Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
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Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Gene: Nsa2 ENSRNOG00000016530

Description

NSA2 ribosome biosis factor [Source:RGD Symbol;Acc:621335]

Gene Synonyms

Cdk105, MGC112601, Tinp1

Location

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant), 269 orthologues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022138.8	Nsa2-201	1130	260aa	ENSRNOP00000022138.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I520 F7EX15	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,

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