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

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Dmxl2 ENSRNOG00000009170

.

Description

Dmx-like 2 [Source:RGD Symbol;Acc:1586163]

Gene Synonyms

Dmxl2-ps1, LOC315676

Location

Primary_assembly 8: 63,637,314-63,781,116 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 3 transcripts (splice variants), 206 orthologues, 1 paralogue and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000066197.6	Dmxl2-201	10668	3056aa	ENSRNOP00000059323.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M3W5	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000114414.2	Dmxl2-202	10605	3035aa	ENSRNOP00000079423.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMW1	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,
ENSRNOT00000162541.1	Dmxl2-203	10240	2884aa	ENSRNOP00000103062.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Strains

.

Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

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

.

Personal Data