Transcript: ENSRNOT00000039311.8 Ccdc66-201

Description

coiled-coil domain containing 66 [Source:RGD Symbol;Acc:1560873]

Gene Synonyms

LOC306238, RGD1560873

Location

About this transcript

This transcript has 18 exons, is annotated with 16 domains and features, is associated with 113 variant alleles and maps to 208 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000039311.8	Ccdc66-201	2994	945aa	ENSRNOP00000036334.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZB56	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,
ENSRNOT00000095208.1	Ccdc66-202	2985	912aa	ENSRNOP00000093577.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AK35	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: 18, Coding exons: 18, Transcript length: 2,994 bps, Translation length: 945 residues

Version

ENSRNOT00000039311.8

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.