Gene Gene information from NCBI Gene database.
Entrez ID 85363
Gene name Tripartite motif containing 5
Gene symbol TRIM5
Synonyms (NCBI Gene)
RNF88TRIM5alpha
Chromosome 11
Chromosome location 11p15.4
Summary 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. The protein forms homo-oligomers via the coilel-co
miRNA miRNA information provided by mirtarbase database.
257
miRTarBase ID miRNA Experiments Reference
MIRT052397 hsa-let-7a-5p CLASH 23622248
MIRT449416 hsa-miR-548u PAR-CLIP 22100165
MIRT449414 hsa-miR-7161-5p PAR-CLIP 22100165
MIRT449415 hsa-miR-8087 PAR-CLIP 22100165
MIRT449413 hsa-miR-4712-3p PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
49
GO ID Ontology Definition Evidence Reference
GO:0000932 Component P-body IDA 12878161, 20357094
GO:0002218 Process Activation of innate immune response IDA 21512573
GO:0002376 Process Immune system process IEA
GO:0003713 Function Transcription coactivator activity IDA 23077300
GO:0004842 Function Ubiquitin-protein transferase activity IDA 21512573
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608487 16276 ENSG00000132256
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9C035
Protein name Tripartite motif-containing protein 5 (EC 2.3.2.27) (RING finger protein 88) (RING-type E3 ubiquitin transferase TRIM5)
Protein function Capsid-specific restriction factor that prevents infection from non-host-adapted retroviruses. Blocks viral replication early in the life cycle, after viral entry but before reverse transcription. In addition to acting as a capsid-specific restr
PDB 2ECV , 2YRG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13445 zf-RING_UBOX 15 56 RING-type zinc-finger Domain
PF00643 zf-B_box 90 131 B-box zinc finger Domain
PF00622 SPRY 358 489 SPRY domain Family
Sequence
MASGILVNVKEEVTCPICLELLTQPLSLDCGHSFCQACLTANHKKSMLDKGESSCPVCRI
SYQPENIRPNRHVANIVEKLREVKLSPEGQKVDHCARHGEKLLLFCQEDGKVICWLCERS
QEHRGHHTFLT
EEVAREYQVKLQAALEMLRQKQQEAEELEADIREEKASWKTQIQYDKTN
VLADFEQLRDILDWEESNELQNLEKEEEDILKSLTNSETEMVQQTQSLRELISDLEHRLQ
GSVMELLQGVDGVIKRTENVTLKKPETFPKNQRRVFRAPDLKGMLEVFRELTDVRRYWVD
VTVAPNNISCAVISEDKRQVSSPKPQIIYGARGTRYQTFVNFNYCTGILGSQSITSGKHY
WEVDVSKKTAWILGVCAGFQPDAMCNIEKNENYQPKYGYWVIGLEEGVKCSAFQDSSFHT
PSVPFIVPLSVIICPDRVGVFLDYEACTVSFFNITNHGFLIYKFSHCSFSQPVFPYLNPR
KCGVPMTLC
SPSS
Sequence length 493
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Viral life cycle - HIV-1
Human immunodeficiency virus 1 infection
  Interferon gamma signaling
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEAD AND NECK MALIGNANT NEOPLASIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INTRACEREBRAL HEMORRHAGE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MYOCARDIAL INFARCTION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Autoimmune Diseases Autoimmune Diseases BEFREE 31312031
★☆☆☆☆
Found in Text Mining only
Behcet Syndrome Behcet disease Pubtator 37264476 Associate
★☆☆☆☆
Found in Text Mining only
Coronary Artery Disease Coronary artery disease GWASCAT_DG 29212778
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Fibrosis, Liver Liver Fibrosis BEFREE 27590274
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 37367937 Stimulate
★☆☆☆☆
Found in Text Mining only
Hepatitis B Hepatitis b Pubtator 27590274 Associate
★☆☆☆☆
Found in Text Mining only
Immunologic Deficiency Syndromes Immunologic Deficiency Syndromes BEFREE 15709033, 16809279, 16840314, 20107597, 21734037, 22124667
★☆☆☆☆
Found in Text Mining only
leukemia Leukemia BEFREE 15249685, 16699044, 16887163, 17400754
★☆☆☆☆
Found in Text Mining only
leukemia Leukemia LHGDN 15249690, 15767395, 18166079
★☆☆☆☆
Found in Text Mining only
Liver Cirrhosis Liver cirrhosis Pubtator 27590274 Associate
★☆☆☆☆
Found in Text Mining only