1. Gene
  2. TRIM21 - tripartite motif containing 21 Gene

TRIM21 - tripartite motif containing 21 Gene

Homo sapiens

Also known as SSA; RO52; SSA1; RNF81; Ro/SSA

Gene ID: 6737 | Gene type: protein coding

About TRIM21

Cytogenetic location: 11p15.4 Genomic coordinates (GRCh38): 11:4,384,897-4,393,702 (from NCBI)

This gene has 2 transcripts (splice variants), 96 orthologues and 80 paralogues. Ubiquitous expression in spleen (RPKM 15.5), appendix (RPKM 13.2) and 24 other tissues.

Summary

This gene encodes 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 encoded protein is part of the RoSSA ribonucleoprotein, which includes a single polypeptide and one of four small RNA molecules. The RoSSA particle localizes to both the cytoplasm and the nucleus. RoSSA interacts with autoantigens in patients with Sjogren syndrome and systemic lupus erythematosus. Alternatively spliced transcript variants for this gene have been described but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]

TRIM21 Products(1)

mRNA Protein Name
NM_003141.4 NP_003132.2 E3 ubiquitin-protein ligase TRIM21
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
17156811 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8666824 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
23077300 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
26342464 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
16297862 GOA
Biological Process GO Annotation Evidence Reference Source
involved in innate immune response IDA
IDA: Inferred from direct assay
18248090 GOA
involved in negative regulation of NF-kappaB transcription factor activity IDA
IDA: Inferred from direct assay
19675099 GOA
involved in negative regulation of innate immune response IDA
IDA: Inferred from direct assay
26342464 GOA
involved in negative regulation of protein deubiquitination IMP
IMP: Inferred from mutant phenotype
16472766 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 autophagy IMP
IMP: Inferred from mutant phenotype
26347139 GOA
involved in positive regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
16880511 GOA
involved in positive regulation of protein binding IMP
IMP: Inferred from mutant phenotype
26342464 GOA
involved in proteasomal protein catabolic process IDA
IDA: Inferred from direct assay
36359729 GOA
involved in protein K27-linked ubiquitination IDA
IDA: Inferred from direct assay
26342464 GOA
involved in protein K48-linked ubiquitination IDA
IDA: Inferred from direct assay
36359729 GOA
involved in protein K6-linked ubiquitination IDA
IDA: Inferred from direct assay
36426955 GOA
involved in protein K63-linked ubiquitination IDA
IDA: Inferred from direct assay
36692217 GOA
involved in protein K63-linked ubiquitination IMP
IMP: Inferred from mutant phenotype
26342464 GOA
involved in protein autoubiquitination IDA
IDA: Inferred from direct assay
16880511 GOA
involved in protein destabilization IMP
IMP: Inferred from mutant phenotype
16880511 GOA
involved in protein monoubiquitination IDA
IDA: Inferred from direct assay
16297862 GOA
involved in protein polyubiquitination IDA
IDA: Inferred from direct assay
16297862 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
16472766 GOA
involved in pyroptotic inflammatory response IDA
IDA: Inferred from direct assay
36426955 GOA
involved in response to type II interferon IDA
IDA: Inferred from direct assay
26347139 GOA
involved in stress granule disassembly IDA
IDA: Inferred from direct assay
36692217 GOA
involved in suppression of viral release by host IDA
IDA: Inferred from direct assay
18248090 GOA
Cellular Component GO Annotation Evidence Reference Source
part of SCF ubiquitin ligase complex IDA
IDA: Inferred from direct assay
16880511 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
16316627 GOA
is active in cytoplasmic stress granule IDA
IDA: Inferred from direct assay
36692217 GOA
located in nucleus IDA
IDA: Inferred from direct assay
18845142 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

TRIM21 Protein Structure

zf-C3HC4_4

zf-C3HC4_4: zinc finger of C3HC4-type, RING (16 - 54)

zf-B_box

zf-B_box: B-box zinc finger (88 - 128)

PRY

PRY: SPRY-associated domain (289 - 337)

SPRY

SPRY: SPRY domain (339 - 455)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 475 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase TRIM21

52 kDa Ro protein

TRIM21 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TRIM21 P19474 UBE2I Homo sapiens Q7KZS0
Y2H Prey Pooling
25416956
Intra
TRIM21 P19474 UBE2I Homo sapiens Q7KZS0
Y2H Prey Pooling
32296183
Intra
TRIM21 P19474 UBE2I Homo sapiens Q7KZS0
Validated Y2H
32296183
Intra
TRIM21 P19474 UBE2I Homo sapiens Q7KZS0
Y2H Array
25416956
Intra
TRIM21 P19474 UBE2I Homo sapiens Q7KZS0
Y2H Array
32296183
Intra
TRIM21 P19474 YJU2 Homo sapiens Q9BW85
Validated Y2H
32296183
Intra
TRIM21 P19474 USP15 Homo sapiens Q9Y4E8
Y2H Prey Pooling
25416956
Intra
TRIM21 P19474 TRIM39 Homo sapiens Q9HCM9-2
Validated Y2H
32296183
Intra
TRIM21 P19474 IGFN1 Homo sapiens Q86VF2-5
Validated Y2H
32296183
Intra
TRIM21 P19474 PRKN Homo sapiens O60260-5
Y2H Array
32814053
Intra
TRIM21 P19474 PRKN Homo sapiens O60260-5
Y2H Pooling
32814053
Intra
TRIM21 P19474 PRKN Homo sapiens O60260-5
Validated Y2H
32814053
Intra
TRIM21 P19474 EHHADH Homo sapiens Q08426
Validated Y2H
32296183
Intra
TRIM21 P19474 GMCL1 Homo sapiens Q96IK5
Validated Y2H
32296183
Intra
TRIM21 P19474 GMCL1 Homo sapiens Q96IK5
Y2H Prey Pooling
32296183
Intra
TRIM21 P19474 GMCL1 Homo sapiens Q96IK5
Y2H Array
32296183
Intra
TRIM21 P19474 TCP11L1 Homo sapiens Q9NUJ3
Validated Y2H
32296183
Intra
TRIM21 P19474 DCTN1 Homo sapiens Q14203-5
Validated Y2H
32814053
Intra
TRIM21 P19474 DCTN1 Homo sapiens Q14203-5
Y2H Pooling
32814053
Intra
TRIM21 P19474 DCTN1 Homo sapiens Q14203-5
Y2H Array
32814053
Intra
TRIM21 P19474 XAF1 Homo sapiens Q6GPH4
Y2H Prey Pooling
32296183
Intra
TRIM21 P19474 XAF1 Homo sapiens Q6GPH4
Validated Y2H
32296183
Intra
TRIM21 P19474 XAF1 Homo sapiens Q6GPH4
Y2H Array
32296183
Intra
TRIM21 P19474 GRAP Homo sapiens Q13588
Validated Y2H
25416956
Intra
TRIM21 P19474 GRAP Homo sapiens Q13588
Validated Y2H
32296183
Intra
TRIM21 P19474 TXN2 Homo sapiens Q99757
Validated Y2H
32296183
Intra
TRIM21 P19474 TXN2 Homo sapiens Q99757
Y2H Array
25416956
Intra
TRIM21 P19474 FHOD1 Homo sapiens Q9Y613
Validated Y2H
32296183
Intra
TRIM21 P19474 CFTR Homo sapiens P13569
Anti Bait CoIP
26618866
Intra
TRIM21 P19474 RNF11 Homo sapiens Q9Y3C5
Y2H Pooling
32814053
Intra
TRIM21 P19474 RNF11 Homo sapiens Q9Y3C5
Validated Y2H
32814053
Intra
TRIM21 P19474 RNF11 Homo sapiens Q9Y3C5
Y2H Array
32814053
Intra
TRIM21 P19474 DMAP1 Homo sapiens Q9NPF5
Validated Y2H
32296183
Intra
TRIM21 P19474 DMAP1 Homo sapiens Q9NPF5
Y2H Prey Pooling
32296183
Intra
TRIM21 P19474 DMAP1 Homo sapiens Q9NPF5
Y2H Array
32296183
Intra
TRIM21 P19474 CBX4 Homo sapiens O00257-3
Y2H Prey Pooling
32296183
Intra
TRIM21 P19474 CBX4 Homo sapiens O00257-3
Y2H Array
32296183
Intra
TRIM21 P19474 HTT Homo sapiens P42858
Y2H Pooling
32814053
Intra
TRIM21 P19474 HTT Homo sapiens P42858
Validated Y2H
32814053
Intra
TRIM21 P19474 HTT Homo sapiens P42858
Y2H Array
32814053
Intra
TRIM21 P19474 ZBTB16 Homo sapiens Q05516
Validated Y2H
32296183
Intra
TRIM21 P19474 UCHL1 Homo sapiens P09936
Validated Y2H
32814053
Intra
TRIM21 P19474 UCHL1 Homo sapiens P09936
Y2H Pooling
32814053
Intra
TRIM21 P19474 UCHL1 Homo sapiens P09936
Y2H Array
32814053
Intra
TRIM21 P19474 USP4 Homo sapiens Q13107-1
Y2H
11461834
Intra
TRIM21 P19474 TRIM39 Homo sapiens Q9HCM9
Y2H Array
25416956
Intra
TRIM21 P19474 TRIM39 Homo sapiens Q9HCM9
Y2H Prey Pooling
25416956
Intra
TRIM21 P19474 LNX1 Homo sapiens Q8TBB1
Validated Y2H
32296183
Intra
TRIM21 P19474 EXOC8 Homo sapiens Q8IYI6
Validated Y2H
32296183
Intra
TRIM21 P19474 CWC25 Homo sapiens Q9NXE8
Validated Y2H
32296183
Intra
TRIM21 P19474 TNS4 Homo sapiens Q8IZW8
Validated Y2H
32296183
Intra
TRIM21 P19474 TRIM21 Homo sapiens P19474
Anti Tag CoIP
22493164
Intra
TRIM21 P19474 TRIM21 Homo sapiens P19474
Y2H
22829933
Intra
TRIM21 P19474 TRIM21 Homo sapiens P19474
Y2H Prey Pooling
32296183
Intra
TRIM21 P19474 TRIM21 Homo sapiens P19474
Validated Y2H
32296183
Intra
TRIM21 P19474 TRIM21 Homo sapiens P19474
Y2H Array
25416956
Intra
TRIM21 P19474 TRIM21 Homo sapiens P19474
Y2H Array
32296183
Intra
TRIM21 P19474 VPS9D1 Homo sapiens Q9Y2B5
Validated Y2H
32296183
Intra
TRIM21 P19474 SNCA Homo sapiens P37840
Validated Y2H
32814053
Intra
TRIM21 P19474 SNCA Homo sapiens P37840
Y2H Pooling
32814053
Intra
TRIM21 P19474 SNCA Homo sapiens P37840
Y2H Array
32814053
Cross
TRIM21 P19474 L Lymphocytic choriomeningitis virus P14240
Anti Tag CoIP
29261807
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant TRIM21 Proteins

Cat. No. Product Name Accession Purity
HY-P71791 TRIM21 Protein, Human (P.pastoris, His) P19474 (1M-475Y) ≥95%

Related Diseases

Diseases Alias
Lupus Erythematosus

Lupus

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus, Systemic

Subacute Cutaneous Lupus

Le - [Lupus Erythematosus]

Sjogren Syndrome

Sicca Syndrome

Sjogren'S Syndrome

Sjögren Syndrome

Sjogren-Gougerot Syndrome

Keratoconjunctivitis Sicca

Sjögren'S Syndrome

Xerodermosteosis

Dacryosialoadenopathia Atrophicans

Gougerot-Houwer-Sjogren Syndrome

Gougerot-Sjogren Syndrome

Keratoconjunctivitis Sicca-Xerostomia

Secreto-Inhibitor-Xerodermostenosis

Primary Sjogren Syndrome

Primary Sjogren-Gougerot Syndrome

Sjogrens Syndrome Primary

Sjogrens Syndrome

Dry Eye Syndromes

Heart Block, Congenital

Congenital Heart Block

Heart Block Congenital

Congenital Atrioventricular Block

Subacute Cutaneous Lupus Erythematosus

Lupus Erythematosus Cutaneous Subacute

Lupus Erythematosus, Subacute Cutaneous

Sacle - [Subacute Cutaneous Lupus Erythematosus]

Scle - [Subacute Cutaneous Lupus Erythematosus]

Third-Degree Atrioventricular Block

Third Degree Atrioventricular Block

Complete Atrioventricular Block

Complete Av Block

Third-Degree Block

Complete Atrioventricular Heart Block

Complete Heart Block

Third Degree Atrioventricular Heart Block

Third Degree Heart Block

Complete Heart Block Nos

Chb - [Complete Heart Block]

Idioventricular Rhythm

Av - [Atrioventricular] Block, Complete

Myositis

Idiopathic Inflammatory Myopathy

Idiopathic Inflammatory Myositis

Iim

Imm

Idiopathic Inflammatory Myopathies

Myopathy, Familial Idiopathic Inflammatory

Inflammatory Disorder Of Muscle

Idiopathic Inflammatory Myopathy, Familial

Inflammatory Myopathy, Idiopathic

Myopathies Idiopathic Inflammatory

Familial Idiopathic Inflammatory Myopathy

Systemic Lupus Erythematosus

Lupus Nephritis

SLE

Disseminated Lupus Erythematosus

Systemic Lupus Erythematosus, Susceptibility To

Lupus Erythematosus, Systemic

Lupus Nephritis, Susceptibility To

Libman-Sacks Disease

Systemic Lupus Erythematosus Susceptibility To

Sle - Lupus Erythematosus, Systemic

Le Syndrome

Lupus

Lupus Erythematosus Systemic

Lupus Erythematosus, Systemic, Susceptibility To

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus

Systemic Lupus Erythematosus Nos

Sle - [Systemic Lupus Erythematosus]

Second-Degree Atrioventricular Block

Second-Degree Heart Block

Second Degree Atrioventricular Block

Second Degree Atrioventricular Heart Block

Second Degree Heart Block

Incomplete Atrioventricular Block, Second Degree Nos

Second-Degree Block, Type 1 And 2

Atrioventricular Block, Type 1 And 2

Second Degree Incomplete Atrioventricular Block

Av - [Atrioventricular] Block 2nd

Lymphoid Interstitial Pneumonia

Lymphocytic Interstitial Pneumonia

Lip Disease

Lip Diseases

LIP

Disease Of Lips

Xerophthalmia

Conjunctival Xerosis

Autoimmune Disease Of Exocrine System
Systemic Scleroderma

Scleroderma

Progressive Systemic Sclerosis

Systemic Sclerosis

Scleroderma, Systemic

Scleroderma Syndrome

Dermatosclerosis

Familial Progressive Scleroderma

Progressive Scleroderma

Scleroderma Disease

Scleroderma, Localized

Diffuse Scleroderma

Scleroderma, Familial Progressive

Drug-Induced Lupus Erythematosus

Dile

Dil

Drug-Induced Systemic Lupus Erythematosus

Cutaneous Lupus Erythematosus

Lupus Erythematosus, Cutaneous

Lupus Erythematosus Cutaneous

Lacrimal Apparatus Disease

Lacrimal Apparatus Diseases

Antisynthetase Syndrome

As Syndrome

Anti-Jo1 Syndrome

Keratoconjunctivitis
Phototoxic Dermatitis

Dermatitis, Phototoxic

Photosensitisation Reaction

Photosensitive Dermatitis

Photosensitiveness

Potocki-Shaffer Syndrome

Proximal 11p Deletion Syndrome

Chromosome 11p11.2 Deletion Syndrome

Pss

11p11.2 Deletion

P11pds

Defect11 Syndrome

Deletion Of Chromosome 11p11.2

POSHS

Conjunctival Vascular Disease

Vascular Abnormalities Of Conjunctiva

Conjunctival Vascular Abnormality

Vascular Abnormality Of Conjunctiva

Lymphocytic Choriomeningitis

Lcm

Lymphocytic Meningitis

Lymphocytic Choriomeningitis Virus Encephalomyelitis

Lymphocytic Meningoencephalitis

Non-Arthropod Borne Lymphocytic Choriomeningitis

Lcm - [Lymphocytic Choriomeningitis]

Benign Lymphocytic Meningitis

Meningitis Due To Lymphocytic Choriomeningitis Virus

Parotid Disease

Parotid Diseases

Nonspecific Interstitial Pneumonia

Nsip

Non-Specific Interstitial Pneumonia

Non-Specific Idiopathic Interstitial Pneumonia

Non-Specific Interstitial Pneumonia Nos

Mononeuritis Multiplex
Diffuse Infiltrative Lymphocytosis Syndrome
Sialadenitis

Sialoadenitis

Adenitis, Salivary Gland

Salivary Gland Inflammation

Salivary Gland Adenitis

Sialitis

Inflammation Of Salivary Gland

Inflammation Of Salivary Duct Or Gland

Salivary Glandular Adenitis

Sialoangiitis

Sialoangitis

Sialodochitis

Thrombocytopenia

Low Platelet Count

Low Platelets

Decreased Platelets

Platelet Dysfunction Nos

Dry Eye Syndrome

Dry Eye Syndromes

Dry Eye Disease

Tear Film Insufficiency

Xerophthalmia

Transient Neonatal Thrombocytopenia
Transient Neonatal Neutropenia
Endocardial Fibroelastosis

Endomyocardial Fibroelastosis

Elastomyofibrosis

EFE

Efe - [Endocardial Fibroelastosis]

Primary Endocardial Fibroelastosis

Fibroelastosis Cordis

Fetal Endocarditis

Fibroelastosis

Congenital Endocardial Fibroelastosis

Congenital Valvular Endocarditis

Mononeuritis Of Upper Limb And Mononeuritis Multiplex
Adult Dermatomyositis

Adult Onset Dermatomyositis

Adult Type Dermatomyositis

Keratoconjunctivitis Sicca

Kcs

Dry Eye Syndromes

Keratitis Sicca

Xerophthalmia

Childhood Type Dermatomyositis

Juvenile Dermatomyositis

Juvenile Dm

Childhood Dermatomyositis

Amyopathic Dermatomyositis

Adm

Dermatomyositis Sine Myositis

Dermatomyositis, Childhood Type

Malignant Secondary Hypertension
Atrioventricular Block

Av Block

Libman-Sacks Endocarditis

Libmann-Sachs, Endocarditis In Systemic Lupus Erythematosus

Idiopathic Interstitial Pneumonia

Hamman-Rich Syndrome

Diffuse Idiopathic Pulmonary Fibrosis

Idiopathic Fibrosing Alveolitis

Ipf

Idiopathic Interstitial Pneumonias

Idiopathic Interstitial Pneumonia, Not Otherwise Specified

Pulmonary Fibrosis

Aphthous Stomatitis

Oral Ulcer

Canker Sore

Aphtha

Aphthous Ulceration

Oral Aphthae

Oral Aphthous Ulcer

Canker Sores

Stomatitis, Aphthous

Minor Oral Aphthous Ulceration

Chromosomal Deletion Syndrome
Mononeuropathy

Mononeuropathies

Dacryoadenitis

Dacryocystitis

Mikulicz Disease

Igg4-Related Dacryoadenitis And Sialadenitis

Mikulicz'S Disease

Chronic Dacryoadenitis And Sialadenitis

Mikulicz Syndrome

Mikulicz' Disease

Axonal Neuropathy
Salivary Gland Disease

Salivary Gland Disorders

Salivary Gland Diseases

Non-Neoplastic Salivary Gland Disease

Non-Neoplastic Salivary Gland Disorder

Disorder Of Salivary Gland

Lesion Of Salivary Gland Nos

Exanthem

Exanthema

Rash

Rashes

Parotitis
Autoimmune Disease

Autoimmune Diseases

Autoimmune Hypersensitivity Disease

Hypersensitivity Reaction Type Ii Disease

Type Ii Hypersensitivity Reaction Disease

First-Degree Atrioventricular Block

First Degree Atrioventricular Block

First Degree Heart Block

Incomplete Atrioventricular Block, First Degree

First Degree Atrioventricular Heart Block

Polyclonal Hypergammaglobulinemia

Polyclonal Gammopathy

Diffuse Scleroderma

Diffuse Systemic Sclerosis

Systemic Sclerosis, Diffuse

Scleroderma, Diffuse

Systemic Scleroderma

Progressive System Sclerosis

Dyskinesia Of Esophagus

Esophageal Motility Disorders

Dyskinesia Of Oesophagus

Esophageal Dysmotility

Esophageal Motility Disorder

Oesophageal Dysmotility

Oesophageal Motor Disorder

Esophageal Spasm

Limited Scleroderma

Limited Cutaneous Systemic Sclerosis

Limited Systemic Sclerosis

Systemic Sclerosis Sine Scleroderma

Crest Syndrome

Limited Cutaneous Systemic Scleroderma

Scleroderma, Limited

Systemic Sclerosis, Limited

Progressive Systemic Sclerosis Sine Scleroderma

Scleroderma, Sine

Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome

Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] Syndrome

Raynaud Disease

Raynaud'S Disease

Raynaud Phenomenon

Raynaud'S Syndrome

Raynaud'S

Cold Fingers, Hereditary

Raynaud'S Phenomenon

Raynaud'S Disease/Phenomenon

Raynauds Syndrome

Raynauds Phenomenon

Secondary Raynaud'S Phenomenon

Raynaud Syndrome

Transverse Myelitis

Myelitis Transverse

Myelitis, Transverse

Collagen Disease

Collagen Diseases

Collagen Disorder

Temporal Arteritis

Polymyalgia Rheumatica

Giant Cell Arteritis

Cranial Arteritis

Horton Disease

Gca

Horton'S Disease

Rhizomelic Pseudopolyarthritis

Arteritis Cranialis

Arteritis Temporalis

Horton'S Arteritis

Horton'S Giant Cell Arteritis

Horton'S Temporal Arteritis

Horton'S Syndrome

Gca - [Giant Cell Arteritis]

Senile Arthritis

Polymyalgia Arteritica

Pmr - [Polymyalgia Rheumatica]

Forestier-Certonciny Syndrome

Rheumatic Polymyalgia

Polymyalgia

Telangiectasis

Telangiectasia

Autoimmune Disease Of Musculoskeletal System
Punctate Epithelial Keratoconjunctivitis

Punctate Keratitis

Thygeson Superficial Punctate Keratitis

Thygeson'S Superficial Punctate Keratitis

Thygeson Superficial Punctate Keratopathy

Punctate Epithelial Keratitis

Pericardium Disease
Hypersensitivity Reaction Type Iv Disease

Immunoproliferative Disorders

Immunoproliferative Disease

Autoimmune Disease Of Cardiovascular System
Chromosomal Disease

Chromosomal Disorders

Congenital Chromosomal Disease

Heart Conduction Disease

Conduction Disorder Of The Heart

Heart Rhythm Disease

Muscle Tissue Disease
Hyperlipoproteinemia, Type V

Hyperlipoproteinemia Type V

Hyperchylomicronemia, Late-Onset

Familial Type 5 Hyperlipoproteinemia

Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial

Hyperlipidemia, Type V

Hyperlipemia, Mixed

Hyperlipemia, Combined Fat And Carbohydrate-Induced

Familial Hyperlipoproteinemia Type V

Fredrickson Type V Lipaemia

Hyperlipoproteinemia Type 5

Hyperchylomicronemia Late Onset

Hyperlipemia Combined Fat And Carbohydrate-Induced

Hyperlipemia Mixed

Hyperlipidemia Type V

Mixed Hyperlipemia

Type V Hyperlipoproteinemia

Hyperlipoproteinemia 5

HLPP5

Hyperlipidemia, Familial Combined

Mixed Hyperlipidemia

Primary Biliary Cholangitis

Primary Biliary Cirrhosis

Biliary Liver Cirrhosis

Chronic Nonsuppurative Destructive Cholangitis

Familial Primary Biliary Cirrhosis

Pbc

Hanot Syndrome

Cholestatic Cirrhosis

Biliary Cirrhosis Primary

Liver Cirrhosis, Biliary

Hanot'S Cirrhosis

Biliary Cirrhosis

Pericholangiolic Biliary Cirrhosis

Tannhauser-Magendantz Syndrome

Hanot-Rossle Syndrome

Hypertrophic Cirrhosis

Todd Cirrhosis

Hanot Cirrhosis

Charcot Cirrhosis

Mahon-Tannhauser Syndrome

Toxic Cirrhosis

Hypertrophic Biliary Cirrhosis

Monolobular Cirrhosis

Unilobar Cirrhosis

Xanthomatous Biliary Cirrhosis

Skin Disease

Skin Diseases

Genodermatosis

Abnormality Of The Skin

Skin Diseases, Genetic

Skin And Subcutaneous Tissue Disease

Dermatologic Disorders

Myopathy

Muscular Diseases

Myopathies

Connective Tissue Disease

Connective Tissue Diseases

Connective Tissue Disorder

Abnormality Of Connective Tissue

Disorder Of Connective Tissue

Connective Tissue Disorders

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus TRIM21 RGD RGD:1305795
Bos taurus TRIM21 VGNC VGNC:36319
Felis catus TRIM21 VGNC VGNC:66530
Mus musculus TRIM21 MGD MGI:106657
Macaca mulatta TRIM21 VGNC VGNC:78556
Canis familiaris TRIM21 VGNC VGNC:47808
Others TRIM21 NCBI