| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGGCAGGCCAGGAACGCACGCUGCCUGGCCGUAUCGCCGCCCCCACCGC… | 3144 nt | 0.4437 | |
| AGGCAGGCCAGGAACGCACGCUGCCUGGCCGUAUCGCCGCCCCCACCGC… | 3141 nt | 0.4435 |
This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
A study in mice demonstrated that the SLC25A13 transcript, a calcium-binding mitochondrial carrier protein, increased in abundance within 0.5 hours postmortem [Pozhitkov et al. DOI:10.1098/rsob.160267]. This transcript, categorized as a transport gene, was part of a broader finding where 1063 gene transcripts showed significant, time-dependent increases after death, suggesting a step-wise shutdown process with potential for postmortem interval estimation.