TGFB1 Chromosome 19

Transforming growth factor beta 1
17 variants 17 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 a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGFB family members. This encoded protein regulates cell proliferation, differentiation and growth, and can modulate expression and activation of other growth factors including interferon gamma and tumor necrosis factor alpha. This gene is frequently upregulated in tumor cells, and mutations in this gene result in Camurati-Engelmann disease. [provided by RefSeq, Aug 2016]
Gene Info
Gene Group
Transforming growth factor beta family
Locus Type
gene with protein product
Location
19q13.2
Ensembl
ENSG00000105329
Associated Conditions (11)
TGFB1-related disorder
Diaphyseal dysplasia
Cystic fibrosis
Inflammatory bowel disease
immunodeficiency
and encephalopathy
Encephalopathy
IL10-related early-onset inflammatory bowel disease
See cases
Inborn genetic diseases
CAMURATI-ENGELMANN DISEASE 1
Key Variants
All Variants (17)
RSID Category Clinical Significance Conditions
RS199758510 Health Risk Conflicting classifications of pathogenicity
RS200164212 Health Risk Conflicting classifications of pathogenicity
RS200482214 Health Risk Conflicting classifications of pathogenicity TGFB1-related disorder, TGFB1-related disorder
RS72480429 Health Risk Conflicting classifications of pathogenicity
RS765327656 Health Risk Conflicting classifications of pathogenicity Diaphyseal dysplasia, Cystic fibrosis, Inflammatory bowel disease
RS779534698 Health Risk Conflicting classifications of pathogenicity
RS1057521741 Health Risk Likely pathogenic
RS1336387628 Health Risk Likely pathogenic Encephalopathy, IL10-related early-onset inflammatory bowel disease, Inflammatory bowel disease
RS1555755242 Health Risk Likely pathogenic Inflammatory bowel disease, immunodeficiency, and encephalopathy
RS1555755308 Health Risk Likely pathogenic Encephalopathy, IL10-related early-onset inflammatory bowel disease, Inflammatory bowel disease
RS1599893542 Health Risk Likely pathogenic Diaphyseal dysplasia, Diaphyseal dysplasia
RS2513384226 Health Risk Likely pathogenic Inflammatory bowel disease, immunodeficiency, and encephalopathy
RS104894719 Health Risk Pathogenic Diaphyseal dysplasia, Diaphyseal dysplasia
RS104894721 Health Risk Pathogenic Diaphyseal dysplasia, See cases, Diaphyseal dysplasia
RS104894722 Health Risk Pathogenic Diaphyseal dysplasia, Diaphyseal dysplasia
RS111033611 Health Risk Pathogenic Diaphyseal dysplasia, Diaphyseal dysplasia
RS104894720 Health Risk Pathogenic/Likely pathogenic Diaphyseal dysplasia, Inborn genetic diseases, CAMURATI-ENGELMANN DISEASE 1
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