" /> SLC16A2 wt Allele - CISMeF





Preferred Label : SLC16A2 wt Allele;

NCIt synonyms : DXS128E; AHDS; Solute Carrier Family 16, Member 2 (Monocarboxylic Acid Transporter 8) Gene; MCT7; MCT8; Solute Carrier Family 16 Member 2 wt Allele; Mental Retardation, X-Linked 22 Gene; Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 2 Gene; Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 2 (Putative Transporter) Gene; Solute Carrier Family 16, Member 2 (Thyroid Hormone Transporter) Gene; Allan-Herndon-Dudley Syndrome Gene; MRX22; MCT 7; MCT 8; DXS128; Solute Carrier Family 16 (Monocarboxylic Acid Transporter), Member 2 Gene; XPCT;

NCIt definition : Human SLC16A2 wild-type allele is located in the vicinity of Xq13.2 and is approximately 112 kb in length. This allele, which encodes monocarboxylate transporter 8 protein, plays a role in cell uptake of thyroid hormone. Mutations in the gene are associated with Allan-Herndon-Dudley syndrome.;

NCI Metathesaurus CUI : CL1799117;

GenBank Accession Number : NM_006517;

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12/05/2024


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