TGFB1 Chromosome 19
Transforming growth factor beta 1
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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
RS199758510
Conflicting classifications of pathogenicity
Health Risk
RS200164212
Conflicting classifications of pathogenicity
Health Risk
RS200482214
Conflicting classifications of pathogenicity
TGFB1-related disorder, TGFB1-related disorder
Health Risk
RS72480429
Conflicting classifications of pathogenicity
Health Risk
RS765327656
Conflicting classifications of pathogenicity
Diaphyseal dysplasia, Cystic fibrosis, Inflammatory bowel disease
Health Risk
RS779534698
Conflicting classifications of pathogenicity
Health Risk
RS1057521741
Likely pathogenic
Health Risk
RS1336387628
Likely pathogenic
Encephalopathy, IL10-related early-onset inflammatory bowel disease, Inflammatory bowel disease
Health Risk
RS1555755242
Likely pathogenic
Inflammatory bowel disease, immunodeficiency, and encephalopathy
Health Risk
RS1555755308
Likely pathogenic
Encephalopathy, IL10-related early-onset inflammatory bowel disease, Inflammatory bowel disease
Health Risk
RS1599893542
Likely pathogenic
Diaphyseal dysplasia, Diaphyseal dysplasia
Health Risk
RS2513384226
Likely pathogenic
Inflammatory bowel disease, immunodeficiency, and encephalopathy
Health Risk
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 |