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

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Gene: MAGIX ENSSSCG00000012295

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Description

MAGI family member, X-linked [Source:HGNC Symbol;Acc:HGNC:30006]

Location

Primary_assembly X: 43,207,062-43,211,635 forward strand.

Sscrofa11.1:CM000830.5

About this gene

This gene has 2 transcripts (splice variants), 265 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000013444.6	MAGIX-201	1258	331aa	ENSSSCP00000013084.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1PK90 F1RW42	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,
ENSSSCT00000087538.2	MAGIX-202	1021	252aa	ENSSSCP00000066453.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QNI2 A0A8D1TUH0	-

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Summary

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