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

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Gene: FOSL1 ENSSSCG00000012967

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Description

FOS like 1, AP-1 transcription factor subunit [Source:VGNC Symbol;Acc:VGNC:88191]

Location

Primary_assembly 2: 6,430,153-6,436,173 forward strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000044856.2	FOSL1-202	1719	271aa	ENSSSCP00000056518.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BK33 A0A8D0TLH5	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,
ENSSSCT00000014174.4	FOSL1-201	962	235aa	ENSSSCP00000013788.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1B3R4 F1RU26	-

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Summary

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