ABCC13

Putative ATP-binding cassette transporter sub-family C member 13 is a protein that is not present in humans. In humans, ABCC13 is a pseudogene.^[3]

ABCC13
Identifiers
Aliases	ABCC13, C21orf73, PRED6, ABCC13P, ATP binding cassette subfamily C member 13 (pseudogene)
External IDs	OMIM: 608835; GeneCards: ABCC13; OMA:ABCC13 - orthologs
Gene location (Human) Chr. Chromosome 21 (human)[1] Band 21q11.2 Start 14,236,206 bp[1] End 14,362,754 bp[1]
Orthologs Species Human Mouse Entrez 150000 n/a Ensembl ENSG00000243064 n/a UniProt n a n/a RefSeq (mRNA) NM_138726 NM_172024 NM_172025 NM_172026 n/a RefSeq (protein) n/a n/a Location (UCSC) Chr 21: 14.24 – 14.36 Mb n/a PubMed search [2] n/a
Wikidata
View/Edit Human

Function

This gene is a member of the superfamily of genes encoding 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, and White). This family member is part of the MRP subfamily, which is involved in multi-drug resistance, but the human locus is now thought to be a pseudogene incapable of encoding a functional ABC protein. Alternative splicing results in multiple transcript variants; however, not all variants have been fully described.^[3]

See also

• ATP-binding cassette transporter
• ABCC13+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)