AMH Chromosome 19

Anti-Mullerian hormone
22 variants 22 Health Risk

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What This Gene Does
This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate N- and C-terminal cleavage products that homodimerize and associate to form a biologically active noncovalent complex. This complex binds to the anti-Mullerian hormone receptor type 2 and causes the regression of Mullerian ducts in the male embryo that would otherwise differentiate into the uterus and fallopian tubes. This protein also plays a role in Leydig cell differentiation and function and follicular development in adult females. Mutations in this gene result in persistent Mullerian duct syndrome. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
"Receptor ligands|MicroRNA protein coding host genes|Transforming growth factor beta superfamily"
Locus Type
gene with protein product
Location
19p13.3
Ensembl
ENSG00000104899
Associated Conditions (6)
Persistent Mullerian duct syndrome
AMH-related disorder
Inborn genetic diseases
Genetic non-acquired premature ovarian failure
Persistent mullerian duct syndrome
type I
Key Variants
All Variants (22)
RSID Category Clinical Significance Conditions
RS199831511 Health Risk Conflicting classifications of pathogenicity Persistent Mullerian duct syndrome, Persistent Mullerian duct syndrome
RS374588581 Health Risk Conflicting classifications of pathogenicity
RS536688211 Health Risk Conflicting classifications of pathogenicity AMH-related disorder, AMH-related disorder
RS556078854 Health Risk Conflicting classifications of pathogenicity
RS566806768 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, AMH-related disorder, Inborn genetic diseases
RS566876047 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS767665662 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1012178126 Health Risk Likely pathogenic
RS2145032534 Health Risk Likely pathogenic Genetic non-acquired premature ovarian failure, Genetic non-acquired premature ovarian failure
RS2512014671 Health Risk Likely pathogenic Persistent Mullerian duct syndrome, Persistent Mullerian duct syndrome
RS104894666 Health Risk Pathogenic Persistent mullerian duct syndrome, type I, Persistent Mullerian duct syndrome
RS1183532981 Health Risk Pathogenic Persistent Mullerian duct syndrome, Persistent Mullerian duct syndrome
RS1443929462 Health Risk Pathogenic Persistent Mullerian duct syndrome, Persistent Mullerian duct syndrome
RS1461776340 Health Risk Pathogenic
RS2025018868 Health Risk Pathogenic Persistent Mullerian duct syndrome, Persistent Mullerian duct syndrome
RS267606654 Health Risk Pathogenic Persistent mullerian duct syndrome, type I, Persistent mullerian duct syndrome
RS371874189 Health Risk Pathogenic
RS397518444 Health Risk Pathogenic Persistent mullerian duct syndrome, type I, Persistent mullerian duct syndrome
RS769922506 Health Risk Pathogenic
RS774430982 Health Risk Pathogenic
RS774592796 Health Risk Pathogenic Persistent mullerian duct syndrome, type I, Persistent mullerian duct syndrome
RS1415701260 Health Risk Pathogenic/Likely pathogenic Persistent Mullerian duct syndrome, Persistent Mullerian duct syndrome
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