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3 beta-hydroxysteroid dehydrogenase type 7 (HSD3B7)

Homo sapiens — UniProt Q9H2F3

Gene: HSD3B7Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

3 beta-hydroxysteroid dehydrogenase type 7 (HSD3B7) is a protein from Homo sapiens identified by UniProt accession Q9H2F3, 369 residues long. MolForge cross-references it against 0 known binders and 113 disease associations.

  • UniProt accession: Q9H2F3; gene symbol HSD3B7.
  • Organism: Homo sapiens.
  • Length: 369 amino acids.
  • Top disease associations (Open Targets): congenital bile acid synthesis defect 1, Congenital bile acid synthesis defect type 1 and mean corpuscular volume.
  • 3D structure: AlphaFold model available.

Target properties

Protein name3 beta-hydroxysteroid dehydrogenase type 7
UniProt accessionQ9H2F3
GeneHSD3B7
OrganismHomo sapiens
Length369 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (113)

Diseases linked to this target (Open Targets).

  • congenital bile acid synthesis defect 1 · score 0.73
  • Congenital bile acid synthesis defect type 1 · score 0.72
  • mean corpuscular volume · score 0.32
  • erythrocyte count · score 0.28
  • mean corpuscular hemoglobin concentration · score 0.25
  • vital capacity · score 0.25
  • mean reticulocyte volume · score 0.23
  • Immature Reticulocyte Fraction Measurement · score 0.23
  • neuroticism measurement · score 0.20
  • mean corpuscular hemoglobin · score 0.19

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H2F3-F1alphafoldPREDICTED93.78—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H2F3.

Amino-acid sequence (369 residues)

MADSAQAQKL VYLVTGGCGF LGEHVVRMLL QREPRLGELR VFDQHLGPWL EELKTGPVRV TAIQGDVTQA HEVAAAVAGA HVVIHTAGLV DVFGRASPKT IHEVNVQGTR NVIEACVQTG TRFLVYTSSM EVVGPNTKGH PFYRGNEDTP YEAVHRHPYP CSKALAEWLV LEANGRKVRG GLPLVTCALR PTGIYGEGHQ IMRDFYRQGL RLGGWLFRAI PASVEHGRVY VGNVAWMHVL AARELEQRAT LMGGQVYFCY DGSPYRSYED FNMEFLGPCG LRLVGARPLL PYWLLVFLAA LNALLQWLLR PLVLYAPLLN PYTLAVANTT FTVSTDKAQR HFGYEPLFSW EDSRTRTILW VQAATGSAQ

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with HSD3B7?

The strongest Open Targets associations for HSD3B7 are congenital bile acid synthesis defect 1, Congenital bile acid synthesis defect type 1, mean corpuscular volume, erythrocyte count and mean corpuscular hemoglobin concentration.

How long is the HSD3B7 protein?

The Homo sapiens HSD3B7 protein (UniProt Q9H2F3) is 369 amino acids long.

Browse: Targets: H · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ9H2F3
GeneHSD3B7
OrganismHomo sapiens
Length369
Binders0
Diseases113
View on UniProt