ClinGen Knowledge Base | Clinical Genome Resource

MOCS2

Name: MOCS2
HGNC ID: HGNC:7193
Cytogenetic Location: 5q11.2
Haploinsufficiency: Associated with Autosomal Recessive Phenotype

External Resources: View external resources
ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

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	05/31/2017	View report

MOCS2

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype	05/31/2017	View report

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.