NOL10 - nucleolar protein 10 Gene

Also Known as PQBP5

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79954

About NOL10

Cytogenetic location: 2p25.1 Genomic coordinates (GRCh38): 2:10,570,754-10,689,975 (from NCBI)

This gene has 22 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in testis (RPKM 4.5), adrenal (RPKM 4.0) and 25 other tissues.

Summary

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

NOL10 Products (3)

mRNA Protein Name
NM_001261392.2 NP_001248321.1 nucleolar protein 10 isoform 2
NM_001261394.2 NP_001248323.1 nucleolar protein 10 isoform 3
NM_024894.4 NP_079170.2 nucleolar protein 10 isoform 1

NOL10 Protein Structure

NUC153

NUC153: NUC153 domain (482 - 508)

  • 0
  • 200
  • 400
  • 600
  • 688 a.a.
Protein Preferred Names Protein Names

nucleolar protein 10

  • H_NH0074G24.1

Related Diseases

Diseases Alias
Renpenning Syndrome 1

  • Renpenning Syndrome

  • Golabi-Ito-Hall Syndrome

  • Mrxs3

  • Mrxs8

  • X-Linked Intellectual Disability Due To Pqbp1 Mutations

  • RENS1

  • Sutherland-Haan X-Linked Mental Retardation Syndrome

  • Shs

  • Mrx55

  • X-Linked Intellectual Disability, Renpenning Type

  • Sutherland-Haan Syndrome

  • Mental Retardation, X-Linked, Renpenning Type

  • Mental Retardation, X-Linked, With Spastic Diplegia

  • Mental Retardation, X-Linked, Syndromic 3

  • Mental Retardation, X-Linked, Syndromic 8

  • Mental Retardation, X-Linked 55

  • Syndromic X-Linked Mental Retardation 8

  • X-Linked Mental Retardation Renpenning Type

  • X-Linked Mental Retardation With Spastic Diplegia

  • Sutherland-Haan X-Linked Intellectual Disability Syndrome

  • X-Linked Intellectual Disability With Spastic Diplegia

  • Hamel Cerebropalatocardiac Syndrome

  • Porteous Syndrome

  • X-Linked Intellectual Deficit Due To Pqbp1 Mutations

  • X-Linked Intellectual Deficit, Renpenning Type

  • X-Linked Intellectual Disability, Sutherland-Haan Type

  • Hamel Cerebro-Palato-Cardiac Syndrome

  • Renpenning Syndrome, Type 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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Nom du produit
Effect
Pureté
Rare Diseases
HY-RS09411 NOL10 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus NOL10 RGD RGD:1359447
Macaca mulatta NOL10 VGNC VGNC:75260
Canis familiaris NOL10 VGNC VGNC:43880
Mus musculus NOL10 MGD MGI:2684913
Bos taurus NOL10 VGNC VGNC:32154
Felis catus NOL10 VGNC VGNC:63850
Others NOL10 NCBI