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Variant Pathogenicity
MOCS2
Name
MOCS2
HGNC ID
HGNC:7193
Cytogenetic Location
5q11.2
Haploinsufficiency
Associated with Autosomal Recessive Phenotype
Triplosensitivity
No Evidence
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ClinVar Variants
MOCS2
-
sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
| MONDO:0009644
Curated by
Classification
Date
Report
Gene Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
10/25/2018
View report
MOCS2
Curated by
Classification
Date
Report
Gene Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
10/25/2018
View report
Gene Dosage Sensitivity
No Evidence for Triplosensitivity
10/25/2018
View report
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