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Golgi pH regulator A (GPR89A)

Homo sapiens — UniProt B7ZAQ6

Gene: GPR89AHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Golgi pH regulator A (GPR89A) is a protein from Homo sapiens identified by UniProt accession B7ZAQ6, 455 residues long. MolForge cross-references it against 0 known binders and 17 disease associations.

  • UniProt accession: B7ZAQ6; gene symbol GPR89A.
  • Organism: Homo sapiens.
  • Length: 455 amino acids.
  • Top disease associations (Open Targets): Okt4 epitope deficiency, combined immunodeficiency with skin granulomas and 22q11.2 deletion syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameGolgi pH regulator A
UniProt accessionB7ZAQ6
GeneGPR89A
OrganismHomo sapiens
Length455 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 (17)

Diseases linked to this target (Open Targets).

  • Okt4 epitope deficiency · score 0.05
  • combined immunodeficiency with skin granulomas · score 0.03
  • 22q11.2 deletion syndrome · score 0.03
  • X-Linked Combined Immunodeficiency Diseases · score 0.03
  • Alymphoid cystic thymic dysgenesis · score 0.03
  • immunodeficiency 19 · score 0.03
  • immunodeficiency 18 · score 0.03
  • uric acid measurement · score 0.03
  • urate measurement · score 0.02
  • Thrombocytopenia · score 0.00

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-B7ZAQ6-F1alphafoldPREDICTED82.33—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for B7ZAQ6.

Amino-acid sequence (455 residues)

MSFLIDSSIM ITSQILFFGF GWLFFMRQLF KDYEIRQYVV QVIFSVTFAF SCTMFELIIF EILGVLNSSS RYFHWKMNLC VILLILVFMV PFYIGYFIVS NIRLLHKQRL LFSCLLWLTF MYFFWKLGDP FPILSPKHGI LSIEQLISRV GVIGVTLMAL LSGFGAVNCP YTYMSYFLRN VTDTDILALE RRLLQTMDMI ISKKKRMAMA RRTMFQKGEV HNKPSGFWGM IKSVTTSASG SENLTLIQQE VDALEELSRQ LFLETADLYA TKERIEYSKT FKGKYFNFLG YFFSIYCVWK IFMATINIVF DRVGKTDPVT RGIEITVNYL GIQFDVKFWS QHISFILVGI IIVTSIRGLL ITLTKFFYAI SSSKSSNVIV LLLAQIMGMY FVSSVLLIRM SMPLEYRTII TEVLGELQFN FYHRWFDVIF LVSALSSILF LYLAHKQAPE KQMAP

Frequently asked questions

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

Which diseases are associated with GPR89A?

The strongest Open Targets associations for GPR89A are Okt4 epitope deficiency, combined immunodeficiency with skin granulomas, 22q11.2 deletion syndrome, X-Linked Combined Immunodeficiency Diseases and Alymphoid cystic thymic dysgenesis.

How long is the GPR89A protein?

The Homo sapiens GPR89A protein (UniProt B7ZAQ6) is 455 amino acids long.

Browse: Targets: G · 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

UniProtB7ZAQ6
GeneGPR89A
OrganismHomo sapiens
Length455
Binders0
Diseases17
View on UniProt