GDF1 Chromosome 19

Growth differentiation factor 1
28 variants 28 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 each subunit of the disulfide-linked homodimer. Studies in rodents suggest that this protein is involved in the establishment of left-right asymmetry in early embryogenesis and in neural development in later embryogenesis. The encoded protein is translated from a bicistronic mRNA that also encodes ceramide synthase 1. Mutations in this gene are associated with several congenital cardiovascular malformations. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
Transforming growth factor beta superfamily
Locus Type
gene with protein product
Location
19p13.11
Ensembl
ENSG00000130283
Associated Conditions (11)
Tetralogy of Fallot
GDF1-related disorder
Inborn genetic diseases
Right atrial isomerism
Congenital heart defects
multiple types
6
Visceral heterotaxy
Heterotaxy
Heart
malformation of
Key Variants
All Variants (28)
RSID Category Clinical Significance Conditions
RS121434424 Health Risk Conflicting classifications of pathogenicity Tetralogy of Fallot, GDF1-related disorder, Tetralogy of Fallot
RS1417119878 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS370986101 Health Risk Conflicting classifications of pathogenicity
RS765449212 Health Risk Conflicting classifications of pathogenicity
RS864622513 Health Risk Conflicting classifications of pathogenicity GDF1-related disorder, GDF1-related disorder
RS944730356 Health Risk Conflicting classifications of pathogenicity
RS1057524707 Health Risk Likely pathogenic
RS1064793136 Health Risk Likely pathogenic
RS1064793138 Health Risk Likely pathogenic
RS1555702261 Health Risk Likely pathogenic Right atrial isomerism, Right atrial isomerism
RS2055908725 Health Risk Likely pathogenic
RS2145983859 Health Risk Likely pathogenic
RS2512952981 Health Risk Likely pathogenic
RS900625437 Health Risk Likely pathogenic Congenital heart defects, multiple types, 6
RS1009289636 Health Risk Pathogenic
RS1213194580 Health Risk Pathogenic
RS1466604623 Health Risk Pathogenic
RS1487660277 Health Risk Pathogenic
RS1601143502 Health Risk Pathogenic Visceral heterotaxy, Visceral heterotaxy
RS2055909070 Health Risk Pathogenic
RS2055936732 Health Risk Pathogenic
RS2145989089 Health Risk Pathogenic
RS753643819 Health Risk Pathogenic Right atrial isomerism, Right atrial isomerism
RS938987727 Health Risk Pathogenic
RS1359321518 Health Risk Pathogenic/Likely pathogenic Inborn genetic diseases, Heterotaxy, Right atrial isomerism
RS374016704 Health Risk Pathogenic/Likely pathogenic Congenital heart defects, multiple types, 6
RS606231383 Health Risk Pathogenic/Likely pathogenic Right atrial isomerism, Congenital heart defects, multiple types
RS768027510 Health Risk Pathogenic/Likely pathogenic Congenital heart defects, multiple types, 6
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