Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: VGF ENSBTAG00000009868

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Description

VGF nerve growth factor inducible [Source:VGNC Symbol;Acc:VGNC:36790]

Location

Primary_assembly 25: 35,569,087-35,591,773 forward strand.

ARS-UCD2.0:CM008192.2

About this gene

This gene has 2 transcripts (splice variants) and 72 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000091517.1	VGF-201	11348	618aa	ENSBTAP00000076730.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F2Z4E0	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,
ENSBTAT00000013014.5	VGF-202	5914	618aa	ENSBTAP00000013014.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F2Z4E0	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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