Citrin
From Infogalactic: the planetary knowledge core
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solute carrier family 25, member 13 (citrin) | |
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Identifiers | |
Symbol | SLC25A13 |
Alt. symbols | CTLN2 |
Entrez | 10165 |
HUGO | 10983 |
OMIM | 603859 |
RefSeq | NM_014251 |
UniProt | Q9UJS0 |
Other data | |
Locus | Chr. 7 q21.3 |
Citrin also known as solute carrier family 25, member 13 (citrin) or SLC25A13 is a protein which in humans is encoded by the SLC25A13 gene.[1]
Citrin is associated with type II citrullinemia[2][3][4] and neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).
The term Citrin when referring to Vitamin-P was the most active Bio-flavonoid in lemons, it was found to be Eriodictyol (but a more active form constituent was found there decades later).
See also
References
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External links
- citrin at the US National Library of Medicine Medical Subject Headings (MeSH)
- GeneReviews/NCBI/NIH/UW entry on Citrin Deficiency
- SLC25A13 human gene location in the UCSC Genome Browser.
- SLC25A13 human gene details in the UCSC Genome Browser.
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