Transcript: ENSRNOT00000064863.4 Skint1-201

Description

selection and upkeep of intraepithelial T cells 1 [Source:RGD Symbol;Acc:1587579]

Gene Synonyms

LOC689801

Location

About this transcript

This transcript has 8 exons, is annotated with 24 domains and features, is associated with 334 variant alleles and maps to 60 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000064863.4	Skint1-201	1201	377aa	ENSRNOP00000060977.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2ZEZ3	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,
ENSRNOT00000087012.3	Skint1-202	937	289aa	ENSRNOP00000075376.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2KAF2	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: 8, Coding exons: 7, Transcript length: 1,201 bps, Translation length: 377 residues

Version

ENSRNOT00000064863.4

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.