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: Magoh ENSRNOG00000012778

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Description

mago homolog, exon junction complex subunit [Source:RGD Symbol;Acc:1305174]

Gene Synonyms

LOC298385

Location

Primary_assembly 5: 127,868,055-127,875,384 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 88 orthologues and 1 paralogue.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000017422.8	Magoh-201	691	161aa	ENSRNOP00000017421.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q8H0	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,

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Paralogues

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