TRIM36
E3 ubiquitin-protein ligase TRIM36
Also known as: HAPRIN, RBCC728, RNF98, TRI36_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NQ86
- Gene
- TRIM36
- Ensembl
- ENSG00000152503
- Chromosome
- 5
- Canonical length
- 728 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
728 residues, UniProt reviewed canonical sequence.
>Q9NQ86|TRIM36
1 MSESGEMSEF GYIMELIAKG KVTIKNIERE LICPACKELF THPLILPCQH SICHKCVKEL
61 LLTLDDSFND VGSDNSNQSS PRLRLPSPSM DKIDRINRPG WKRNSLTPRT TVFPCPGCEH
121 DVDLGERGIN GLFRNFTLET IVERYRQAAR AATAIMCDLC KPPPQESTKS CMDCSASYCN
181 ECFKIHHPWG TIKAQHEYVG PTTNFRPKIL MCPEHETERI NMYCELCRRP VCHLCKLGGN
241 HANHRVTTMS SAYKTLKEKL SKDIDYLIGK ESQVKSQISE LNLLMKETEC NGERAKEEAI
301 THFEKLFEVL EERKSSVLKA IDSSKKLRLD KFQTQMEEYQ GLLENNGLVG YAQEVLKETD
361 QSCFVQTAKQ LHLRIQKATE SLKSFRPAAQ TSFEDYVVNT SKQTELLGEL SFFSSGIDVP
421 EINEEQSKVY NNALINWHHP EKDKADSYVL EYRKINRDDE MSWNEIEVCG TSKIIQDLEN
481 SSTYAFRVRA YKGSICSPCS RELILHTPPA PVFSFLFDEK CGYNNEHLLL NLKRDRVESR
541 AGFNLLLAAE RIQVGYYTSL DYIIGDTGIT KGKHFWAFRV EPYSYLVKVG VASSDKLQEW
601 LRSPRDAVSP RYEQDSGHDS GSEDACFDSS QPFTLVTIGM QKFFIPKSPT SSNEPENRVL
661 PMPTSIGIFL DCDKGKVDFY DMDQMKCLYE RQVDCSHTLY PAFALMGSGG IQLEEPITAK
721 YLEYQEDMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRIM36 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 163 nTPM
Expression across tissuesHPA
Tissue
- testis: 163 nTPM
- retina: 41 nTPM
- spinal cord: 17 nTPM
- cerebral cortex: 15 nTPM
- blood vessel: 14 nTPM
- choroid plexus: 14 nTPM
Single-cell type
- late spermatids: 7,747 nCPM
- early spermatids: 2,529 nCPM
- late primary spermatocytes: 697 nCPM
- rod photoreceptor cells: 174 nCPM
- thyrotrophs: 160 nCPM
- pituitary stem cells: 150 nCPM
Immune cell
- non-classical monocyte: 6.5 nTPM
- myeloid DC: 5.8 nTPM
- eosinophil: 3.2 nTPM
- intermediate monocyte: 1.3 nTPM
- classical monocyte: 1.2 nTPM
- plasmacytoid DC: 1.2 nTPM
Brain region
- white matter: 51 nTPM
- medulla oblongata: 44 nTPM
- pons: 42 nTPM
- basal ganglia: 42 nTPM
- hippocampal formation: 42 nTPM
- hypothalamus: 42 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TRIM36.
Disease | AllUniProt
Conditions TRIM36 is implicated in, by any mechanism.
- Anencephaly 1 (ANPH1) MIM:206500
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 127 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.66
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.4
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- acrosome reaction
- mitotic cytokinesis
- regulation of cell cycle
- regulation of microtubule cytoskeleton organization
- spindle organization
Molecular functions
- alpha-tubulin binding
- ubiquitin protein ligase activity
- ubiquitin-protein transferase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- B-box-type zinc finger
- Zinc finger, RING-type
- B30.2/SPRY domain
- Butyrophylin-like, SPRY domain
- Fibronectin type III
- Zinc finger, RING/FYVE/PHD-type
- Concanavalin A-like lectin/glucanase domain superfamily
- Immunoglobulin-like fold
- COS domain
- Zinc finger, RING-type, conserved site
- Zinc finger, RING-type, eukaryotic
- Fibronectin type III superfamily
- Midline-1, COS domain
- B30.2/SPRY domain superfamily
- E3 ubiquitin-protein ligases and FN3/SPRY domain-containing proteins
- Fibronectin type III domain
- B-box zinc finger
- RING-type zinc-finger
- TRIM C-terminal subgroup One Signature domain
- ANCHR-like B-box zinc-binding domain
- E3 ubiquitin-protein ligase Trim36, RING finger, HC subclass
- TRIM36, PRY/SPRY domain
- E3 ubiquitin-protein ligase Trim36, B-box-type 2 zinc finger
- E3 ubiquitin-protein ligase Trim36, B-box-type 1 zinc finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRIM36 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TRIM36 as an antibody target. Whether an autoantibody or antibody against TRIM36 could matter depends on whether native TRIM36 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRIM36 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TRIM36 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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