Nop10 Gene Summary [Mouse]

Predicted to enable box H/ACA snoRNA binding activity and telomerase RNA binding activity. Predicted to be involved in snRNA pseudouridine synthesis; snoRNA guided rRNA pseudouridine synthesis; and telomere maintenance via telomerase. Predicted to be located in nuclear body. Predicted to be part of box H/ACA snoRNP complex and box H/ACA telomerase RNP complex. Is expressed in several structures, including alimentary system; brain; genitourinary system; hemolymphoid system; and integumental system. Human ortholog(s) of this gene implicated in autosomal recessive dyskeratosis congenita 1. Orthologous to human NOP10 (NOP10 ribonucleoprotein). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Nop10
Official Name
NOP10 ribonucleoprotein [Source:MGI Symbol;Acc:MGI:1913431]
Ensembl ID
ENSMUSG00000027133
Bio databases IDs NCBI: 66181 Ensembl: ENSMUSG00000027133
Aliases NOP10 ribonucleoprotein
Synonyms 1110036B12Rik, CHINE2, DKCB1, LOC687899, NOLA3, NOP10P, NOP10 ribonucleoprotein, PFBMFT9
Species
Mouse, Mus musculus
OrthologiesHumanRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Nop10 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • snoRNA binding
  • protein binding
  • Nucleolar RNA-binding protein, Nop10p family
  • RNA binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • telomere-related pulmonary fibrosis and/or bone marrow failure syndrome type 9
  • autosomal recessive dyskeratosis congenita type 1
  • cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2
regulated by
  • CD 437
  • LCK
  • EIF4E
  • CST5
  • ST1926
  • OVA-8
  • Lethal toxin
role in cell
  • telomere-length maintenance

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Nucleus
  • interchromatin granule cluster fractions
  • dense fibrillar component
  • nucleoplasm
  • nucleoli
  • nuclear bodies
  • Cajal bodies
  • perikaryon

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Nop10 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • pseudouridine synthesis
  • rRNA pseudouridine synthesis
  • snRNA pseudouridine synthesis
  • telomere maintenance via telomerase

Cellular Component

Where in the cell the gene product is active
  • box H/ACA snoRNP complex
  • nuclear body
  • box H/ACA scaRNP complex
  • telomerase holoenzyme complex
  • small nucleolar ribonucleoprotein complex
  • nucleoplasm

Molecular Function

What the gene product does at the molecular level
  • RNA binding
  • protein binding
  • telomeric RNA binding
  • box H/ACA snoRNA binding

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.