Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Glrx3 ENSRNOG00000016227

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Description

glutaredoxin 3 [Source:RGD Symbol;Acc:69414]

Gene Synonyms

MGC105380, Txnl2

Location

Primary_assembly 1: 201,671,481-201,701,717 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 227 orthologues, 1 paralogue and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022406.8	Glrx3-201	1235	337aa	ENSRNOP00000022406.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9JLZ1-1	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000083316.3	Glrx3-202	1406	287aa	ENSRNOP00000073509.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K5P8	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000107315.2	Glrx3-203	1148	269aa	ENSRNOP00000079546.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZN19	-
ENSRNOT00000109827.2	Glrx3-204	972	323aa	ENSRNOP00000091412.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AG27	-

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Summary

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