Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
22954
Gene name Gene Name - the full gene name approved by the HGNC.
Tripartite motif containing 32
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRIM32
Synonyms (NCBI Gene) Gene synonyms aliases
BBS11, HT2A, LGMD2H, LGMDR8, TATIP
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q33.1
Summary Summary of gene provided in NCBI Entrez 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. The protein localizes to cytoplasmic bodies. The p
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT001492 hsa-miR-155-5p pSILAC 18668040
MIRT001492 hsa-miR-155-5p Proteomics;Other 18668040
MIRT031385 hsa-miR-16-5p Proteomics 18668040
MIRT001492 hsa-miR-155-5p Microarray, qRT-PCR 25128227
MIRT001492 hsa-miR-155-5p Microarray, qRT-PCR 25128227
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000045 Process Autophagosome assembly IDA 37943659
GO:0000045 Process Autophagosome assembly IDA 37943659
GO:0000045 Process Autophagosome assembly IMP 22170151
GO:0000209 Process Protein polyubiquitination IDA 18632609
GO:0000209 Process Protein polyubiquitination IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602290 16380 ENSG00000119401
Protein
UniProt ID Q13049
Protein name E3 ubiquitin-protein ligase TRIM32 (EC 2.3.2.27) (72 kDa Tat-interacting protein) (RING-type E3 ubiquitin transferase TRIM32) (Tripartite motif-containing protein 32) (Zinc finger protein HT2A)
Protein function E3 ubiquitin ligase that plays a role in various biological processes including neural stem cell differentiation, innate immunity, inflammatory resonse and autophagy (PubMed:19349376, PubMed:31123703). Plays a role in virus-triggered induction o
PDB 2CT2 , 5FEY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13445 zf-RING_UBOX 20 62 RING-type zinc-finger Domain
PF01436 NHL 371 398 NHL repeat Repeat
PF01436 NHL 469 496 NHL repeat Repeat
PF01436 NHL 616 643 NHL repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Spleen, thymus, prostate, testis, ovary, intestine, colon and skeletal muscle. {ECO:0000269|PubMed:11822024}.
Sequence
MAAAAASHLNLDALREVLECPICMESFTEEQLRPKLLHCGHTICRQCLEKLLASSINGVR
CP
FCSKITRITSLTQLTDNLTVLKIIDTAGLSEAVGLLMCRSCGRRLPRQFCRSCGLVLC
EPCREADHQPPGHCTLPVKEAAEERRRDFGEKLTRLRELMGELQRRKAALEGVSKDLQAR
YKAVLQEYGHEERRVQDELARSRKFFTGSLAEVEKSNSQVVEEQSYLLNIAEVQAVSRCD
YFLAKIKQADVALLEETADEEEPELTASLPRELTLQDVELLKVGHVGPLQIGQAVKKPRT
VNVEDSWAMEATASAASTSVTFREMDMSPEEVVASPRASPAKQRGPEAASNIQQCLFLKK
MGAKGSTPGMFNLPVSLYVTSQGEVLVADRGNYRIQVFTRKGFLKEIRRSPSGIDSFVLS
FLGADLPNLTPLSVAMNCQGLIGVTDSYDNSLKVYTLDGHCVACHRSQLSKPWGITALPS
GQFVVTDVEGGKLWCF
TVDRGSGVVKYSCLCSAVRPKFVTCDAEGTVYFTQGLGLNLENR
QNEHHLEGGFSIGSVGPDGQLGRQISHFFSENEDFRCIAGMCVDARGDLIVADSSRKEIL
HFPKGGGYSVLIREGLTCPVGIALTPKGQLLVLDCWDHCIKIYSYHLRRYSTP
Sequence length 653
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Ubiquitin mediated proteolysis   Regulation of innate immune responses to cytosolic DNA
Antigen processing: Ubiquitination & Proteasome degradation
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Bardet-Biedl Syndrome bardet-biedl syndrome, bardet-biedl syndrome 11 rs1588218453, rs886044106, rs759376012, rs111033570, rs747685252, rs1564218190, rs111033571, rs747266069, rs398124253, rs35904234 N/A
Limb-girdle muscular dystrophy Limb-girdle muscular dystrophy rs747685252 N/A
retinal dystrophy Retinal dystrophy rs111033570 N/A
sarcotubular myopathy Sarcotubular myopathy rs111033570, rs747266069, rs1588218453 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Muscular dystrophy autosomal recessive limb-girdle muscular dystrophy N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Amyotrophic Lateral Sclerosis Associate 23469062
Arthritis Rheumatoid Associate 32145086
Atrophy Associate 31234693
Attention Deficit Disorder with Hyperactivity Associate 24381304
Autism Spectrum Disorder Associate 24381304
Bardet Biedl Syndrome Associate 20177705, 23404957, 25351777, 30823891
Carcinogenesis Associate 21628460
Carcinoma Renal Cell Associate 33173411
Cognition Disorders Associate 25351777
Developmental Disabilities Associate 24381304