Transcript: ENSRNOT00000095294.1 Radil-202

Description

Rap associating with DIL domain [Source:RGD Symbol;Acc:1306155]

Gene Synonyms

LOC304299, RGD1306155

Location

About this transcript

This transcript has 15 exons, is annotated with 27 domains and features, is associated with 203 variant alleles and maps to 204 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095294.1	Radil-202	3612	1100aa	ENSRNOP00000083450.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZWZ1	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,
ENSRNOT00000033998.5	Radil-201	3756	1094aa	ENSRNOP00000033795.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A1Z8	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: 15, Coding exons: 15, Transcript length: 3,612 bps, Translation length: 1,100 residues

Version

ENSRNOT00000095294.1

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.