Transcript: ENSRNOT00000023896.8 Slc66a1-201

Description

solute carrier family 66 member 1 [Source:RGD Symbol;Acc:1311627]

Gene Synonyms

LOC362642, Pqlc2

Location

About this transcript

This transcript has 9 exons, is annotated with 15 domains and features, is associated with 58 variant alleles and maps to 118 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000023896.8	Slc66a1-201	1400	361aa	ENSRNOP00000023896.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QDE2	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,
ENSRNOT00000099105.1	Slc66a1-202	1568	310aa	ENSRNOP00000077592.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y800	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: 9, Coding exons: 7, Transcript length: 1,400 bps, Translation length: 361 residues

Version

ENSRNOT00000023896.8

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.