TRIM36: Tripartite Motif Containing 36

A RING-type E3 ubiquitin ligase involved in cell cycle regulation and neurodevelopment

Gene Information Card

Symbol TRIM36
Full Name Tripartite Motif Containing 36
Gene Type Protein coding
Chromosomal Location 5q22.3
NCBI Gene ID 57121 ncbi.nlm.nih.gov/gene/57121
Ensembl ID ENSG00000113555
UniProt ID Q9H6V9
OMIM ID 607215
HGNC ID 16280
Aliases RNF98, HAPRIN, RBCC728

Description

TRIM36 (Tripartite Motif Containing 36) encodes a member of the tripartite motif (TRIM) family, characterized by a RING finger domain, B-box zinc finger, and coiled-coil region. The protein functions as an E3 ubiquitin ligase, mediating ubiquitination and proteasomal degradation of target proteins. TRIM36 is involved in cell cycle regulation, microtubule stabilization, and neurodevelopment. It is expressed in multiple tissues, with highest levels in testis and brain. Mutations and altered expression have been associated with cancer and neurological disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Prostate cancer TRIM36 overexpression may promote tumor growth via ubiquitination of cell cycle regulators COSMIC; PMID: 25691885
Gastric cancer Downregulation of TRIM36 correlates with poor prognosis; potential tumor suppressor NCBI Gene; PMID: 29367642
Neurodevelopmental disorders Missense variants in TRIM36 associated with intellectual disability and autism spectrum disorder ClinVar; PMID: 31036916

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 48.2 High
Brain 12.5 Medium
Lung 6.8 Low
Liver 3.1 Low
Heart 2.4 Low
Cell Line Expression
Cell Line nTPM Notes
HEK293 15.3 Embryonic kidney cells
HeLa 8.7 Cervical cancer cells
MCF7 5.2 Breast cancer cells
A549 4.1 Lung cancer cells
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1045C>T (p.Arg349Trp) Missense 0.001% Unknown; reported in ClinVar as variant of uncertain significance
c.1573G>A (p.Glu525Lys) Missense 0.002% Unknown; associated with neurodevelopmental phenotypes
c.1882_1883del (p.Leu628ValfsTer2) Frameshift 0.0005% Loss of function; predicted to cause protein truncation
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations predicted to cause protein truncation or nonsense-mediated decay, leading to loss of E3 ubiquitin ligase activity.

Gain of Function (GOF)

Not well characterized; some missense variants may alter substrate specificity or increase ubiquitination activity.

Dominant Negative (DN)

Not reported for TRIM36.

Pathways

• Ubiquitin mediated proteolysis (KEGG: hsa04120)
• Cell cycle (Reactome: R-HSA-1640170)

Protein Summary

TRIM36 is a 728-amino acid protein with a molecular weight of approximately 82 kDa. It contains an N-terminal RING finger domain (E3 ubiquitin ligase activity), two B-box zinc fingers, a coiled-coil region, and a C-terminal SPRY domain. The protein localizes to the cytoplasm and centrosome, where it regulates microtubule dynamics and cell cycle progression. TRIM36 ubiquitinates target proteins such as cyclins and spindle-associated factors, targeting them for proteasomal degradation. Its expression is enriched in testis and brain, suggesting roles in spermatogenesis and neuronal development.

Related Products

Product name Cat.No. Species Gene ID
TRIM36 Knockout HEK293 Cell Line EDJ-KQ15916 Human 55521 Details Get a Quote
TRIM36 Knockout A-549 Cell Line EDJ-KQ46922 Human 55521 Details Get a Quote
TRIM36 Knockout HCT 116 Cell Line EDJ-KQ46923 Human 55521 Details Get a Quote
TRIM36 Knockout HeLa Cell Line EDJ-KQ46924 Human 55521 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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