Rhox homeobox family member 1 (RHOXF1)

Homo sapiens — UniProt Q8NHV9

Gene: RHOXF1Homo sapiensSwissProt reviewed

About Rhox homeobox family member 1

Rhox homeobox family member 1 (RHOXF1) is a protein from Homo sapiens identified by UniProt accession Q8NHV9, 184 residues long. MolForge cross-references it against 0 known binders and 88 disease associations.

Target properties

Protein nameRhox homeobox family member 1
UniProt accessionQ8NHV9
GeneRHOXF1
OrganismHomo sapiens
Length184 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (88)

Diseases linked to this target (Open Targets).

  • azoospermia · score 0.10
  • male infertility with teratozoospermia due to single gene mutation · score 0.08
  • partial chromosome Y deletion · score 0.08
  • spermatogenic failure 8 · score 0.07
  • spermatogenic failure 1 · score 0.07
  • spermatogenic failure 25 · score 0.07
  • spermatogenic failure 48 · score 0.07
  • spermatogenic failure 51 · score 0.07
  • spermatogenic failure, X-linked, 3 · score 0.07
  • spermatogenic failure 40 · score 0.07

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8NHV9-F1alphafoldPREDICTED64.27—

Amino-acid sequence (184 residues)

MARSLVHDTV FYCLSVYQVK ISPTPQLGAA SSAEGHVGQG APGLMGNMNP EGGVNHENGM NRDGGMIPEG GGGNQEPRQQ PQPPPEEPAQ AAMEGPQPEN MQPRTRRTKF TLLQVEELES VFRHTQYPDV PTRRELAENL GVTEDKVRVW FKNKRARCRR HQRELMLANE LRADPDDCVY IVVD

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Quick facts

UniProtQ8NHV9
GeneRHOXF1
OrganismHomo sapiens
Length184
Binders0
Diseases88
View on UniProt