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: MSGN1 ENSSSCG00000026538

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Description

mesogenin 1 [Source:VGNC Symbol;Acc:VGNC:90417]

Location

Primary_assembly 3: 120,034,043-120,034,624 reverse strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 1 transcript (splice variant), 176 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000028291.3	MSGN1-201	582	194aa	ENSSSCP00000026792.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U623 F1SCS7	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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Summary

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