Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: F2 ENSRNOG00000016325

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Description

coagulation factor II, thrombin [Source:RGD Symbol;Acc:61996]

Location

Primary_assembly 3: 98,051,960-98,065,246 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 85 orthologues, 1 paralogue and is associated with 109 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022233.7	F2-201	1981	617aa	ENSRNOP00000022233.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HND0 G3V843	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,
ENSRNOT00000095299.2	F2-202	1848	610aa	ENSRNOP00000086700.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABS3	-

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Summary

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