1. Gene
  2. TRIM38 - tripartite motif containing 38 Gene

TRIM38 - tripartite motif containing 38 Gene

Homo sapiens

Also known as RNF15; RORET

Gene ID: 10475 | Gene type: protein coding

About TRIM38

This gene has 1 transcript (splice variant), 103 orthologues and 80 paralogues. Ubiquitous expression in spleen (RPKM 9.0), lymph node (RPKM 8.4) and 24 other tissues.

Summary

This gene encodes a member of the tripartite motif (TRIM) family. The encoded protein contains a RING-type zinc finger, B box-type zinc finger and SPRY domain. The function of this protein has not been identified. A pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Jul 2012]

TRIM38 Products(1)

mRNA Protein Name
NM_006355.5 NP_006346.1 E3 ubiquitin-protein ligase TRIM38
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
23275563 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
23077300 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

TRIM38 Protein Structure

zf-C3HC4_4

zf-C3HC4_4: zinc finger of C3HC4-type, RING (16 - 62)

zf-B_box

zf-B_box: B-box zinc finger (89 - 127)

PRY

PRY: SPRY-associated domain (294 - 342)

SPRY

SPRY: SPRY domain (344 - 452)

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

E3 ubiquitin-protein ligase TRIM38

RING-type E3 ubiquitin transferase TRIM38

TRIM38 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TRIM38 O00635 FLJ13057 Homo sapiens Q53SE7 25416956
Intra
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 32296183
Intra
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 25416956
Intra
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 32296183
Intra
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 25416956
Intra
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 32296183
Intra
TRIM38 O00635 GC20 Homo sapiens Q6FG85 25416956
Intra
TRIM38 O00635 GC20 Homo sapiens Q6FG85 25416956
Intra
TRIM38 O00635 GC20 Homo sapiens Q6FG85 25416956
Intra
TRIM38 O00635 MTURN Homo sapiens Q8N3F0 32296183
Intra
TRIM38 O00635 RNF4 Homo sapiens P78317 32296183
Intra
TRIM38 O00635 RNF4 Homo sapiens P78317 32296183
Intra
TRIM38 O00635 RNF4 Homo sapiens P78317 32296183
Intra
TRIM38 O00635 TSPYL4 Homo sapiens Q9UJ04 32296183
Intra
TRIM38 O00635 HSPA8 Homo sapiens P11142 32296183
Intra
TRIM38 O00635 HSPA8 Homo sapiens P11142 25416956
Intra
TRIM38 O00635 HSPA1L Homo sapiens P34931 32296183
Intra
TRIM38 O00635 HSPA2 Homo sapiens P54652 25416956
Intra
TRIM38 O00635 HSPA2 Homo sapiens P54652 31515488
Intra
TRIM38 O00635 HSPA2 Homo sapiens P54652 25416956
Intra
TRIM38 O00635 BYSL Homo sapiens Q13895 32296183
Intra
TRIM38 O00635 PSMA4 Homo sapiens P25789 32296183
Intra
TRIM38 O00635 PSMA4 Homo sapiens P25789 32296183
Intra
TRIM38 O00635 PIAS4 Homo sapiens Q8N2W9 32296183
Intra
TRIM38 O00635 PIAS4 Homo sapiens Q8N2W9 32296183
Intra
TRIM38 O00635 PIAS4 Homo sapiens Q8N2W9 32296183
Intra
TRIM38 O00635 TCEA2 Homo sapiens Q15560 32296183
Intra
TRIM38 O00635 RFC5 Homo sapiens P40937 25416956
Intra
TRIM38 O00635 RFC5 Homo sapiens P40937 32296183
Intra
TRIM38 O00635 RFC5 Homo sapiens P40937 25416956
Intra
TRIM38 O00635 RFC5 Homo sapiens P40937 25416956
Intra
TRIM38 O00635 RFC5 Homo sapiens P40937 29892012
Intra
TRIM38 O00635 RFC5 Homo sapiens P40937 31515488
Intra
TRIM38 O00635 SDCBP Homo sapiens O00560 25416956
Intra
TRIM38 O00635 SDCBP Homo sapiens O00560 25416956
Intra
TRIM38 O00635 GORASP2 Homo sapiens Q9H8Y8 25416956
Intra
TRIM38 O00635 GORASP2 Homo sapiens Q9H8Y8 32296183
Intra
TRIM38 O00635 ZNF764 Homo sapiens Q96H86 32296183
Intra
TRIM38 O00635 ATXN1 Homo sapiens P54253 23275563
Intra
TRIM38 O00635 ATXN1 Homo sapiens P54253 32814053
Intra
TRIM38 O00635 ATXN1 Homo sapiens P54253 32814053
Intra
TRIM38 O00635 ATXN1 Homo sapiens P54253 32814053
Intra
TRIM38 O00635 STXBP1 Homo sapiens P61764 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Fanconi Renotubular Syndrome 2

FRTS2

Fanconi Renotubular Syndrome, Type 2

Acute Promyelocytic Leukemia

Leukemia, Acute Promyelocytic

Acute Myeloblastic Leukemia Type 3

Aml M3

APL

Leukemia, Acute Promyelocytic, Somatic

Aml With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Apml

Acute Myeloblastic Leukemia 3

Acute Myeloid Leukemia With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Acute Myeloblastic Leukaemia Type 3

Acute Myeloid Leukaemia M3

Acute Myeloid Leukemia M3

Acute Promyelocytic Leukaemia

M3 Anll

Myeloid Leukemia, Acute, M3

Leukemia Promyelocytic Acute

Leukemia, Promyelocytic, Acute

Leukemia, Acute, Promyelocytic

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 TRIM38 VGNC VGNC:78548
Bos taurus TRIM38 VGNC VGNC:36333
Rattus norvegicus TRIM38 RGD RGD:1596868
Canis familiaris TRIM38 VGNC VGNC:47819
Felis catus TRIM38 VGNC VGNC:66537
Mus musculus TRIM38 MGD MGI:2684869