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

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Gene: FIGLA ENSPTRG00000012033

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Description

folliculosis specific bHLH transcription factor [Source:VGNC Symbol;Acc:VGNC:255]

Location

Chromosome 2A: 72,244,984-72,258,244 reverse strand.

Pan_tro_3.0:CM000315.3

About this gene

This gene has 2 transcripts (splice variants), 189 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000022390.6	FIGLA-201	660	219aa	ENSPTRP00000020660.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2YAY0 H2QI28	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,
ENSPTRT00000098654.1	FIGLA-202	744	217aa	ENSPTRP00000066304.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RNN0	-

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Summary

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