Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: zgc:171775 ENSDARG00000058381

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Description

zgc:171775 [Source:ZFIN;Acc:ZDB-GENE-030131-4309]

Gene Synonyms

fc89f08, wu:fc89f08

Location

Chromosome 23: 10,146,542-10,165,033 forward strand.

GRCz11:CM002907.2

About this gene

This gene has 3 transcripts (splice variants), 96 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000048073.7	zgc:171775-201	3962	359aa	ENSDARP00000048072.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QHF2	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,
ENSDART00000145026.3	zgc:171775-202	534	100aa	ENSDARP00000116511.1	Nonsense mediated decay	E9QBD3	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000145232.2	zgc:171775-203	452	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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