Overview

Variant ID 19666
Entrez Gene ID 4363
Gene ABCC1 (GeneCards)
Location hg19 16:16080411-16080411
hg38 16:15986554-15986554
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000016.9:g.16080411 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 90354753

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1171
CADD Raw score (version 1.3) 0.657 (Deleterious)
FATHMM raw prediction score 0.1915 (Tolerated)
Deleterious probability by DeFine 0.1031 (Neutral)
Entrez Gene ID 4363 (NCBI Gene)
Official Gene Symbol ABCC1 (GeneCards)
Number of variants in ABCC1 in this database 2 (view all the variants)
Full name ATP binding cassette subfamily C member 1
Band 16p13.11
Other IDs Vega: OTTHUMG00000048267
OMIM: 158343
HGNC: HGNC:51
Ensembl: ENSG00000103222
Other names MRP, ABCC, GS-X, MRP1, ABC29
Summary The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra-and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This full transporter is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a multispecific organic anion transporter, with oxidized glutatione, cysteinyl leukotrienes, and activated aflatoxin B1 as substrates. This protein also transports glucuronides and sulfate conjugates of steroid hormones and bile salts. Alternatively spliced variants of this gene have been described but their full-length nature is unknown. [provided by RefSeq, Apr 2012]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;