RO60 - Ro60, Y RNA binding protein Gene

Also Known as SSA2; RORNP; TROVE2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6738

About RO60

Cytogenetic location: 1q31.2 Genomic coordinates (GRCh38): 1:193,059,612-193,091,777 (from NCBI)

This gene has 12 transcripts (splice variants) and 198 orthologues. Ubiquitous expression in brain (RPKM 6.6), prostate (RPKM 5.8) and 25 other tissues.

Summary

Enables RNA binding activity. Involved in cellular response to interferon-alpha and regulation of gene expression. Located in cytosol and nucleoplasm. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Apr 2022]

RO60 Products (6)

mRNA Protein Name
NM_001042369.2 NP_001035828.1 RNA-binding protein RO60 isoform 1
NM_001042370.2 NP_001035829.2 RNA-binding protein RO60 isoform 3
NM_001173524.2 NP_001166995.1 RNA-binding protein RO60 isoform 2
NM_001173525.1 NP_001166996.1 RNA-binding protein RO60 isoform 4
NM_001331020.2 NP_001317949.1 RNA-binding protein RO60 isoform 5
NM_004600.5 NP_004591.2 RNA-binding protein RO60 isoform 2
Molecular Function GO Annotation Evidence References Source
enables RNA binding IDA
IDA: Inferred from direct assay
26382853 GOA
Biological Process GO Annotation Evidence References Source
involved in cellular response to interferon-alpha IDA
IDA: Inferred from direct assay
26382853 GOA
involved in regulation of gene expression IDA
IDA: Inferred from direct assay
26382853 GOA
Cellular Component GO Annotation Evidence References Source
part of ribonucleoprotein complex IDA
IDA: Inferred from direct assay
17289661 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

RO60 Protein Structure

TROVE

TROVE: TROVE domain (17 - 369)

DUF2201

DUF2201: VWA-like domain (DUF2201) (373 - 479)

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  • 538 a.a.
Protein Preferred Names Protein Names

RNA-binding protein RO60

  • 60 kDa ribonucleoprotein Ro

Related Diseases

Diseases Alias
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

Lupus Erythematosus
  • Lupus

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus, Systemic

  • Subacute Cutaneous Lupus

  • Le - [Lupus Erythematosus]

Heart Block, Congenital
  • Congenital Heart Block

  • Heart Block Congenital

  • Congenital Atrioventricular Block

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]

Xerophthalmia
  • Conjunctival Xerosis

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

Autoimmune Disease Of Exocrine System
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

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

Endocardial Fibroelastosis
  • Endomyocardial Fibroelastosis

  • Elastomyofibrosis

  • EFE

  • Efe - [Endocardial Fibroelastosis]

  • Primary Endocardial Fibroelastosis

  • Fibroelastosis Cordis

  • Fetal Endocarditis

  • Fibroelastosis

  • Congenital Endocardial Fibroelastosis

  • Congenital Valvular Endocarditis

Libman-Sacks Endocarditis
  • Libmann-Sachs, Endocarditis In Systemic Lupus Erythematosus

Keratoconjunctivitis Sicca
  • Kcs

  • Dry Eye Syndromes

  • Keratitis Sicca

  • Xerophthalmia

Antisynthetase Syndrome
  • As Syndrome

  • Anti-Jo1 Syndrome

Cutaneous Lupus Erythematosus
  • Lupus Erythematosus, Cutaneous

  • Lupus Erythematosus Cutaneous

Atrioventricular Block
  • Av Block

Neonatal Myasthenia Gravis
  • Myasthenia Gravis, Neonatal

Lacrimal Apparatus Disease
  • Lacrimal Apparatus Diseases

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

Dry Eye Syndrome
  • Dry Eye Syndromes

  • Dry Eye Disease

  • Tear Film Insufficiency

  • Xerophthalmia

Autoimmune Disease
  • Autoimmune Diseases

  • Autoimmune Hypersensitivity Disease

  • Hypersensitivity Reaction Type Ii Disease

  • Type Ii Hypersensitivity Reaction Disease

Childhood Type Dermatomyositis
  • Juvenile Dermatomyositis

  • Juvenile Dm

  • Childhood Dermatomyositis

  • Amyopathic Dermatomyositis

  • Adm

  • Dermatomyositis Sine Myositis

  • Dermatomyositis, Childhood Type

Chromosomal Deletion Syndrome
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

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
Bos taurus RO60 VGNC VGNC:36379
Rattus norvegicus RO60 RGD RGD:1305083
Macaca mulatta RO60 VGNC VGNC:100063
Mus musculus RO60 MGD MGI:106652
Felis catus RO60 VGNC VGNC:64713
Canis familiaris RO60 VGNC VGNC:47864
Others RO60 NCBI