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TGFB2

Chr 1q41

transforming growth factor beta 2

MANE:
ENST00000366930.9

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Arthrogryposis

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • DDG2P

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Ehlers Danlos syndrome with a likely monogenic cause

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Fetal anomalies

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Pneumothorax - familial

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Skeletal dysplasia

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Thoracic aortic aneurysm or dissection

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Thoracic aortic aneurysm or dissection (GMS)

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

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Disease associations (Open Targets)

  • familial thoracic aortic aneurysm and aortic dissection

    0.77
  • Loeys-Dietz syndrome 4

    0.76
  • Loeys-Dietz syndrome

    0.74
  • myelodysplastic syndrome

    0.56
  • anemia

    0.53
  • Rare disease with thoracic aortic aneurysm and aortic dissection

    0.53
  • atrial fibrillation

    0.49
  • anemia (phenotype)

    0.48
  • Familial hemophagocytic lymphohistiocytosis

    0.48
  • Beta-thalassemia

    0.48

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Transforming growth factor beta-2 proprotein

Precursor of the Latency-associated peptide (LAP) and Transforming growth factor beta-2 (TGF-beta-2) chains, which constitute the regulatory and active subunit of TGF-beta-2, respectively

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.