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: NFATC3 ENSBTAG00000004368

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Description

nuclear factor of activated T cells 3 [Source:VGNC Symbol;Acc:VGNC:32033]

Location

Primary_assembly 18: 35,517,901-35,609,581 forward strand.

ARS-UCD1.3:CM008185.2

About this gene

This gene has 4 transcripts (splice variants), 210 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000131212.1	NFATC3-204	3852	1075aa	ENSBTAP00000101701.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000005727.7	NFATC3-202	3846	1073aa	ENSBTAP00000005727.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MSU2	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,
ENSBTAT00000105772.1	NFATC3-203	3676	1062aa	ENSBTAP00000094196.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000074076.2	NFATC3-201	3403	1066aa	ENSBTAP00000063040.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LRX2	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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Summary

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