Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: FMN2 ENSOCUG00000003998

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Description

formin 2 [Source:HGNC Symbol;Acc:HGNC:14074]

Location

Chromosome 16: 30,223,636-30,577,805 forward strand.

OryCun2.0:CM000805.1

About this gene

This gene has 2 transcripts (splice variants), 134 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000030541.3	FMN2-201	5487	1828aa	ENSOCUP00000023697.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1U2U4	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,
ENSOCUT00000004002.4	FMN2-202	5475	1824aa	ENSOCUP00000003468.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SKV9	-

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Summary

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