2. Gene
  3. URB1 - URB1 ribosome biogenesis homolog Gene

URB1 - URB1 ribosome biogenesis homolog Gene

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

Also known as NPA1; C21orf108

Gene ID: 9875 | Gene type: protein coding

About URB1

Cytogenetic location: 21q22.11 Genomic coordinates (GRCh38): 21:32,311,018-32,393,012 (from NCBI)

This gene has 3 transcripts (splice variants) and 196 orthologues. Ubiquitous expression in testis (RPKM 5.5), endometrium (RPKM 5.1) and 25 other tissues.

Summary

Enables RNA binding activity. Predicted to be involved in maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) and maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Located in fibrillar center. [provided by Alliance of Genome Resources, Apr 2022]

URB1 Products(1)

mRNA Protein Name
NM_014825.3 NP_055640.2 nucleolar pre-ribosomal-associated protein 1

URB1 Protein Structure

Npa1

Npa1: Ribosome 60S biogenesis N-terminal (74 - 394)

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  • 2271 a.a.
Protein Preferred Names Protein Names

nucleolar pre-ribosomal-associated protein 1

URB1 ribosome biogenesis 1 homolog

Related Diseases

Diseases Alias
Tick Paralysis
X-Linked Intellectual Disability-Short Stature-Overweight Syndrome

Mrx12

Mrx35

X-Linked Mental Retardation 12

X-Linked Mental Retardation 35
Niemann-Pick Disease, Type B

Niemann-Pick Disease Type B

Acid Sphingomyelinase Deficiency, Visceral Type

Asmd, Visceral Type

Niemann Pick Disease Type B

Chronic Visceral Acid Sphingomyelinase Deficiency

Chronic Visceral Asmd

Npd-B

Niemann-Pick Disease B

NPDB

Niemann-Pick Disease Adult Non-Neuronopathic Form

Niemann-Pick Disease Intermediate With Visceral Involvement And Rapid Progression

Niemann-Pick Disease Type E

Niemann-Pick Disease Type F

Niemann-Pick Disease Type I

Niemann-Pick Disease Visceral Form

Npb

Sphingomyelinase Deficiency

Sphingomyelin Lipidosis

Niemann-Picks Disease Type B

Niemann-Pick Disease, Type E

Niemann-Pick Diseases

Niemann-Pick Disease, Type A
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-RS15505 URB1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus URB1 RGD RGD:1304621
Canis familiaris URB1 VGNC VGNC:53050
Macaca mulatta URB1 VGNC VGNC:79074
Felis catus URB1 VGNC VGNC:66851
Bos taurus URB1 VGNC VGNC:53611
Mus musculus URB1 MGD MGI:2146468