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Human (GRCh38.p14)
Description

ATP binding cassette subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:42]

Gene Synonyms

ABC16, BSEP, PFIC-2, PFIC2, PGY4, SPGP

Location

Chromosome 2: 168,915,498-169,031,332 reverse strand.

GRCh38:CM000664.2

View alleles of this gene on alternative sequences

About this gene

This gene has 11 transcripts (splice variants), 1 gene allele, 217 orthologues, 10 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000650372.1ABCB11-20669341321aaENSP00000497931.1
 
Protein coding
CCDS46444O95342 NM_003742.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00001144143.1ABCB11-21176911321aaENSP00000815162.1
 
Protein coding
CCDS46444--Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00000858973.2ABCB11-20977331335aaENSP00000529032.1
 
Protein coding
--GENCODE Basic
ENST00000858972.2ABCB11-20875861286aaENSP00000529031.1
 
Protein coding
--GENCODE Basic
ENST00000858971.2ABCB11-20774241232aaENSP00000529030.1
 
Protein coding
--GENCODE Basic
ENST00000649448.1ABCB11-2052983780aaENSP00000497165.1
 
Protein coding
A0A3B3IS78 -CDS 5' incomplete
ENST00001106332.1ABCB11-21064935aaENSP00000776137.1
 
Protein coding
--GENCODE Basic
ENST00000648875.1ABCB11-204411101aaENSP00000497252.1
 
Protein coding
A0A3B3ISD4 -CDS 5' incomplete
ENST00000439188.1ABCB11-201282272aaENSP00000416058.1
 
Nonsense mediated decay
H7C486 -TSL:2CDS 5' incomplete
ENST00000647920.1ABCB11-20345281aaENSP00000497947.1
 
Nonsense mediated decay
A0A3B3ITV9 -CDS 5' incomplete
ENST00000478354.1ABCB11-202576No protein-
 
Retained intron
--TSL:4