Transcript: ENST00000311856.9 SLC22A13-201

Description

solute carrier family 22 member 13 [Source:HGNC Symbol;Acc:HGNC:8494]

Gene Synonyms

OAT10, OCTL1, OCTL3, ORCTL3

Location

Chromosome 3: 38,265,812-38,278,757 forward strand.

About this transcript

This transcript has 10 exons, is annotated with 20 domains and features, is associated with 5802 variant alleles and maps to 484 oligo probes.

Gene

This transcript is a product of gene ENSG00000172940.13 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000311856.9	SLC22A13-201	2997	551aa	ENSP00000310241.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS2676	Q9Y226-1	NM_004256.4	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000649621.1	SLC22A13-203	1685	130aa	ENSP00000497644.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A3B3ITC0	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000415844.1	SLC22A13-202	1079	231aa	ENSP00000395106.1	Nonsense mediated decay		H0Y4Y1	-	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:2, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

Summary

Statistics

Exons: 10, Coding exons: 10, Transcript length: 2,997 bps, Translation length: 551 residues

MANE

This MANE Select transcript contains ENSP00000310241 and matches to NM_004256.4 and NP_004247.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y226

CCDS

This transcript is a member of the Human CCDS set: CCDS2676

Transcript Support Level (TSL)

TSL:1

Version

ENST00000311856.9

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript: ENST00000311856.9 SLC22A13-201

Summary

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Transcript: ENST00000311856.9 SLC22A13-201

Summary

About Us

Get help

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