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

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Gene: fmn2b ENSDARG00000061778

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Description

formin 2b [Source:ZFIN;Acc:ZDB-GENE-080225-35]

Gene Synonyms

im:7158925

Location

Chromosome 12: 47,446,158-47,541,290 forward strand.

GRCz11:CM002896.2

About this gene

This gene has 3 transcripts (splice variants), 99 orthologues, 25 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000185689.1	fmn2b-203	4440	1479aa	ENSDARP00000148541.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QAK8	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSDART00000152857.3	fmn2b-202	5336	1454aa	ENSDARP00000127455.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AB32TYQ3	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,
ENSDART00000105328.5	fmn2b-201	4494	1454aa	ENSDARP00000096100.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AB32TYQ3	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,

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Summary

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