Regulating Pair
       Introduced Variation Mutation (G558D) of SLC16A2 Protein Info
       Induced Change Liothyronine concentration: increase (FC = 2.3) Metabo Info
       Summary Introduced Variation         Induced Change 
Full List of Experiment(s) Validating This Regulating Pair
Details of Experiment for Validating This Pair [1]
       Method Quantifying the change of liothyronine concentration after SLC16A2 mutation (G558D) through kit detection.
       Disease Status Hypothyroidism ICD-11: 5A00
       Organ/Tissue/Cell Line COS-1 cells (Transformed african green monkey kidney fibroblast cells) N.A.
       Subcellular Location Membrane (Cell membrane)
       Tested Species   Species: Homo sapiens  (Click to Show/Hide the Complete Species Lineage)
Kingdom: Metazoa
Phylum: Chordata
Class: Mammalia
Order: Primates
Family: Hominidae
Genus: Homo
Species: Homo sapiens
       Details It is reported that mutation (G558D) of SLC16A2 leads to the increase of liothyronine levels compared with control group in COS-1 cells.
References
1 Mutations in MCT8 in patients with Allan-Herndon-Dudley-syndrome affecting its cellular distribution. Mol Endocrinol. 2013 May;27(5):801-13.

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