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Primary cilium assembly protein FAM149B1 (FAM149B1)

Homo sapiens — UniProt Q96BN6

Gene: FAM149B1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Primary cilium assembly protein FAM149B1 (FAM149B1) is a protein from Homo sapiens identified by UniProt accession Q96BN6, 582 residues long. MolForge cross-references it against 0 known binders and 82 disease associations.

  • UniProt accession: Q96BN6; gene symbol FAM149B1.
  • Organism: Homo sapiens.
  • Length: 582 amino acids.
  • Top disease associations (Open Targets): Joubert syndrome 36, neurodegenerative disease and orofaciodigital syndrome type 6.
  • 3D structure: AlphaFold model available.

Target properties

Protein namePrimary cilium assembly protein FAM149B1
UniProt accessionQ96BN6
GeneFAM149B1
OrganismHomo sapiens
Length582 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 (82)

Diseases linked to this target (Open Targets).

  • Joubert syndrome 36 · score 0.60
  • neurodegenerative disease · score 0.44
  • orofaciodigital syndrome type 6 · score 0.37
  • syndromic intellectual disability · score 0.37
  • Joubert syndrome · score 0.33
  • orofaciodigital syndrome · score 0.26
  • serum alanine aminotransferase measurement · score 0.14
  • azoospermia · score 0.09
  • Male infertility with spermatogenesis disorder due to single gene mutation · score 0.07
  • Female infertility due to fertilization defect · score 0.07

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96BN6-F1alphafoldPREDICTED51.98—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q96BN6.

Amino-acid sequence (582 residues)

MISRYTRKAV PQSLELKGIT KHALNHHPPP EKLEEISPTS DSHEKDTSSQ SKSDITRESS FTSADTGNSL SAFPSYTGAG ISTEGSSDFS WGYGELDQNA TEKVQTMFTA IDELLYEQKL SVHTKSLQEE CQQWTASFPH LRILGRQIIT PSEGYRLYPR SPSAVSASYE TTLSQERDST IFGIRGKKLH FSSSYAHKAS SIAKSSSFCS MERDEEDSII VSEGIIEEYL AFDHIDIEEG FHGKKSEAAT EKQKLGYPPI APFYCMKEDV LAYVFDSVWC KVVSCMEQLT RSHWEGFASD DESNVAVTRP DSESSCVLSE LHPLVLPRVP QSKVLYITSN PMSLCQASRH QPNVNDLLVH GMPLQPRNLS LMDKLLDLDD KLLMRPGSST ILSTRNWPNR AVEFSTSSLS YTVQSTRRRN PPPRTLHPIS TSHSCAETPR SVEEILRGAR VPVAPDSLSS PSPTPLSRNN LLPPIGTAEV EHVSTVGPQR QMKPHGDSSR AQSAVVDEPN YQQPQERLLL PDFFPRPNTT QSFLLDTQYR RSCAVEYPHQ ARPGRGSAGP QLHGSTKSQS GGRPVSRTRQ GP

Frequently asked questions

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

Which diseases are associated with FAM149B1?

The strongest Open Targets associations for FAM149B1 are Joubert syndrome 36, neurodegenerative disease, orofaciodigital syndrome type 6, syndromic intellectual disability and Joubert syndrome.

How long is the FAM149B1 protein?

The Homo sapiens FAM149B1 protein (UniProt Q96BN6) is 582 amino acids long.

Browse: Targets: F · 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

UniProtQ96BN6
GeneFAM149B1
OrganismHomo sapiens
Length582
Binders0
Diseases82
View on UniProt