Human (GRCh38.p14)
Description

solute carrier organic anion transporter family member 1B3 [Source:HGNC Symbol;Acc:HGNC:10961]

Gene Synonyms

OATP1B3, OATP8, SLC21A8

Location
About this transcript

This transcript has 16 exons, is annotated with 50 domains and features, is associated with 52234 variant alleles and maps to 545 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000381545.8SLCO1B3-2023013702aaENSP00000370956.4
 
Protein coding
CCDS8684Q9NPD5-1 NM_019844.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:2
ENST00000261196.6SLCO1B3-2012840702aaENSP00000261196.2
 
Protein coding
CCDS8684Q9NPD5-1 -GENCODE BasicAPPRIS P1TSL:1
ENST00000901223.1SLCO1B3-2072779702aaENSP00000571282.1
 
Protein coding
CCDS8684--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000901222.1SLCO1B3-2062744702aaENSP00000571281.1
 
Protein coding
CCDS8684--GENCODE BasicAPPRIS P1
ENST00000901224.1SLCO1B3-2082293566aaENSP00000571283.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000544370.1SLCO1B3-2041771479aaENSP00000443225.1
 
Protein coding
H0YGG9 -TSL:5CDS 5' incomplete
ENST00000540853.5SLCO1B3-2031002291aaENSP00000442000.1
 
Protein coding
F5H8K0 -TSL:1CDS 3' incomplete
ENST00000545880.1SLCO1B3-205339No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 16, Coding exons: 14, Transcript length: 3,013 bps, Translation length: 702 residues

MANE

This MANE Select transcript contains ENSP00000370956 and matches to NM_019844.4 and NP_062818.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NPD5

CCDS

This transcript is a member of the Human CCDS set: CCDS8684

Transcript Support Level (TSL)

TSL:2

Version

ENST00000381545.8

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

upstream ATG [Definitions]

GENCODE basic gene

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

GENCODE primary gene

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