ABCA12

protein
Name=ATP-binding cassette, sub-family A (ABC1), member 12
caption=


width=
HGNCid=14637
Symbol=ABCA12
AltSymbols=
EntrezGene=26154
OMIM=607800
RefSeq=NM_173076
UniProt=Q86UK0
PDB=
ECnumber=
Chromosome=2
Arm=q
Band=35
LocusSupplementaryData=

ABCA12 (ATP-binding cassette, sub-family A (ABC1), member 12) is a gene that belongs to a group of genes called the ATP-binding cassette family, which makes proteins that transport molecules across cell membranes. The ABCA12 gene is active in some types of skin cells and in several other tissues, such as testis, placenta, lung, stomach, and fetal brain and liver. The ABCA12 protein appears to be essential for normal development of the skin, which provides a barrier between the body and its surrounding environment. Although the exact function of the protein is unknown, researchers suggest that it probably plays an important role in transporting lipids (fats) in cells that make up the outermost layer of skin (the epidermis).

The ABCA12 gene is located on the long (q) arm of chromosome 2 between positions 34 and 35, from base pair 215,621,772 to base pair 215,828,656.

Related conditions

Several mutations in the ABCA12 gene are known to cause harlequin ichthyosis. Most of these mutations are predicted to lead to an absence of ABCA12 protein or the production of an extremely small version of the protein that cannot transport lipids properly. A loss of functional ABCA12 protein causes numerous problems with the development of the epidermis before and after birth. Abnormalities in lipid transport prevent the skin from forming an effective barrier and result in the hard, thick scales characteristic of harlequin ichthyosis.

Mutations in the ABCA12 gene also cause another severe skin disorder, lamellar ichthyosis type 2. People with this disorder have red, scaly, plate-like skin covering most of their bodies. The ABCA12 mutations that cause this disorder substitute one amino acid (a building block of proteins) for another amino acid in the ABCA12 protein. These mutations almost always occur in an important functional region of the protein (the region that binds to ATP, a molecule that supplies energy for chemical reactions). Changes in the structure of the ABCA12 protein likely disrupt its ability to transport lipids, which affects the development of skin before and after birth.

References

* PMID 12697999
* PMID 15756637 [http://www.pubmedcentral.gov/articlerender.fcgi?tool=pubmed&pubmedid=15756637 "Full text"]
* PMID 12915478

External links

* [http://www.genecards.org/cgi-bin/carddisp?ABCA12 GeneCard]
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