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: Magec2l1 ENSRNOG00000031222

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Description

MAGE family member C2 like 1 [Source:RGD Symbol;Acc:1561327]

Gene Synonyms

LOC317593, RGD1561327

Location

Primary_assembly X: 144,565,383-144,746,910 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 103 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118327.2	Magec2l1-202	2369	419aa	ENSRNOP00000093522.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LUV1	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 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,
ENSRNOT00000048467.5	Magec2l1-201	2230	419aa	ENSRNOP00000039887.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LUV1	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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