Citrin
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| solute carrier family 25, member 13 (citrin) | |
|---|---|
| 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
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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