Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
Phenotypes
Genetic Variation
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Gene expression
Pathway
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External references
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ID History
- Gene history

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Gene: Vgf ENSRNOG00000001416

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Description

VGF nerve growth factor inducible [Source:RGD Symbol;Acc:69399]

Gene Synonyms

LOC100909521

Location

Primary_assembly 12: 19,637,320-19,640,341 reverse strand.

mRatBN7.2:CM026985.1

About this gene

This gene has 1 transcript (splice variant), 72 orthologues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000041808.3	Vgf-201	2636	617aa	ENSRNOP00000050024.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LP80 P20156	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,

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Summary

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