Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: GRSF1 ENSBTAG00000008577

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Description

G-rich RNA sequence binding factor 1 [Source:VGNC Symbol;Acc:VGNC:29667]

Location

Primary_assembly 6: 86,196,005-86,250,072 reverse strand.

ARS-UCD1.3:CM008173.2

About this gene

This gene has 3 transcripts (splice variants), 157 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000011313.7	GRSF1-203	3199	610aa	ENSBTAP00000011313.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0JNI7	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,
ENSBTAT00000125886.1	GRSF1-202	3411	608aa	ENSBTAP00000103358.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000039551.5	GRSF1-201	2574	362aa	ENSBTAP00000039341.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6QPB2	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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