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

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Gene: MAGIX ENSBTAG00000013278

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Description

MAGI family member, X-linked [Source:VGNC Symbol;Acc:VGNC:56927]

Location

Primary_assembly X: 87,208,764-87,214,030 forward strand.

ARS-UCD2.0:CM008197.2

About this gene

This gene has 4 transcripts (splice variants), 259 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000017659.6	MAGIX-201	1678	435aa	ENSBTAP00000017659.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MSW3	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,
ENSBTAT00000114411.2	MAGIX-203	2135	363aa	ENSBTAP00000082961.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SK42	-
ENSBTAT00000134864.2	MAGIX-202	1504	253aa	ENSBTAP00000087779.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SUY6	-
ENSBTAT00000127828.2	MAGIX-204	1076	277aa	ENSBTAP00000076798.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RWJ2	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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