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

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Gene: nlgn3a ENSDARG00000104786

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Description

neuroligin 3a [Source:NCBI gene (formerly Entrezgene);Acc:562702]

Location

Chromosome 14: 14,224,730-14,534,457 forward strand.

GRCz11:CM002898.2

About this gene

This gene has 6 transcripts (splice variants), 240 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000174760.2	nlgn3a-203	3367	878aa	ENSDARP00000143446.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IJ74	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,
ENSDART00000168749.2	nlgn3a-202	4525	838aa	ENSDARP00000138375.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IQV1	-
ENSDART00000184891.1	nlgn3a-206	3307	858aa	ENSDARP00000155907.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M9QB35	-
ENSDART00000180112.1	nlgn3a-204	3307	858aa	ENSDARP00000157490.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSDART00000168320.2	nlgn3a-201	2754	878aa	ENSDARP00000134245.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IJ74	-
ENSDART00000182488.1	nlgn3a-205	2448	815aa	ENSDARP00000156469.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D0EVX1	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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