Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: DMRT2 ENSSSCG00000005233

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Description

doublesex and mab-3 related transcription factor 2 [Source:VGNC Symbol;Acc:VGNC:87351]

Location

Primary_assembly 1: 220,745,502-220,757,324 reverse strand.

Sscrofa11.1:CM000812.5

About this gene

This gene has 3 transcripts (splice variants), 208 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000080473.2	DMRT2-203	7170	561aa	ENSSSCP00000066791.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A480RGK4 A0A4X1W5X0	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,
ENSSSCT00000086788.2	DMRT2-202	6240	404aa	ENSSSCP00000059902.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1W848 A0A5G2Q9C6	-
ENSSSCT00000096153.1	DMRT2-201	2505	227aa	ENSSSCP00000080806.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1W737 A0A8W4FMU2	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Orthologues

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