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

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Gene: Fgl1 ENSRNOG00000010714

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Description

fibrinogen-like 1 [Source:RGD Symbol;Acc:620169]

Gene Synonyms

Frep1, Lfire1, MGC108569

Location

Primary_assembly 16: 57,824,200-57,854,429 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants), 125 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000090644.3	Fgl1-202	1235	331aa	ENSRNOP00000073912.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R9U7	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,
ENSRNOT00000014248.8	Fgl1-201	1217	278aa	ENSRNOP00000014248.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5M8C6 Q8K583	-

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Summary

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