Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
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  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Nol10 ENSRNOG00000005344

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Description

nucleolar protein 10 [Source:RGD Symbol;Acc:1359447]

Gene Synonyms

LOC313981

Location

Primary_assembly 6: 45,872,960-45,954,066 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants), 199 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000007169.8	Nol10-201	2841	688aa	ENSRNOP00000007169.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q66H99	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSRNOT00000138921.1	Nol10-203	2694	639aa	ENSRNOP00000103722.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000118181.2	Nol10-202	2128	677aa	ENSRNOP00000076483.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZK33	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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