Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FMNL3 ENSSSCG00000025114

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Description

formin like 3 [Source:VGNC Symbol;Acc:VGNC:88169]

Location

Primary_assembly 5: 15,592,666-15,646,046 reverse strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 3 transcripts (splice variants), 209 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000025087.4	FMNL3-202	4231	1027aa	ENSSSCP00000026968.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0XCZ0 I3LS77	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,
ENSSSCT00000025920.4	FMNL3-203	4158	1027aa	ENSSSCP00000026483.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1WCJ6 I3LQV1	-
ENSSSCT00000024676.4	FMNL3-201	4080	976aa	ENSSSCP00000026546.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LR14	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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