Version 5.4
| Mus musculus Gene: Slc25a19 | |||||||||
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| Summary | |||||||||
| InnateDB Gene | IDBG-214336.6 | ||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||
| Gene Symbol | Slc25a19 | ||||||||
| Gene Name | solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 | ||||||||
| Synonyms | 2900089E13Rik; DNC; MUP1; TPC | ||||||||
| Species | Mus musculus | ||||||||
| Ensembl Gene | ENSMUSG00000020744 | ||||||||
| Encoded Proteins |
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
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| Protein Structure |
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| Useful resources | Stemformatics EHFPI ImmGen | ||||||||
| Entrez Gene | |||||||||
| Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000125454:
This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008] |
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| Gene Information | |||||||||
| Type | Protein coding | ||||||||
| Genomic Location | Chromosome 11:115614178-115628295 | ||||||||
| Strand | Reverse strand | ||||||||
| Band | E2 | ||||||||
| Transcripts | |||||||||
| Interactions | |||||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
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| Gene Ontology | |||||||||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Orthologs | |||||||||
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Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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| Cross-References | |||||||||
| SwissProt | Q9DAM5 | ||||||||
| TrEMBL | A2A9V3 A2A9V4 | ||||||||
| UniProt Splice Variant | |||||||||
| Entrez Gene | 67283 | ||||||||
| UniGene | |||||||||
| RefSeq | NM_026071 XM_006533980 NM_001252384 NM_001252394 XM_006533979 | ||||||||
| OMIM | |||||||||
| CCDS | CCDS25644 CCDS56819 | ||||||||
| HPRD | |||||||||
| IMGT | |||||||||
| MGI ID | MGI:1914533 | ||||||||
| MGI Symbol | Slc25a19 | ||||||||
| EMBL | AK005710 AK172622 AL645470 AL732491 BC018167 | ||||||||
| GenPept | AAH18167 BAB24199 BAE43100 CAM22998 | ||||||||
| RNA Seq Atlas | 67283 | ||||||||