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: grsf1 ENSDARG00000053021

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Description

G-rich RNA sequence binding factor 1 [Source:ZFIN;Acc:ZDB-GENE-060825-196]

Gene Synonyms

wu:fb62c04, zgc:153305

Location

Chromosome 5: 42,943,972-42,950,963 reverse strand.

GRCz11:CM002889.2

About this gene

This gene has 2 transcripts (splice variants), 77 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000149868.3	grsf1-202	1451	403aa	ENSDARP00000124123.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F8W4V6	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,
ENSDART00000149549.2	grsf1-201	885	145aa	ENSDARP00000125086.1	Nonsense mediated decay	F8W5I2	-

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Summary

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