ABCC6 ATP binding cassette subfamily C member 6
Gene ID: 368, updated on 4-Jan-2025Gene type: protein coding
Also known as: ARA; PXE; MLP1; MRP6; PXE1; URG7; ABC34; GACI2; MOATE; MOAT-E; EST349056
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- Go to complete Gene record for ABCC6
- Go to Variation Viewer for ABCC6 variants
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). The encoded protein, a member of the MRP subfamily, is involved in multi-drug resistance. Mutations in this gene cause pseudoxanthoma elasticum. Alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Jul 2008]
Associated conditions
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Description | Tests |
---|---|
Arterial calcification, generalized, of infancy, 2 | See labs |
Autosomal recessive inherited pseudoxanthoma elasticum | See labs |
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. GeneReviews: Not available | |
Pseudoxanthoma elasticum, forme fruste | See labs |
Genomic context
- Location:
- 16p13.11
- Sequence:
- Chromosome: 16; NC_000016.10 (16149565..16223494, complement)
- Total number of exons:
- 31
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for ABCC6 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ABCC6 @ LOVD
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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