Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Grsf1 ENSRNOG00000003392

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Description

G-rich RNA sequence binding factor 1 [Source:RGD Symbol;Acc:1310858]

Gene Synonyms

LOC305256

Location

Primary_assembly 14: 19,696,393-19,713,431 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 3 transcripts (splice variants), 157 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000104596.2	Grsf1-203	3313	625aa	ENSRNOP00000080427.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G4I5	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,
ENSRNOT00000086571.3	Grsf1-202	2415	381aa	ENSRNOP00000068892.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JTY6	-
ENSRNOT00000004551.9	Grsf1-201	2402	362aa	ENSRNOP00000004551.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LRK4	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,

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Summary

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