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: FGL1 ENSPTRG00000020025

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Description

fibrinogen like 1 [Source:VGNC Symbol;Acc:VGNC:871]

Location

Chromosome 8: 17,078,449-17,110,021 reverse strand.

Pan_tro_3.0:CM000322.4

About this gene

This gene has 1 transcript (splice variant), 125 orthologues and 31 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000037101.5	FGL1-201	2134	312aa	ENSPTRP00000034286.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8KIH6 A0A6D2WXN8	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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