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Cytospin-A (SPECC1L)

Homo sapiens — UniProt Q69YQ0

Gene: SPECC1LHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Cytospin-A (SPECC1L) is a protein from Homo sapiens identified by UniProt accession Q69YQ0, 1117 residues long. MolForge cross-references it against 0 known binders and 121 disease associations.

  • UniProt accession: Q69YQ0; gene symbol SPECC1L.
  • Organism: Homo sapiens.
  • Length: 1117 amino acids.
  • Top disease associations (Open Targets): Teebi hypertelorism syndrome 1, Hypertelorism, Teebi type and Tessier number 4 facial cleft.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameCytospin-A
UniProt accessionQ69YQ0
GeneSPECC1L
OrganismHomo sapiens
Length1117 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 (121)

Diseases linked to this target (Open Targets).

  • Teebi hypertelorism syndrome 1 · score 0.66
  • Hypertelorism, Teebi type · score 0.64
  • Tessier number 4 facial cleft · score 0.62
  • Teebi hypertelorism syndrome · score 0.52
  • neurodegenerative disease · score 0.49
  • serum gamma-glutamyl transferase measurement · score 0.46
  • Intellectual disability · score 0.44
  • lateral facial cleft · score 0.37
  • oculomaxillofacial dysostosis · score 0.36
  • Opitz G/BBB syndrome · score 0.36

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q69YQ0-F1alphafoldPREDICTED65.57—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q69YQ0.

Amino-acid sequence (1117 residues)

MKKASRSVGS VPKVSAISKT QTAEKIKPEN SSSASTGGKL VKPGTAASLS KTKSSDDLLA GMAGGVTVTN GVKGKKSTCP SAAPSASAPA MTTVENKSKI STGTASSTKR STSTGNKESS STRERLRERT RLNQSKKLPS AGQGANDMAL AKRSRSRTAT ECDVRMSKSK SDNQISDRAA LEAKVKDLLT LAKTKDVEIL HLRNELRDMR AQLGINEDHS EGDEKSEKET IMAHQPTDVE STLLQLQEQN TAIREELNQL KNENRMLKDR LNALGFSLEQ RLDNSEKLFG YQSLSPEITP GNQSDGGGTL TSSVEGSAPG SVEDLLSQDE NTLMDHQHSN SMDNLDSECS EVYQPLTSSD DALDAPSSSE SEGIPSIERS RKGSSGNASE VSVACLTERI HQMEENQHST SEELQATLQE LADLQQITQE LNSENERLGE EKVILMESLC QQSDKLEHFS RQIEYFRSLL DEHHISYVID EDVKSGRYME LEQRYMDLAE NARFEREQLL GVQQHLSNTL KMAEQDNKEA QEMIGALKER SHHMERIIES EQKGKAALAA TLEEYKATVA SDQIEMNRLK AQLENEKQKV AELYSIHNSG DKSDIQDLLE SVRLDKEKAE TLASSLQEDL AHTRNDANRL QDAIAKVEDE YRAFQEEAKK QIEDLNMTLE KLRSDLDEKE TERSDMKETI FELEDEVEQH RAVKLHDNLI ISDLENTVKK LQDQKHDMER EIKTLHRRLR EESAEWRQFQ ADLQTAVVIA NDIKSEAQEE IGDLKRRLHE AQEKNEKLTK ELEEIKSRKQ EEERGRVYNY MNAVERDLAA LRQGMGLSRR SSTSSEPTPT VKTLIKSFDS ASQVPNPAAA AIPRTPLSPS PMKTPPAAAV SPMQRHSISG PISTSKPLTA LSDKRPNYGE IPVQEHLLRT SSASRPASLP RVPAMESAKT LSVSRRSSEE VKRDISAQEG ASPASLMAMG TTSPQLSLSS SPTASVTPTT RSRIREERKD PLSALAREYG GSKRNALLKW CQKKTEGYQN IDITNFSSSW NDGLAFCALL HTYLPAHIPY QELNSQDKRR NFMLAFQAAE SVGIKSTLDI NEMVRTERPD WQNVMLYVTA IYKYFET

Frequently asked questions

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

Which diseases are associated with SPECC1L?

The strongest Open Targets associations for SPECC1L are Teebi hypertelorism syndrome 1, Hypertelorism, Teebi type, Tessier number 4 facial cleft, Teebi hypertelorism syndrome and neurodegenerative disease.

How long is the SPECC1L protein?

The Homo sapiens SPECC1L protein (UniProt Q69YQ0) is 1117 amino acids long.

Browse: Targets: S · 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

UniProtQ69YQ0
GeneSPECC1L
OrganismHomo sapiens
Length1117
Binders0
Diseases121
View on UniProt