred from direct assay
28724525 GOA
involved in protein stabilization IDA
IDA: Inferred from direct assay
28724525 GOA
Cellular Component GO Annotation Evidence References Source
part of ESC/E(Z) complex IDA
IDA: Inferred from direct assay
25470042 GOA
located in aggresome IDA
IDA: Inferred from direct assay
15885686 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
23769972 GOA
located in cytosol IDA
IDA: Inferred from direct assay
11279055 GOA
is active in peroxisomal membrane IDA
IDA: Inferred from direct assay
28724525 GOA
located in peroxisome IDA
IDA: Inferred from direct assay
11938494 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

TRIM37 Protein Structure

zf-B_box

zf-B_box: B-box zinc finger (91 - 132)

MATH

MATH: MATH domain (284 - 403)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 964 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase TRIM37

  • RING-B-box-coiled-coil protein

TRIM37 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TRIM37 O94972 a8k932_human Homo sapiens A8K932 25416956
Intra
TRIM37 O94972 a8k932_human Homo sapiens A8K932 25416956
Intra
TRIM37 O94972 FAM107A Homo sapiens O95990-3 25416956
Intra
TRIM37 O94972 FAM107A Homo sapiens O95990-3 25416956
Intra
TRIM37 O94972 FAM107A Homo sapiens O95990-3 25416956
Intra
TRIM37 O94972 CDC20B Homo sapiens Q86Y33 25416956
Intra
TRIM37 O94972 DZIP1L Homo sapiens Q8IYY4 32296183
Intra
TRIM37 O94972 PNKP Homo sapiens Q96T60 16189514
Intra
TRIM37 O94972 PNKP Homo sapiens Q96T60 32296183
Intra
TRIM37 O94972 PNKP Homo sapiens Q96T60 38225382
Intra
TRIM37 O94972 TCEANC Homo sapiens Q8N8B7-2 32296183
Intra
TRIM37 O94972 CDC20B Homo sapiens Q86Y33-5 32296183
Intra
TRIM37 O94972 UBASH3A Homo sapiens P57075 25416956
Intra
TRIM37 O94972 UBASH3A Homo sapiens P57075 25416956
Intra
TRIM37 O94972 UBASH3A Homo sapiens P57075 25416956
Intra
TRIM37 O94972 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
TRIM37 O94972 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
TRIM37 O94972 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
TRIM37 O94972 ZMAT2 Homo sapiens Q96NC0 25416956
Intra
TRIM37 O94972 MCRS1 Homo sapiens Q96EZ8 25416956
Intra
TRIM37 O94972 MCRS1 Homo sapiens Q96EZ8 16189514
Intra
TRIM37 O94972 DDX6 Homo sapiens P26196 25416956
Intra
TRIM37 O94972 DDX6 Homo sapiens P26196 25416956
Intra
TRIM37 O94972 BYSL Homo sapiens Q13895 25416956
Intra
TRIM37 O94972 BYSL Homo sapiens Q13895 32296183
Intra
TRIM37 O94972 COPB1 Homo sapiens P53618 32296183
Intra
TRIM37 O94972 CDKL3 Homo sapiens Q8IVW4 32296183
Intra
TRIM37 O94972 CWF19L2 Homo sapiens Q2TBE0 32296183
Intra
TRIM37 O94972 ZNF587 Homo sapiens Q96SQ5 32296183
Intra
TRIM37 O94972 FAM161A Homo sapiens Q3B820 25416956
Intra
TRIM37 O94972 FAM161A Homo sapiens Q3B820 25416956
Intra
TRIM37 O94972 ZNF417 Homo sapiens Q8TAU3 25416956
Intra
TRIM37 O94972 ZNF417 Homo sapiens Q8TAU3 25416956
Intra
TRIM37 O94972 ZNF417 Homo sapiens Q8TAU3 25416956
Intra
TRIM37 O94972 ZNF417 Homo sapiens Q8TAU3 16189514
Intra
TRIM37 O94972 RASD1 Homo sapiens Q9Y272 25416956
Intra
TRIM37 O94972 RASD1 Homo sapiens Q9Y272 25416956
Intra
TRIM37 O94972 RASD1 Homo sapiens Q9Y272 25416956
Intra
TRIM37 O94972 PRC1 Homo sapiens O43663 16189514
Intra
TRIM37 O94972 ELOA Homo sapiens Q14241 32296183
Intra
TRIM37 O94972 FAM50B Homo sapiens Q9Y247 25416956
Intra
TRIM37 O94972 AQP1 Homo sapiens P29972 32296183
Intra
TRIM37 O94972 SYTL4 Homo sapiens Q96C24 32296183
Intra
TRIM37 O94972 SCNM1 Homo sapiens Q9BWG6 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

TRIM37 Antibodies

Cat. No. Product Name Application Reactivity
HY-P89595 TRIM37 Antibody (YA8939) WB, ICC/IF, IF-Tissue, IP, ELISA human, mouse, rat

Related Diseases

Diseases Alias
Mulibrey Nanism
  • MUL

  • Muscle-Liver-Brain-Eye Nanism

  • Pericardial Constriction And Growth Failure

  • Perheentupa Syndrome

  • Mulibrey Growth Disorder

  • Mulibrey Nanism Syndrome

  • Pericardial Constriction With Growth Failure

  • Nanism Mulibrey

Acid-Labile Subunit Deficiency
  • Short Stature Due To Primary Acid-Labile Subunit Deficiency

  • ACLSD

  • Acid-Labile Subunit, Deficiency Of

  • Decreased Levels Of Acid Labile Subunit

  • Growth Disorders

Peroxisomal Disease
  • Peroxisomal Disorder

  • Peroxisomal Disorders

  • Peroxisomal Defects

Constrictive Pericarditis
  • Pericarditis, Constrictive

  • Pericarditis Constrictive

  • Pericarditis Calculosa

  • Hutinel-Pick Syndrome

  • Chronic Tamponade

  • Chronic Pericardial Constriction

  • Pick Syndrome Of Heart

  • Pick Disease Of Heart

  • Concretio Cordis

  • Calcareous Pericarditis

Childhood Osteosarcoma
  • Pediatric Osteosarcoma

Three M Syndrome 1
  • 3-M Syndrome

  • Yakut Short Stature Syndrome

  • 3m Syndrome

  • Le Merrer Syndrome

  • Dolichospondylic Dysplasia

  • Gloomy Face Syndrome

  • Three M Syndrome

  • 3M1

  • 3m Syndrome 1

  • Miller-Mckusick-Malvaux Syndrome

  • 3-Msbn

  • Three-M Slender-Boned Nanism

  • Miller-Mckusick-Malvaux-Syndrome

  • 3-M Syndrome 1

  • 3m Syndrome-1

  • 3m Syndrome, Type 1

  • Dwarfism

  • Dwarfism Tall Vertebrae

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Peroxisomal Biogenesis Disorder
  • Zellweger Spectrum Disorders

  • Peroxisome Biogenesis Disorder-Zellweger Syndrome Spectrum

  • Disorders Of Peroxisome Biogenesis

  • Zellweger Spectrum

  • Zellweger Syndrome Spectrum

  • Peroxisomal Biogenesis Disorders

  • Pbd, Zss

  • Pbd-Zsd

  • Pbd-Zss

  • Pbd-Zellweger Spectrum Disorder

  • Peroxisomal Biogenesis Disorders, Zellweger Syndrome Spectrum

  • Peroxisome Biogenesis Disorder

  • Peroxisome Biogenesis Disorder Spectrum

  • Peroxisome Biogenesis Disorders

  • Zellweger Spectrum Disorder

  • Hyperpipecolic Acidaemia

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
Rattus norvegicus TRIM37 RGD RGD:1308349
Bos taurus TRIM37 VGNC VGNC:36332
Mus musculus TRIM37 MGD MGI:2153072
Macaca mulatta TRIM37 VGNC VGNC:79966
Felis catus TRIM37 VGNC VGNC:68360
Canis familiaris TRIM37 VGNC VGNC:47818
Others TRIM37 NCBI