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SLC25A12


Official Full Name
solute carrier family 25 member 12
Organism
Homo sapiens
Gene ID
8604
Background
This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]
Synonyms
AGC1; DEE39; ARALAR; EIEE39

Cat.No. Product Name Price
SHH409416 shRNA set against Human SLC25A12 (NM_003705.4) Inquiry
SHH409420 shRNA set against Mouse SLC25A12 (NM_172436.3) Inquiry
SHW017936 shRNA set against Danio rerio SLC25A12 (NM_212782) Inquiry
Cat.No. Product Name Price
CDCR270985 Mouse Slc25a12 ORF Clone(NM_172436.3) Inquiry
MiUTR1M-10798 SLC25A12 miRNA 3'UTR clone Inquiry
MiUTR3H-06169 SLC25A12 miRNA 3'UTR clone Inquiry
CDCB179411 Danio rerio SLC25A12 ORF Clone (NM_212782) Inquiry
CDCB187693 Rabbit SLC25A12 ORF clone (XM_008258912.1) Inquiry
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