2. Gene
  3. TRIM32 - tripartite motif containing 32 Gene

TRIM32 - tripartite motif containing 32 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as HT2A; BBS11; TATIP; LGMD2H; LGMDR8

Gene ID: 22954 | Gene type: protein coding

About TRIM32

Cytogenetic location: 9q33.1 Genomic coordinates (GRCh38): 9:116,687,305-116,701,299 (from NCBI)

This gene has 3 transcripts (splice variants), 193 orthologues, 80 paralogues and is associated with 6 phenotypes. Ubiquitous expression in endometrium (RPKM 1.6), adrenal (RPKM 1.5) and 24 other tissues.

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 localizes to cytoplasmic bodies. The protein has also been localized to the nucleus, where it interacts with the activation domain of the HIV-1 Tat protein. The Tat protein activates transcription of HIV-1 genes. [provided by RefSeq, Jul 2008]

TRIM32 Products(5)

mRNA Protein Name
NM_001099679.2 NP_001093149.1 E3 ubiquitin-protein ligase TRIM32
NM_001379048.1 NP_001365977.1 E3 ubiquitin-protein ligase TRIM32
NM_001379049.1 NP_001365978.1 E3 ubiquitin-protein ligase TRIM32
NM_001379050.1 NP_001365979.1 E3 ubiquitin-protein ligase TRIM32
NM_012210.4 NP_036342.2 E3 ubiquitin-protein ligase TRIM32
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
22493164 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables protein-macromolecule adaptor activity IDA
IDA: Inferred from direct assay
28898289 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
23077300 GOA
enables ubiquitin binding IDA
IDA: Inferred from direct assay
19349376 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
16816390 GOA
enables ubiquitin protein ligase activity IMP
IMP: Inferred from mutant phenotype
37943659 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
19349376 GOA
Biological Process GO Annotation Evidence Reference Source
involved in autophagosome assembly IDA
IDA: Inferred from direct assay
37943659 GOA
involved in cellular response to stress IDA
IDA: Inferred from direct assay
37943659 GOA
involved in free ubiquitin chain polymerization IDA
IDA: Inferred from direct assay
31123703 GOA
involved in innate immune response IDA
IDA: Inferred from direct assay
18248090 GOA
involved in negative regulation of cilium assembly IDA
IDA: Inferred from direct assay
28498859 GOA
involved in negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage IDA
IDA: Inferred from direct assay
18632609 GOA
involved in negative regulation of toll-like receptor 4 signaling pathway IDA
IDA: Inferred from direct assay
28898289 GOA
involved in negative regulation of viral transcription IDA
IDA: Inferred from direct assay
18248090 GOA
involved in positive regulation of DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
23077300 GOA
involved in positive regulation of NF-kappaB transcription factor activity IDA
IDA: Inferred from direct assay
23077300 GOA
involved in positive regulation of autophagosome assembly IDA
IDA: Inferred from direct assay
37943659 GOA
involved in positive regulation of autophagy IDA
IDA: Inferred from direct assay
31123703 GOA
involved in positive regulation of canonical NF-kappaB signal transduction IDA
IDA: Inferred from direct assay
23077300 GOA
involved in positive regulation of cell cycle IDA
IDA: Inferred from direct assay
18632609 GOA
involved in positive regulation of cell growth IDA
IDA: Inferred from direct assay
18632609 GOA
involved in positive regulation of cell migration IDA
IDA: Inferred from direct assay
18632609 GOA
involved in positive regulation of proteolysis IDA
IDA: Inferred from direct assay
18632609 GOA
involved in protein K63-linked ubiquitination IDA
IDA: Inferred from direct assay
37943659 GOA
involved in protein polyubiquitination IDA
IDA: Inferred from direct assay
18632609 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
16816390 GOA
involved in response to oxidative stress IDA
IDA: Inferred from direct assay
37943659 GOA
involved in response to starvation IDA
IDA: Inferred from direct assay
37943659 GOA
involved in suppression of viral release by host IDA
IDA: Inferred from direct assay
18248090 GOA
involved in ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
19349376 GOA
Cellular Component GO Annotation Evidence Reference Source
is active in autophagosome IDA
IDA: Inferred from direct assay
37943659 GOA
is active in centrosome IDA
IDA: Inferred from direct assay
28498859 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
19349376 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TRIM32 Protein Structure

zf-RING_UBOX

zf-RING_UBOX: RING-type zinc-finger (20 - 62)

NHL

NHL: NHL repeat (371 - 398)

NHL

NHL: NHL repeat (469 - 496)

NHL

NHL: NHL repeat (616 - 643)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 600
  • 653 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase TRIM32

72 kDa Tat-interacting protein

TRIM32 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0-2
Validated Y2H
25416956
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0-2
Y2H Array
25416956
Intra
TRIM32 Q13049 b3kpu6_human Homo sapiens B3KPU6
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 b3kpu6_human Homo sapiens B3KPU6
Y2H Array
25416956
Intra
TRIM32 Q13049 SYT6 Homo sapiens Q5T7P8-2
Validated Y2H
25416956
Intra
TRIM32 Q13049 SYT6 Homo sapiens Q5T7P8-2
Validated Y2H
32296183
Intra
TRIM32 Q13049 SYT6 Homo sapiens Q5T7P8-2
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 UBE2V1 Homo sapiens Q13404
Validated Y2H
32296183
Intra
TRIM32 Q13049 UBE2N Homo sapiens P61088
Y2H Array
19549727
Intra
TRIM32 Q13049 UBE2N Homo sapiens P61088
Y2H Array
19690564
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
Y2H Array
32296183
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
SLC
25910212
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
Validated Y2H
25910212
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
Y2H Array
25910212
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
Validated Y2H
32296183
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9-2
Y2H Bait-Prey Pool
25910212
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-2
Y2H Array
32296183
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-2
SLC
25910212
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-2
Validated Y2H
25910212
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-2
Y2H Bait-Prey Pool
25910212
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-2
Y2H Array
25910212
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-2
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 TCEANC Homo sapiens Q8N8B7-2
Validated Y2H
32296183
Intra
TRIM32 Q13049 PTCD2 Homo sapiens Q8WV60
Validated Y2H
32296183
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083-4
Y2H Array
26871637
Intra
TRIM32 Q13049 SEC23IP Homo sapiens Q9Y6Y8
Anti Tag CoIP
33961781
Intra
TRIM32 Q13049 SEC23IP Homo sapiens Q9Y6Y8
TAP
27173435
Intra
TRIM32 Q13049 GPR137B Homo sapiens O60478
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 GPR137B Homo sapiens O60478
Y2H Array
32296183
Intra
TRIM32 Q13049 UBE2U Homo sapiens Q5VVX9
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 UBE2U Homo sapiens Q5VVX9
Y2H Array
19549727
Intra
TRIM32 Q13049 UBE2U Homo sapiens Q5VVX9
Validated Y2H
25416956
Intra
TRIM32 Q13049 PTPN11 Homo sapiens Q06124
Y2H Pooling
27229929
Intra
TRIM32 Q13049 FADS6 Homo sapiens Q8N9I5
Validated Y2H
32296183
Intra
TRIM32 Q13049 FADS6 Homo sapiens Q8N9I5
Y2H Array
32296183
Intra
TRIM32 Q13049 FADS6 Homo sapiens Q8N9I5
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 DERL1 Homo sapiens Q9BUN8
Y2H Array
32296183
Intra
TRIM32 Q13049 DERL1 Homo sapiens Q9BUN8
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 DERL1 Homo sapiens Q9BUN8
Validated Y2H
32296183
Intra
TRIM32 Q13049 KCTD9 Homo sapiens Q7L273
Validated Y2H
32296183
Intra
TRIM32 Q13049 KCTD9 Homo sapiens Q7L273
Y2H Array
25416956
Intra
TRIM32 Q13049 KCTD9 Homo sapiens Q7L273
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 PELI2 Homo sapiens Q9HAT8
Validated Y2H
32296183
Intra
TRIM32 Q13049 CLIP4 Homo sapiens Q8N3C7
Validated Y2H
32296183
Intra
TRIM32 Q13049 CLIP4 Homo sapiens Q8N3C7
Y2H Array
25416956
Intra
TRIM32 Q13049 UBQLN4 Homo sapiens Q9NRR5
Pull Down
16713569
Intra
TRIM32 Q13049 UBQLN4 Homo sapiens Q9NRR5
Y2H Array
16713569
Intra
TRIM32 Q13049 AKTIP Homo sapiens Q9H8T0
Y2H Fragment Pooling
23414517
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Validated Y2H
25910212
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Y2H Bait-Prey Pool
25910212
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Y2H Array
25910212
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Validated Y2H
32296183
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
SLC
25910212
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Y2H Array
32296183
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 RABAC1 Homo sapiens Q9UI14
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 SDCBP Homo sapiens O00560
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 SDCBP Homo sapiens O00560
Validated Y2H
25416956
Intra
TRIM32 Q13049 NTAQ1 Homo sapiens Q96HA8
Validated Y2H
32296183
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Y2H Pooling
16189514
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Validated Y2H
32296183
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Y2H Array
25416956
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Y2H Array
32296183
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 UBQLN1 Homo sapiens Q9UMX0
Validated Y2H
25416956
Intra
TRIM32 Q13049 PDE9A Homo sapiens O76083
Validated Y2H
25416956
Intra
TRIM32 Q13049 SCGB1A1 Homo sapiens P11684
Y2H
21516116
Intra
TRIM32 Q13049 SCGB1A1 Homo sapiens P11684
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 SCGB1A1 Homo sapiens P11684
Validated Y2H
25416956
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9
Y2H Prey Pooling
25416956
Intra
TRIM32 Q13049 ABI2 Homo sapiens Q9NYB9
Y2H Array
29892012
Intra
TRIM32 Q13049 MOB1A Homo sapiens Q9H8S9
Validated Y2H
32296183
Intra
TRIM32 Q13049 ERGIC3 Homo sapiens Q9Y282
Validated Y2H
32296183
Intra
TRIM32 Q13049 ERGIC3 Homo sapiens Q9Y282
Y2H Array
32296183
Intra
TRIM32 Q13049 ERGIC3 Homo sapiens Q9Y282
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 TTC23 Homo sapiens Q5W5X9-3
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 TTC23 Homo sapiens Q5W5X9-3
Validated Y2H
32296183
Intra
TRIM32 Q13049 TTC23 Homo sapiens Q5W5X9-3
Y2H Array
32296183
Intra
TRIM32 Q13049 ATXN1 Homo sapiens P54253
Y2H Array
16713569
Intra
TRIM32 Q13049 UBQLN2 Homo sapiens Q9UHD9
Validated Y2H
32296183
Intra
TRIM32 Q13049 UBQLN2 Homo sapiens Q9UHD9
Y2H Prey Pooling
32296183
Intra
TRIM32 Q13049 UBQLN2 Homo sapiens Q9UHD9
Y2H Array
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8

Sarcotubular Myopathy

Lgmd2h

Muscular Dystrophy, Limb-Girdle, Type 2h

Limb-Girdle Muscular Dystrophy Type 2h

LGMDR8

Muscular Dystrophy Hutterite Type

Muscular Dystrophy, Hutterite Type

Muscular Dystrophy Limb-Girdle Type 2h

Trim32-Related Limb-Girdle Muscular Dystrophy R8

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h

Lgmd Due To Trim32 Deficiency

Lgmd Type 2h

Limb-Girdle Muscular Dystrophy Due To Trim32 Deficiency

Trim32-Related Lgmd R8

Limb-Girdle Muscular Dystrophy 2h

Dystrophy, Muscular, Limb-Girdle, Type 2h
Bardet-Biedl Syndrome 11

BBS11

Bardet-Biedl Syndrome

Bbs

Bardet-Biedl Syndrome, Type 11
Bardet-Biedl Syndrome

Bbs

Biedl-Bardet Syndrome
Isolated Elevated Serum Creatine Phosphokinase Levels

Elevated Serum Cpk

Idiopathic Hyperckemia

Isolated Hyperckemia

Elevated Serum Creatine Phosphokinase

H-Ck

Idiopathic Persistent Elevation Of Serum Creatine Kinase
Creatine Phosphokinase, Elevated Serum

Hyperckemia, Idiopathic

Cpk, Elevated Serum

Hyperckmia

HYPCK
Myopathy

Muscular Diseases

Myopathies
Limb-Girdle Muscular Dystrophy

Lgmd

Limb Girdle Muscular Dystrophy

Muscular Dystrophies, Limb-Girdle

Erb'S Muscular Dystrophy

Leyden-Mbius Muscular Dystrophy

Limb-Girdle Syndrome

Myopathic Limb-Girdle Syndrome

Limb Girdle

Muscular Dystrophy Limb-Girdle

Dystrophy, Muscular, Limb-Girdle

Lgmd - [Limb-Girdle Muscular Dystrophy]

Limb Girdle Muscle Dystrophy

Limb-Girdle Myopathy
Autosomal Recessive Limb-Girdle Muscular Dystrophy

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h

Lgmd2h

Limb-Girdle Muscular Dystrophy Due To Trim32 Deficiency

Muscular Dystrophy Hutterite Type

Sarcotubular Myopathy

Limb-Girdle Muscular Dystrophy Type 2h
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7

Muscular Dystrophy, Limb-Girdle, Type 2g

Lgmd2g

LGMDR7

Limb-Girdle Muscular Dystrophy, Type 2g

Telethonin-Related Limb-Girdle Muscular Dystrophy R7

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g

Lgmd Due To Telethonin Deficiency

Lgmd Type 2g

Limb-Girdle Muscular Dystrophy Due To Telethonin Deficiency

Limb-Girdle Muscular Dystrophy Type 2g

Telethonin-Related Lgmd R7

Limb-Girdle Muscular Dystrophy 2g

Dystrophy, Muscular, Limb-Girdle, Type 2g
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Lgmd2e

Muscular Dystrophy, Limb-Girdle, Type 2e

LGMDR4

Beta-Sarcoglycan-Related Limb-Girdle Muscular Dystrophy R4

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e

Beta-Sarcoglycan-Related Lgmd R4

Beta-Sarcoglycanopathy

Lgmd Due To Beta-Sarcoglycan Deficiency

Lgmd Type 2e

Limb-Girdle Muscular Dystrophy Due To Beta-Sarcoglycan Deficiency

Limb-Girdle Muscular Dystrophy Type 2e

Limb-Girdle Muscular Dystrophy 2e
Muscular Dystrophy

Muscular Dystrophies

Congenital Md

Congenital Muscular Dystrophy

Cmd

Mdc

Dystrophy, Muscular

Gower'S Muscular Dystrophy

Progressive Musclular Dystrophy

Pseudohypertrophic Atrophy

Pseudohypertrophic Muscle Paralysis

Pseudohypertrophic Muscular Atrophy

Pseudohypertrophic Muscular Dystrophy

Pseudohypertrophic Paralysis

Pseudomuscular Hypertrophy
Muscular Dystrophy-Dystroglycanopathy , Type C, 5

Lgmd2i

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2i

MDDGC5

Limb-Girdle Muscular Dystrophy Due To Fkrp Deficiency

Limb-Girdle Muscular Dystrophy Type 2i

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 9

Lgmdr9

Muscular Dystrophy, Limb-Girdle, Type 2i

Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Frkp-Related

Fkrp-Related Limb-Girdle Muscular Dystrophy R9

Fkrp-Related Lgmd R9

Lgmd Due To Fkrp Deficiency

Lgmd Type 2i

Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Frkp-Related

Muscular Dystrophy Limb-Girdle Type 2i

Muscular Dystrophy-Dystroglycanopathy Type C 5

Muscular Dystrophy-Dystroglycanopathy Limb-Girdle C5

Dystrophy, Muscular, Limb-Girdle, Type 2i
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6

Lgmd2f

Muscular Dystrophy, Limb-Girdle, Type 2f

Limb-Girdle Muscular Dystrophy Type 2f

LGMDR6

Muscular Dystrophy Limb-Girdle With Delta-Sarcoglyan Deficiency

Delta-Sarcoglycan-Related Limb-Girdle Muscular Dystrophy R6

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f

Delta-Sarcoglycan-Related Lgmd R6

Delta-Sarcoglycanopathy

Lgmd Due To Delta-Sarcoglycan Deficiency

Lgmd Type 2f

Limb-Girdle Muscular Dystrophy Due To Delta-Sarcoglycan Deficiency

Limb-Girdle Muscular Dystrophy 2f

Limb-Girdle Muscular Dystrophy, Type 2f

Dystrophy, Muscular, Limb-Girdle, Type 2f
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2

Lgmd2b

Muscular Dystrophy, Limb-Girdle, Type 2b

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e

Beta-Sarcoglycanopathy

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2y

Muscular Dystrophy, Limb-Girdle, Type 3

Lgmd3

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2s

LGMDR2

Muscular Dystrophy, Limb-Girdle, Type 2s

Limb-Girdle Muscular Dystrophy Type 2b

Lgmd2e

Limb-Girdle Muscular Dystrophy Due To Beta-Sarcoglycan Deficiency

Muscular Dystrophy, Limb-Girdle, Type 2e

Lgmd2s

Autosomal Recessive Muscular Dystrophy Due To Lap1b Deficiency

Autosomal Recessive Muscular Dystrophy Due To Torsin-1a-Interacting Protein 1 Deficiency

Lgmd2y

Muscular Dystrophy With Progressive Weakness, Distal Contractures And Rigid Spine

Muscular Dystrophy, Limb-Girdle, Type 2y

Dysferlin-Related Limb-Girdle Muscular Dystrophy R2

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b

Dysferlin-Related Lgmd R2

Lgmd Due To Dysferlin Deficiency

Lgmd Type 2b

Limb-Girdle Muscular Dystrophy Due To Dysferlin Deficiency

Limb-Girdle Muscular Dystrophy 2b

Limb-Girdle Muscular Dystrophy, Type 2b

Dystrophy, Muscular, Limb-Girdle, Autosomal Recessive, Type 2

Dystrophy, Muscular, Limb-Girdle, Type 2b

Limb-Girdle Muscular Dystrophy, Type 2e
Limb-Girdle Muscular Dystrophy Type 1a

Lgmd1a

Lgmd1

Muscular Dystrophy, Proximal, Type 1a

Limb-Girdle Muscular Dystrophy, Type 1a

Dystrophy, Muscular, Limb-Girdle, Type 1a
Joubert Syndrome 6

JBTS6

Joubert Syndrome, Type 6
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j

Lgmd2j

Muscular Dystrophy, Limb-Girdle, Type 2j
Polydactyly

Non-Syndromic Polydactyly

Polydactyly, Postaxial

Postaxial Polydactyly

Supernumerary Digit

Extra Digits

Hyperdactyly

Polydactylia

Polydactylism

Supernumerary Digits
Melancholia
Myopathy, Spheroid Body

Spheroid Body Myopathy

Autosomal Dominant Spheroid Body Myopathy

SBM
Mulibrey Nanism

MUL

Muscle-Liver-Brain-Eye Nanism

Pericardial Constriction And Growth Failure

Perheentupa Syndrome

Mulibrey Growth Disorder

Mulibrey Nanism Syndrome

Pericardial Constriction With Growth Failure

Nanism Mulibrey
Major Depressive Disorder

Seasonal Affective Disorder

Unipolar Depression

Depression

MDD

Depressive Disorder

Unipolar Depression, Susceptibility To

Major Depressive Disorder 1

Major Depressive Disorder, Response To Citalopram Therapy In

Major Depressive Disorder 2

Winter Depression

Single Major Depressive Episode

Sad

Clinical Depression

Major Depression

Depressive Syndrome

Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment

Seasonal Affective Disorder, Susceptibility To

Recurrent Major Depression

Affective Disorder, Seasonal

Depression In A Seasonal Pattern

Depression

Seasonal

Major Depressive Disorder With A Seasonal Pattern

Seasonal Depression

Seasonal Mood Disorder

Mental Depression

Recurrent Major Depressive Episodes
Myoclonic Epilepsy Of Lafora

Lafora Disease

Epilepsy, Progressive Myoclonic 2b

EPM2

Melf

Epilepsy, Progressive Myoclonic 2a

Epm2a

Lafora'S Disease

Lafora Body Disease

Lbd

Epilepsy, Progressive Myoclonic, 2a

Lafora Progressive Myoclonic Epilepsy

Epilepsy Progressive Myoclonic 2

Lafora Body Disorder

Pme Type 2

Progressive Myoclonic Epilepsy Type 2

Progressive Myoclonus Epilepsy Type 2

Epilepsy, Progressive Myoclonic 2

Epm2b

Ld

Progressive Myoclonic Epilepsy 2

Progressive Myoclonic Epilepsy 2a

Progressive Myoclonic Epilepsy 2b

Progressive Myoclonic Epilepsy Lafora Type

Epilepsy, Myoclonic, Of Lafora
Heart Disease

Heart Failure

Congenital Heart Disease

Heart Diseases

Congenital Heart Defects

Congenital Heart Defect

Heart Malformation

Congenital Anomaly Of Heart

Heart Defect

Heart-Congenital Defect

Congenital Heart Disorder

Heart Defects Congenital

Heart Defects, Congenital

Heart Defects

Heart Disease, Congenital

Disease, Heart, Congenital

Congestive Heart Failure
Psychotic Disorder

Psychotic Disorders

Mental Or Behavioural Disorder

Psychotic

Mental Disorders
Myofibrillar Myopathy

Desmin Related Myopathy

Myotilinopathy

Myopathy, Myofibrillar

Alpha Beta Crystallinopathy

Desmin Storage Myopathy

Desminopathy

Filaminopathy

Protein Surplus Myopathy

Zaspopathy

Myofibrillar Myopathies

Myopathy, Myofibrillar, Desmin-Related

Myopathy, Desmin Storage

Mfm - [Myofibrillar Myopathy]
Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic
Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal
Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS15037 TRIM32 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus TRIM32 VGNC VGNC:36328
Felis catus TRIM32 VGNC VGNC:66534
Canis familiaris TRIM32 VGNC VGNC:47814
Rattus norvegicus TRIM32 RGD RGD:1305238
Mus musculus TRIM32 MGD MGI:1917057
Macaca mulatta TRIM32 VGNC VGNC:79032
Others TRIM32 NCBI