Human (GRCh38.p14)
Description

ATP binding cassette subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:57]

Gene Synonyms

ARA, EST349056, MLP1, MRP6, PXE, URG7

Location

Chromosome 16: 16,149,565-16,223,522 reverse strand.

GRCh38:CM000678.2

View alleles of this gene on alternative sequences

About this gene

This gene has 8 transcripts (splice variants), 1 gene allele, 166 orthologues, 11 paralogues and is associated with 7 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000205557.12ABCC6-20151401503aaENSP00000205557.7
 
Protein coding
CCDS10568O95255-1 NM_001171.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000574094.6ABCC6-2031517467aaENSP00000507301.1
 
Protein coding
A0A804HJ04 -GENCODE basicTSL:5
ENST00000575728.1ABCC6-20471499aaENSP00000461686.1
 
Protein coding
CCDS58430O95255-2 -GENCODE basicTSL:1
ENST00000622290.5ABCC6-20852031296aaENSP00000483331.2
 
Nonsense mediated decay
A0A8C8Q0G8 -TSL:5
ENST00000456970.6ABCC6-2024137871aaENSP00000405002.2
 
Nonsense mediated decay
O95255-3 -TSL:2
ENST00000577103.1ABCC6-207138182aaENSP00000459243.1
 
Nonsense mediated decay
I3L1Z6 -TSL:5
ENST00000576204.6ABCC6-205969No protein-
 
Retained intron
--TSL:5
ENST00000576683.1ABCC6-206476No protein-
 
Retained intron
--TSL:3