Transcript: ENSRNOT00000058382.5 Nfatc1-201

Description

nuclear factor of activated T-cells 1 [Source:RGD Symbol;Acc:2319357]

Gene Synonyms

LOC100361818

Location

About this transcript

This transcript has 10 exons, is annotated with 22 domains and features, is associated with 354 variant alleles and maps to 168 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000058382.5	Nfatc1-201	4425	939aa	ENSRNOP00000055183.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZE20	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 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,
ENSRNOT00000090369.2	Nfatc1-202	4141	925aa	ENSRNOP00000070317.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXL2	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,

Summary

Statistics

Exons: 10, Coding exons: 10, Transcript length: 4,425 bps, Translation length: 939 residues

Version

ENSRNOT00000058382.5

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.