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Spermatogenesis-associated protein 7 (SPATA7)

Homo sapiens — UniProt Q9P0W8

Gene: SPATA7Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Spermatogenesis-associated protein 7 (SPATA7) is a protein from Homo sapiens identified by UniProt accession Q9P0W8, 599 residues long. MolForge cross-references it against 0 known binders and 49 disease associations.

  • UniProt accession: Q9P0W8; gene symbol SPATA7.
  • Organism: Homo sapiens.
  • Length: 599 amino acids.
  • Top disease associations (Open Targets): Leber congenital amaurosis, retinitis pigmentosa and Retinal dystrophy.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSpermatogenesis-associated protein 7
UniProt accessionQ9P0W8
GeneSPATA7
OrganismHomo sapiens
Length599 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 (49)

Diseases linked to this target (Open Targets).

  • Leber congenital amaurosis · score 0.75
  • retinitis pigmentosa · score 0.60
  • Retinal dystrophy · score 0.51
  • retinitis pigmentosa 94, variable age at onset · score 0.50
  • severe early-childhood-onset retinal dystrophy · score 0.38
  • Posterior column ataxia - retinitis pigmentosa · score 0.37
  • creatinine measurement · score 0.35
  • glomerular filtration rate · score 0.35
  • autosomal recessive retinitis pigmentosa · score 0.33
  • Krabbe disease · score 0.27

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9P0W8-F1alphafoldPREDICTED57.52—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9P0W8.

Amino-acid sequence (599 residues)

MDGSRRVRAT SVLPRYGPPC LFKGHLSTKS NAFCTDSSSL RLSTLQLVKN HMAVHYNKIL SAKAAVDCSV PVSVSTSIKY ADQQRREKLK KELAQCEKEF KLTKTAMRAN YKNNSKSLFN TLQKPSGEPQ IEDDMLKEEM NGFSSFARSL VPSSERLHLS LHKSSKVITN GPEKNSSSSP SSVDYAASGP RKLSSGALYG RRPRSTFPNS HRFQLVISKA PSGDLLDKHS ELFSNKQLPF TPRTLKTEAK SFLSQYRYYT PAKRKKDFTD QRIEAETQTE LSFKSELGTA ETKNMTDSEM NIKQASNCVT YDAKEKIAPL PLEGHDSTWD EIKDDALQHS SPRAMCQYSL KPPSTRKIYS DEEELLYLSF IEDVTDEILK LGLFSNRFLE RLFERHIKQN KHLEEEKMRH LLHVLKVDLG CTSEENSVKQ NDVDMLNVFD FEKAGNSEPN ELKNESEVTI QQERQQYQKA LDMLLSAPKD ENEIFPSPTE FFMPIYKSKH SEGVIIQQVN DETNLETSTL DENHPSISDS LTDRETSVNV IEGDSDPEKV EISNGLCGLN TSPSQSVQFS SVKGDNNHDM ELSTLKIMEM SIEDCPLDV

Frequently asked questions

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

Which diseases are associated with SPATA7?

The strongest Open Targets associations for SPATA7 are Leber congenital amaurosis, retinitis pigmentosa, Retinal dystrophy, retinitis pigmentosa 94, variable age at onset and severe early-childhood-onset retinal dystrophy.

How long is the SPATA7 protein?

The Homo sapiens SPATA7 protein (UniProt Q9P0W8) is 599 amino acids long.

Browse: Targets: S · 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

UniProtQ9P0W8
GeneSPATA7
OrganismHomo sapiens
Length599
Binders0
Diseases49
View on UniProt