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Tectonic-2 (TCTN2)

Homo sapiens — UniProt Q96GX1

Gene: TCTN2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Tectonic-2 (TCTN2) is a protein from Homo sapiens identified by UniProt accession Q96GX1, 697 residues long. MolForge cross-references it against 0 known binders and 68 disease associations.

  • UniProt accession: Q96GX1; gene symbol TCTN2.
  • Organism: Homo sapiens.
  • Length: 697 amino acids.
  • Top disease associations (Open Targets): Joubert syndrome, Meckel syndrome and Joubert syndrome and related disorders.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTectonic-2
UniProt accessionQ96GX1
GeneTCTN2
OrganismHomo sapiens
Length697 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 (68)

Diseases linked to this target (Open Targets).

  • Joubert syndrome · score 0.76
  • Meckel syndrome · score 0.73
  • Joubert syndrome and related disorders · score 0.68
  • low density lipoprotein cholesterol measurement · score 0.25
  • genetic disorder · score 0.19
  • body fat percentage · score 0.15
  • Microcephaly · score 0.11
  • cancer · score 0.07
  • FEV/FVC ratio · score 0.07
  • leukocyte count · score 0.06

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96GX1-F1alphafoldPREDICTED74.47—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q96GX1.

Amino-acid sequence (697 residues)

MGFQPPAALL LRLFLLQGIL RLLWGDLAFI PPFIRMSGPA VSASLVGDTE GVTVSLAVLQ DEAGILPIPT CGVLNNETED WSVTVIPGAK VLEVTVRWKR GLDWCSSNET DSFSESPCIL QTLLVSASHN SSCSAHLLIQ VEIYANSSLT HNASENVTVI PNQVYQPLGP CPCNLTAGAC DVRCCCDQEC SSNLTTLFRR SCFTGVFGGD VNPPFDQLCS AGTTTRGVPD WFPFLCVQSP LANTPFLGYF YHGAVSPKQD SSFEVYVDTD AKDFADFGYK QGDPIMTVKK AYFTIPQVSL AGQCMQNAPV AFLHNFDVKC VTNLELYQER DGIINAKIKN VALGGIVTPK VIYEEATDLD KFITNTETPL NNGSTPRIVN VEEHYIFKWN NNTISEINVK IFRAEINAHQ KGIMTQRFVV KFLSYNSGNE EELSGNPGYQ LGKPVRALNI NRMNNVTTLH LWQSAGRGLC TSATFKPILF GENVLSGCLL EVGINENCTQ LRENAVERLD SLIQATHVAM RGNSDYADLS DGWLEIIRVD APDPGADPLA SSVNGMCLDI PAHLSIRILI SDAGAVEGIT QQEILGVETR FSSVNWQYQC GLTCEHKADL LPISASVQFI KIPAQLPHPL TRFQINYTEY DCNRNEVCWP QLLYPWTQYY QGELHSQCVA KGLLLLLFLT LALFLSNPWT RICKAYS

Frequently asked questions

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

Which diseases are associated with TCTN2?

The strongest Open Targets associations for TCTN2 are Joubert syndrome, Meckel syndrome, Joubert syndrome and related disorders, low density lipoprotein cholesterol measurement and genetic disorder.

How long is the TCTN2 protein?

The Homo sapiens TCTN2 protein (UniProt Q96GX1) is 697 amino acids long.

Browse: Targets: T · 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

UniProtQ96GX1
GeneTCTN2
OrganismHomo sapiens
Length697
Binders0
Diseases68
View on UniProt