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

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Gene: Dmxl1 ENSRNOG00000024671

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Description

Dmx-like 1 [Source:RGD Symbol;Acc:1307692]

Gene Synonyms

LOC307429

Location

Primary_assembly 18: 45,179,551-45,356,406 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 5 transcripts (splice variants), 208 orthologues, 1 paralogue and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000113305.2	Dmxl1-203	11141	3064aa	ENSRNOP00000082026.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZU67	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 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,
ENSRNOT00000031812.7	Dmxl1-201	11090	3047aa	ENSRNOP00000033699.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AA13	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,
ENSRNOT00000094956.2	Dmxl1-202	10997	3016aa	ENSRNOP00000088454.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9G2	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,
ENSRNOT00000130737.1	Dmxl1-204	10614	3061aa	ENSRNOP00000101656.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000153521.1	Dmxl1-205	10473	2788aa	ENSRNOP00000112073.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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