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

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Gene: Nxn ENSRNOG00000008178

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Description

nucleoredoxin [Source:RGD Symbol;Acc:1310489]

Gene Synonyms

LOC360577

Location

Primary_assembly 10: 61,607,568-61,745,807 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 142 orthologues, 2 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000114535.2	Nxn-202	2699	435aa	ENSRNOP00000085662.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A4C2	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,
ENSRNOT00000050232.5	Nxn-201	2336	407aa	ENSRNOP00000047264.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A0M2	-

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Summary

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