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Spermatogenesis-defective protein 39 homolog (VIPAS39)

Homo sapiens — UniProt Q9H9C1

Gene: VIPAS39Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Spermatogenesis-defective protein 39 homolog (VIPAS39) is a protein from Homo sapiens identified by UniProt accession Q9H9C1, 493 residues long. MolForge cross-references it against 0 known binders and 21 disease associations.

  • UniProt accession: Q9H9C1; gene symbol VIPAS39.
  • Organism: Homo sapiens.
  • Length: 493 amino acids.
  • Top disease associations (Open Targets): Arthrogryposis - renal dysfunction - cholestasis, arthrogryposis-renal dysfunction-cholestasis syndrome and arthrogryposis.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSpermatogenesis-defective protein 39 homolog
UniProt accessionQ9H9C1
GeneVIPAS39
OrganismHomo sapiens
Length493 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 (21)

Diseases linked to this target (Open Targets).

  • Arthrogryposis - renal dysfunction - cholestasis · score 0.80
  • arthrogryposis-renal dysfunction-cholestasis syndrome · score 0.59
  • arthrogryposis · score 0.46
  • genetic disorder · score 0.19
  • leukocyte count · score 0.14
  • neutrophil count · score 0.11
  • apolipoprotein A 1 measurement · score 0.11
  • lymphocyte percentage of leukocytes · score 0.10
  • protein measurement · score 0.09
  • sum of neutrophil and eosinophil counts · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H9C1-F1alphafoldPREDICTED78.14—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H9C1.

Amino-acid sequence (493 residues)

MNRTKGDEEE YWNSSKFKAF TFDDEDDELS QLKESKRAVN SLRDFVDDDD DDDLERVSWS GEPVGSISWS IRETAGNSGS THEGREQLKS RNSFSSYAQL PKPTSTYSLS SFFRGRTRPG SFQSLSDALS DTPAKSYAPE LGRPKGEYRD YSNDWSPSDT VRRLRKGKVC SLERFRSLQD KLQLLEEAVS MHDGNVITAV LIFLKRTLSK EILFRELEVR QVALRHLIHF LKEIGDQKLL LDLFRFLDRT EELALSHYRE HLNIQDPDKR KEFLKTCVGL PFSAEDSAHI QDHYTLLERQ IIIEANDRHL ESAGQTEIFR KHPRKASILN MPLVTTLFYS CFYHYTEAEG TFSSPVNLKK TFKIPDKQYV LTALAARAKL RAWNDVDALF TTKNWLGYTK KRAPIGFHRV VEILHKNNAP VQILQEYVNL VEDVDTKLNL ATKFKCHDVV IDTYRDLKDR QQLLAYRSKV DKGSAEEEKI DALLSSSQIR WKN

Frequently asked questions

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

Which diseases are associated with VIPAS39?

The strongest Open Targets associations for VIPAS39 are Arthrogryposis - renal dysfunction - cholestasis, arthrogryposis-renal dysfunction-cholestasis syndrome, arthrogryposis, genetic disorder and leukocyte count.

How long is the VIPAS39 protein?

The Homo sapiens VIPAS39 protein (UniProt Q9H9C1) is 493 amino acids long.

Browse: Targets: V · 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

UniProtQ9H9C1
GeneVIPAS39
OrganismHomo sapiens
Length493
Binders0
Diseases21
View on UniProt