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PR domain zinc finger protein 13 (PRDM13)

Homo sapiens — UniProt Q9H4Q3

Gene: PRDM13Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

PR domain zinc finger protein 13 (PRDM13) is a protein from Homo sapiens identified by UniProt accession Q9H4Q3, 707 residues long. MolForge cross-references it against 0 known binders and 144 disease associations.

  • UniProt accession: Q9H4Q3; gene symbol PRDM13.
  • Organism: Homo sapiens.
  • Length: 707 amino acids.
  • Top disease associations (Open Targets): cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, pontocerebellar hypoplasia, IIA 17 and North Carolina macular dystrophy.
  • 3D structure: AlphaFold model available.

Target properties

Protein namePR domain zinc finger protein 13
UniProt accessionQ9H4Q3
GenePRDM13
OrganismHomo sapiens
Length707 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 (144)

Diseases linked to this target (Open Targets).

  • cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism · score 0.64
  • pontocerebellar hypoplasia, IIA 17 · score 0.62
  • North Carolina macular dystrophy · score 0.48
  • congenital hypogonadotropic hypogonadism · score 0.42
  • genetic disorder · score 0.41
  • testosterone measurement · score 0.38
  • age at menarche · score 0.37
  • neurodegenerative disease · score 0.37
  • enuresis · score 0.36
  • body height · score 0.34

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H4Q3-F1alphafoldPREDICTED52.19—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H4Q3.

Amino-acid sequence (707 residues)

MHGAARAPAT SVSADCCIPA GLRLGPVPGT FKLGKYLSDR REPGPKKKVR MVRGELVDES GGSPLEWIGL IRAARNSQEQ TLEAIADLPG GQIFYRALRD VQPGEELTVW YSNSLAQWFD IPTTATPTHD EKGEERYICW YCWRTFRYPN SLKAHLRFHC VFSGGGGGAF LHHEHAARQG AVPAADGLGL SPKPPAPDFA APSQAGTLRP HPLGPPPVQA CGAREGIKRE ASSAPSATSP TPGKWGQPKK GKEQLDRALD MSGAARGQGH FLGIVGGSSA GVGSLAFYPG VRSAFKPAGL ARAAAAAHGD PYREESSSKQ GAGLALGRLL GGGRACGRPG SGENSAAGGA GHHHHHHAHH HHHPKCLLAG DPPPPPPPGL PCSGALRGFP LLSVPPEEAS AFKHVERAPP AAAALPGARY AQLPPAPGLP LERCALPPLD PGGLKAYPGG ECSHLPAVMP AFTVYNGELL YGSPATTAYY PLKLHFGGLL KYPESISYFS GPAAAALSPA ELGSLASIDR EIAMHNQQLS EMAAGKGRGR LDSGTLPPAV AAAGGTGGGG SGGSGAGKPK TGHLCLYCGK LYSRKYGLKI HMRTHTGYKP LKCKVCLRPF GDPSNLNKHI RLHAEGNTPY RCEFCGKVLV RRRDLERHVK SRHPGQSLLA KAGDGPGAEP GYPPEPGDPK SDDSDVDVCF TDDQSDPEVG GGGERDL

Frequently asked questions

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

Which diseases are associated with PRDM13?

The strongest Open Targets associations for PRDM13 are cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, pontocerebellar hypoplasia, IIA 17, North Carolina macular dystrophy, congenital hypogonadotropic hypogonadism and genetic disorder.

How long is the PRDM13 protein?

The Homo sapiens PRDM13 protein (UniProt Q9H4Q3) is 707 amino acids long.

Browse: Targets: P · 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

UniProtQ9H4Q3
GenePRDM13
OrganismHomo sapiens
Length707
Binders0
Diseases144
View on UniProt