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

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Gene: NCAM2 ENSSSCG00000012020

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Description

neural cell adhesion molecule 2 [Source:VGNC Symbol;Acc:VGNC:90595]

Location

Primary_assembly 13: 185,176,461-185,679,885 forward strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 3 transcripts (splice variants), 214 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000099960.1	NCAM2-203	8308	912aa	ENSSSCP00000079027.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FL51	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSSSCT00000090466.2	NCAM2-202	7875	834aa	ENSSSCP00000073656.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R9A7	-
ENSSSCT00000013151.4	NCAM2-201	7872	833aa	ENSSSCP00000012802.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1GKA4 F1SHP7	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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