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

Configure this page

Share this page

Bookmark this page

.

Gene: fmnl2a ENSDARG00000012586

.

Description

formin-like 2a [Source:ZFIN;Acc:ZDB-GENE-081105-70]

Gene Synonyms

fmnl2, si:ch211-279a7.1

Location

Chromosome 9: 4,730,398-4,856,767 reverse strand.

GRCz11:CM002893.2

About this gene

This gene has 3 transcripts (splice variants), 218 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000138015.3	fmnl2a-203	3659	1077aa	ENSDARP00000118722.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QKR1	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSDART00000133090.4	fmnl2a-202	4842	521aa	ENSDARP00000115853.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q6D2	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000016814.10	fmnl2a-201	3267	1088aa	ENSDARP00000024319.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QDA5	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,

.

Summary

.

.