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

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Gene: si:ch211-156j16.1 ENSDARG00000092035

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Description

si:ch211-156j16.1 [Source:ZFIN;Acc:ZDB-GENE-030131-4106]

Gene Synonyms

fc72g03, im:7049455, wu:fc72g03

Location

Chromosome 8: 26,818,446-26,838,845 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000134987.3	si:ch211-156j16.1-201	1786	171aa	ENSDARP00000121374.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0V2Z2	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,
ENSDART00000138835.2	si:ch211-156j16.1-202	675	186aa	ENSDARP00000117986.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0V2Z1	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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