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

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Gene: NLGN2 ENSBTAG00000020252

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Description

neuroligin 2 [Source:VGNC Symbol;Acc:VGNC:55861]

Location

Primary_assembly 19: 27,087,115-27,098,969 forward strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 2 transcripts (splice variants), 231 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000026987.7	NLGN2-201	4777	843aa	ENSBTAP00000026987.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N104	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,
ENSBTAT00000111362.1	NLGN2-202	4702	818aa	ENSBTAP00000092413.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T3R0	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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