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Browse our slc25a13 Proteins (slc25a13)

Full name:
Solute Carrier Family 25, Member 13 (Citrin) Proteins (slc25a13)
On www.antibodies-online.com are 5 Solute Carrier Family 25, Member 13 (Citrin) (slc25a13) Proteins from 3 different suppliers available. Additionally we are shipping slc25a13 Antibodies (50) and slc25a13 Kits (4) and many more products for this protein. A total of 61 slc25a13 products are currently listed.
Synonyms:
AI785475, aralar, aralar1, ARALAR2, CITRIN, CTLN2, Ctrn, MGC69168, RGD1565889, slc25a13
list all proteins Gene Name GeneID UniProt
slc25a13 10165 Q9UJS0
Rat slc25a13 slc25a13 362322  
slc25a13 50799 Q9QXX4

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slc25a13 Proteins (slc25a13) by Origin

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Human Solute Carrier Family 25, Member 13 (Citrin) (slc25a13) interaction partners

  1. the present study reported on clinical and molecular investigations of an infant with NICCD, who was confirmed to be a compound heterozygote of the c.851_854del4 mutation and a novel large deletion c.1019_1177+893del in the SLC25A13 gene.

  2. The large deletion enriched the SLC25A13 mutation spectrum, and its identification supported the concept that cDNA cloning analysis, along with other molecular tools such as semiquantitative PCR, could provide valuable clues, facilitating the identification of obscure SLC25A13 deletions.

  3. Data indicate that the patient was a compound heterozygote carrying c.851_854delGTAT and IVS16ins3kb mutations of the mitochondrial carrier citrin protein (SLC25A13) gene, which were respectively inherited from his mother and father.

  4. This study aims to screen for five prevalent SLC25A13 mutations, to calculate the mutation carrier rate in Guangdong.

  5. we reviewed the English literature on mutations in the SLC25A13 gene, and its genotype-phenotype correlations to provide valuable insights into the molecular genetic background of citrullinemia (show ASS1 Proteins)--{REVIEW}

  6. Mutation screening of the SLC25A13 gene revealed the compound heterozygous mutations c.1081C>T (p.R361*) and c.74C>A (p. A25E) which confirmed the diagnosis of NICCD. The nonsense mutation c.1081C>T (p.R361*) is novel.

  7. Point mutation of ASS1 (show ASS1 Proteins), ASL (show ADSL Proteins) and SLC25A13 is associated with citrullinemia (show ASS1 Proteins).

  8. Identification of novel SLC25A13 gene mutations in East Asian patients with citrin deficiency.

  9. Analysis of the SLC25A13 gene sequence.

  10. Report frequency SLC25A13 mutations in the Thai population and estimate prevalence of citrin deficiency.

Mouse (Murine) Solute Carrier Family 25, Member 13 (Citrin) (slc25a13) interaction partners

  1. hepatic metabolite perturbations in citrin-mitochondrial glycerol-3-phosphate dehydrogenase (show GPD1 Proteins) double-knockout mice, a model of human citrin deficiency

  2. The results support the notion that glial cells have much lower AGC (show ACAN Proteins) levels and MAS (show MAS1 Proteins) activity than neurons

  3. Expression of the aspartate/glutamate (show GRIN1 Proteins) mitochondrial carriers aralar1 (show Slc25a12 Proteins) and citrin during development(CITRIN)

  4. To investigate the physiological role of citrin and the development of CTLN2 (adult-onset type II citrullinemia (show ASS1 Proteins)), an Slc25a13-knockout mouse model was created.

  5. Aralar and citrin, when expressed as single isoforms in heart, confer differences in Ca(2 (show CA2 Proteins)+) activation of shuttle activity, probably associated with their structural differences.

  6. phenotypic analysis of citrin/mitochondrial glycerol-3-phosphate dehydrogenase (show GPD1 Proteins) double knock-out mice

slc25a13 Protein Profile

Protein Summary

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.

Alternative names and synonyms associated with slc25a13

  • solute carrier family 25 (aspartate/glutamate carrier), member 13 (SLC25A13)
  • solute carrier family 25, member 13 (citrin) (slc25a13)
  • solute carrier family 25, member 13 (citrin) (SLC25A13)
  • solute carrier family 25 (aspartate/glutamate carrier), member 12 (slc25a12)
  • solute carrier family 25 (aspartate/glutamate carrier), member 13 (slc25a13)
  • solute carrier family 25 (aspartate/glutamate carrier), member 13 (Slc25a13)
  • solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 (Slc25a13)
  • AI785475 protein
  • aralar protein
  • aralar1 protein
  • ARALAR2 protein
  • CITRIN protein
  • CTLN2 protein
  • Ctrn protein
  • MGC69168 protein
  • RGD1565889 protein
  • slc25a13 protein

Protein level used designations for slc25a13

solute carrier family 25, member 13 (citrin) , solute carrier family 25 (mitochondrial carrier, Aralar), member 12 , solute carrier family 25, member 12 , solute carrier family 25, member 13 , calcium-binding mitochondrial carrier protein Aralar2-like , calcium-binding mitochondrial carrier protein Aralar2 , mitochondrial aspartate glutamate carrier 2 , solute carrier family 25 (aspartate/glutamate carrier), member 13 tv2 , solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 , citrin , solute carrier family 25 member 13

GENE ID SPECIES
100063046 Equus caballus
398810 Xenopus laevis
472450 Pan troglodytes
549674 Xenopus (Silurana) tropicalis
699911 Macaca mulatta
100124779 Xenopus (Silurana) tropicalis
100401767 Callithrix jacchus
100434018 Pongo abelii
100466909 Ailuropoda melanoleuca
100561177 Anolis carolinensis
100606811 Nomascus leucogenys
10165 Homo sapiens
610138 Canis lupus familiaris
100524162 Sus scrofa
615470 Bos taurus
362322 Rattus norvegicus
50799 Mus musculus
428427 Gallus gallus
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