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

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Gene: NTNG2 ENSDARG00000077367

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Description

netrin G2 [Source:HGNC Symbol;Acc:HGNC:14288]

Location

Chromosome 8: 11,993,150-12,111,461 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 4 transcripts (splice variants), 155 orthologues and 40 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000114432.4	NTNG2-203	1569	522aa	ENSDARP00000099713.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,
ENSDART00000191519.1	NTNG2-204	1128	375aa	ENSDARP00000147362.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSDART00000132492.2	NTNG2-201	1031	343aa	ENSDARP00000123242.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000138101.2	NTNG2-202	705	156aa	ENSDARP00000118610.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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