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: NFATC2 ENSDARG00000100927

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Description

nuclear factor of activated T cells 2 [Source:HGNC Symbol;Acc:HGNC:7776]

Location

Chromosome 23: 39,089,574-39,164,866 forward strand.

GRCz11:CM002907.2

About this gene

This gene has 1 transcript (splice variant), 208 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000164711.2	NFATC2-201	2685	894aa	ENSDARP00000138593.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F9Z5	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,

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Summary

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