Skip to content

Chaperonin-containing T-complex member BBS12 (BBS12)

Homo sapiens — UniProt Q6ZW61

Gene: BBS12Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Chaperonin-containing T-complex member BBS12 (BBS12) is a protein from Homo sapiens identified by UniProt accession Q6ZW61, 710 residues long. MolForge cross-references it against 0 known binders and 113 disease associations.

  • UniProt accession: Q6ZW61; gene symbol BBS12.
  • Organism: Homo sapiens.
  • Length: 710 amino acids.
  • Top disease associations (Open Targets): Bardet-Biedl syndrome 12, Bardet-Biedl syndrome and Bardet-Biedl syndrome 1.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameChaperonin-containing T-complex member BBS12
UniProt accessionQ6ZW61
GeneBBS12
OrganismHomo sapiens
Length710 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 (113)

Diseases linked to this target (Open Targets).

  • Bardet-Biedl syndrome 12 · score 0.83
  • Bardet-Biedl syndrome · score 0.67
  • Bardet-Biedl syndrome 1 · score 0.56
  • Retinal dystrophy · score 0.51
  • Polydactyly · score 0.46
  • polydactyly · score 0.46
  • Obesity · score 0.37
  • ciliopathy · score 0.37
  • obesity · score 0.37
  • lymphocyte count · score 0.36

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q6ZW61-F1alphafoldPREDICTED74.01—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q6ZW61.

Amino-acid sequence (710 residues)

MVMACRVVNK RRHMGLQQLS SFAETGRTFL GPLKSSKFII DEECHESVLI SSTVRLLESL DLTSAVGQLL NEAVQAQNNT YRTGISTLLF LVGAWSSAVE ECLHLGVPIS IIVSVMSEGL NFCSEEVVSL HVPVHNIFDC MDSTKTFSQL ETFSVSLCPF LQVPSDTDLI EELHGLKDVA SQTLTISNLS GRPLKSYELF KPQTKVEADN NTSRTLKNSL LADTCCRQSI LIHSRHFNRT DNTEGVSKPD GFQEHVTATH KTYRCNDLVE LAVGLSHGDH SSMKLVEEAV QLQYQNACVQ QGNCTKPFMF DISRIFTCCL PGLPETSSCV CPGYITVVSV SNNPVIKELQ NQPVRIVLIE GDLTENYRHL GFNKSANIKT VLDSMRLQED SSEELWANHV LQVLIQFKVN LVLVQGNVSE RLIEKCINSK RLVIGSVNGS VMQAFAEAAG AVQVAYITQV NEDCVGDGVC VTFWRSSPLD VVDRNNRIAI LLKTEGINLV TAVLTNPVTA QMQIKEDRFW TCAYRLYYAL KEEKVFLGGG AVEFLCLSCL HILAEQSLKK ENHACSGWLH NTSSWLASSL AIYRPTVLKF LANGWQKYLS TLLYNTANYS SEFEASTYIQ HHLQNATDSG SPSSYILNEY SKLNSRIFNS DISNKLEQIP RVYDVVTPKI EAWRRALDLV LLVLQTDSEI ITGHGHTQIN SQELTGFLFL

Frequently asked questions

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

Which diseases are associated with BBS12?

The strongest Open Targets associations for BBS12 are Bardet-Biedl syndrome 12, Bardet-Biedl syndrome, Bardet-Biedl syndrome 1, Retinal dystrophy and Polydactyly.

How long is the BBS12 protein?

The Homo sapiens BBS12 protein (UniProt Q6ZW61) is 710 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.

Explore Chaperonin-containing T-complex member BBS12 with MolForge

Find binders, run structure-based screening, and map this target across diseases and approved drugs with our AI-powered platform.

Browse all targets

Quick facts

UniProtQ6ZW61
GeneBBS12
OrganismHomo sapiens
Length710
Binders0
Diseases113
View on UniProt