RecName: Full=Molybdenum cofactor sulfurase; Short=MCS; Short=MOS; Sho - Protein

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The rs594445 in MOCOS gene is associated with risk of autism spectrum disorder. [Metab Brain Dis. 2020]
The rs594445 in MOCOS gene is associated with risk of autism spectrum disorder.
Taheri M, Noroozi R, Aghaei K, Omrani MD, Ghafouri-Fard S. Metab Brain Dis. 2020 Mar; 35(3):497-501. Epub 2020 Jan 4.
Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria. [Cell Physiol Biochem. 2015]
Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
Zhou Y, Zhang X, Ding R, Li Z, Hong Q, Wang Y, Zheng W, Geng X, Fan M, Cai G, et al. Cell Physiol Biochem. 2015; 35(6):2412-21. Epub 2015 Apr 24.
Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria. [Mol Genet Metab. 2007]
Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria.
Peretz H, Naamati MS, Levartovsky D, Lagziel A, Shani E, Horn I, Shalev H, Landau D. Mol Genet Metab. 2007 May; 91(1):23-9. Epub 2007 Mar 23.

RefSeq genomic sequence
See the genomic reference sequence for the MOCOS gene (NG_053177.2).
RefSeq protein
See the reference protein sequence for molybdenum cofactor sulfurase (NP_060417.4).

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Transcript/Protein Information [PANTHER Classification System]
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Protein