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: NFATC3 ENSSSCG00000029578

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Description

nuclear factor of activated T cells 3 [Source:VGNC Symbol;Acc:VGNC:90710]

Location

Primary_assembly 6: 28,666,549-28,806,419 forward strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 3 transcripts (splice variants), 212 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000048178.3	NFATC3-203	6078	1075aa	ENSSSCP00000051545.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B5I3 A0A4X1UG32	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSSSCT00000051936.3	NFATC3-201	6449	1042aa	ENSSSCP00000047112.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287ATC7	-
ENSSSCT00000062417.3	NFATC3-202	5962	1068aa	ENSSSCP00000056644.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BCI3 A0A4X1UD30	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data