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

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Gene: fosl1a ENSDARG00000015355

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Description

FOS like 1, AP-1 transcription factor subunit a [Source:ZFIN;Acc:ZDB-GENE-061207-7]

Gene Synonyms

fosl1, sb:eu506, si:ch211-145o7.4

Location

Chromosome 14: 30,739,476-30,747,686 reverse strand.

GRCz11:CM002898.2

About this gene

This gene has 2 transcripts (splice variants), 188 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000008373.9	fosl1a-201	3817	346aa	ENSDARP00000011823.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A2CEM8	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,
ENSDART00000146767.2	fosl1a-202	870	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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