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
External references
Supporting evidence
ID History
- Gene history

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Gene: Myadml2 ENSRNOG00000036681

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Description

myeloid-associated differentiation marker-like 2 [Source:RGD Symbol;Acc:1311499]

Gene Synonyms

LOC303744, MGC189381, RGD1311499

Location

Primary_assembly 10: 106,421,419-106,426,224 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 181 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000124840.1	Myadml2-202	3962	307aa	ENSRNOP00000101097.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000054948.5	Myadml2-201	2207	307aa	ENSRNOP00000051831.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2RZ87	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,

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Summary

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