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N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 (B3GNT4)

Homo sapiens — UniProt Q9C0J1

Gene: B3GNT4Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 (B3GNT4) is a protein from Homo sapiens identified by UniProt accession Q9C0J1, 378 residues long. MolForge cross-references it against 0 known binders and 15 disease associations.

  • UniProt accession: Q9C0J1; gene symbol B3GNT4.
  • Organism: Homo sapiens.
  • Length: 378 amino acids.
  • Top disease associations (Open Targets): autosomal dominant nonsyndromic hearing loss, Hearing impairment and deafness.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameN-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4
UniProt accessionQ9C0J1
GeneB3GNT4
OrganismHomo sapiens
Length378 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 (15)

Diseases linked to this target (Open Targets).

  • autosomal dominant nonsyndromic hearing loss · score 0.12
  • Hearing impairment · score 0.12
  • deafness · score 0.12
  • lean body mass · score 0.11
  • body height · score 0.09
  • fat body mass · score 0.08
  • C-reactive protein measurement · score 0.08
  • self reported educational attainment · score 0.04
  • body mass index · score 0.03
  • osteosarcoma · score 0.02

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9C0J1-F1alphafoldPREDICTED86.89—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9C0J1.

Amino-acid sequence (378 residues)

MLPPQPSAAH QGRGGRSGLL PKGPAMLCRL CWLVSYSLAV LLLGCLLFLR KAAKPAGDPT AHQPFWAPPT PRHSRCPPNH TVSSASLSLP SRHRLFLTYR HCRNFSILLE PSGCSKDTFL LLAIKSQPGH VERRAAIRST WGRVGGWARG RQLKLVFLLG VAGSAPPAQL LAYESREFDD ILQWDFTEDF FNLTLKELHL QRWVVAACPQ AHFMLKGDDD VFVHVPNVLE FLDGWDPAQD LLVGDVIRQA LPNRNTKVKY FIPPSMYRAT HYPPYAGGGG YVMSRATVRR LQAIMEDAEL FPIDDVFVGM CLRRLGLSPM HHAGFKTFGI RRPLDPLDPC LYRGLLLVHR LSPLEMWTMW ALVTDEGLKC AAGPIPQR

Frequently asked questions

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

Which diseases are associated with B3GNT4?

The strongest Open Targets associations for B3GNT4 are autosomal dominant nonsyndromic hearing loss, Hearing impairment, deafness, lean body mass and body height.

How long is the B3GNT4 protein?

The Homo sapiens B3GNT4 protein (UniProt Q9C0J1) is 378 amino acids long.

Browse: Targets: B · 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

UniProtQ9C0J1
GeneB3GNT4
OrganismHomo sapiens
Length378
Binders0
Diseases15
View on UniProt