Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: si:ch211-214c7.4 ENSDARG00000069595

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Description

si:ch211-214c7.4 [Source:ZFIN;Acc:ZDB-GENE-030131-6275]

Gene Synonyms

fi41g12, wu:fi41g12

Location

Chromosome 1: 45,707,219-45,744,854 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants) and 85 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000143363.4	si:ch211-214c7.4-201	7673	1505aa	ENSDARP00000117940.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6P0E6	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,
ENSDART00000149116.2	si:ch211-214c7.4-202	3872	372aa	ENSDARP00000124382.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F8W3K0	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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