TRIM10: Tripartite Motif Containing 10

A RING-type E3 ubiquitin ligase involved in immune regulation and hematopoiesis.

Gene Information Card

Symbol TRIM10
Full Name Tripartite Motif Containing 10
Gene Type Protein coding
Chromosomal Location 6p21.3 (MHC class I region)
NCBI Gene ID 10107 ncbi.nlm.nih.gov/gene/10107
Ensembl ID ENSG00000132122
UniProt ID Q9UK18
OMIM ID 605701
HGNC ID 12307
Aliases RFB30, HERF1, RNF9

Description

TRIM10 (Tripartite Motif Containing 10) is a protein-coding gene located in the major histocompatibility complex (MHC) class I region on chromosome 6p21.3. It encodes a member of the tripartite motif (TRIM) family, characterized by a RING finger domain, B-box zinc fingers, and a coiled-coil region. TRIM10 functions as an E3 ubiquitin ligase, playing roles in innate immunity, hematopoietic differentiation, and protein ubiquitination. Alternative splicing generates multiple transcript variants.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hereditary Hemochromatosis (modifier) TRIM10 variants may influence iron metabolism through MHC-linked loci; exact mechanism unclear. PMID: 15654339
Autoimmune diseases (e.g., rheumatoid arthritis) Located in MHC region; polymorphisms associated with susceptibility. GWAS catalog (NHGRI-EBI)
Cancer (hematologic malignancies) Dysregulation of TRIM10 expression observed in leukemia; potential role in cell differentiation. COSMIC v99

Expression Profile

Tissue Expression
Tissue nTPM level
Bone marrow 12.5 Medium
Spleen 8.3 Low
Lymph node 6.1 Low
Testis 4.7 Low
Lung 2.1 Not detected
Cell Line Expression
Cell Line nTPM Notes
K-562 (leukemia) 15.2 Highest expression among cancer lines
HL-60 (promyeloblast) 10.8 High
HeLa (cervical) 1.5 Low
A549 (lung) 0.9 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.472C>T (p.Arg158Cys) Missense <0.01% (gnomAD) Unknown; located in B-box domain
c.1018G>A (p.Gly340Ser) Missense 0.02% (gnomAD) Unknown; located in coiled-coil region
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function variants reported in ClinVar.

Gain of Function (GOF)

Not described.

Dominant Negative (DN)

Not described.

Pathways

• Ubiquitin mediated proteolysis (KEGG: hsa04120)
• Innate immune system (Reactome: R-HSA-168249)

Protein Summary

TRIM10 is a 541-amino acid protein with a molecular weight of approximately 61 kDa. It contains an N-terminal RING finger domain (required for E3 ligase activity), two B-box zinc fingers, and a coiled-coil region. The protein localizes to the cytoplasm and nucleus. TRIM10 mediates ubiquitination of target proteins, influencing cell proliferation and differentiation, particularly in hematopoietic lineages.

Related Products

Product name Cat.No. Species Gene ID
TRIM10 Knockout HEK293 Cell Line EDJ-KQ6899 Human 10107 Details Get a Quote
TRIM10 Knockout HCT 116 Cell Line EDJ-KQ31518 Human 10107 Details Get a Quote
TRIM10 Knockout HeLa Cell Line EDJ-KQ55319 Human 10107 Details Get a Quote
TRIM10 Knockout A-549 Cell Line EDJ-KQ63803 Human 10107 Details Get a Quote
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