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

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Gene: NCR2 ENSNLEG00000004974

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Description

natural cytotoxicity triggering receptor 2 [Source:HGNC Symbol;Acc:HGNC:6732]

Location

Chromosome 17: 4,867,539-4,881,637 forward strand.

Nleu_3.0:CM001663.1

About this gene

This gene has 2 transcripts (splice variants), 61 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSNLET00000052888.1	NCR2-202	938	277aa	ENSNLEP00000047028.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3HTX9	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,
ENSNLET00000006343.3	NCR2-201	1081	271aa	ENSNLEP00000006030.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1QYK9	-

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Summary

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