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TERF1-interacting nuclear factor 2 (TINF2)

Homo sapiens — UniProt Q9BSI4

Gene: TINF2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

TERF1-interacting nuclear factor 2 (TINF2) is a protein from Homo sapiens identified by UniProt accession Q9BSI4, 451 residues long. MolForge cross-references it against 0 known binders and 104 disease associations.

  • UniProt accession: Q9BSI4; gene symbol TINF2.
  • Organism: Homo sapiens.
  • Length: 451 amino acids.
  • Top disease associations (Open Targets): dyskeratosis congenita, autosomal dominant 3, Revesz syndrome and dyskeratosis congenita.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTERF1-interacting nuclear factor 2
UniProt accessionQ9BSI4
GeneTINF2
OrganismHomo sapiens
Length451 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 (104)

Diseases linked to this target (Open Targets).

  • dyskeratosis congenita, autosomal dominant 3 · score 0.79
  • Revesz syndrome · score 0.78
  • dyskeratosis congenita · score 0.72
  • neurodegenerative disease · score 0.53
  • Hoyeraal-Hreidarsson syndrome · score 0.37
  • head and neck squamous cell carcinoma · score 0.26
  • endometrial cancer · score 0.24
  • glioblastoma multiforme · score 0.23
  • gastric adenocarcinoma · score 0.21
  • lung adenocarcinoma · score 0.21

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9BSI4-F1alphafoldPREDICTED60.56—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9BSI4.

Amino-acid sequence (451 residues)

MATPLVAGPA ALRFAAAASW QVVRGRCVEH FPRVLEFLRS LRAVAPGLVR YRHHERLCMG LKAKVVVELI LQGRPWAQVL KALNHHFPES GPIVRDPKAT KQDLRKILEA QETFYQQVKQ LSEAPVDLAS KLQELEQEYG EPFLAAMEKL LFEYLCQLEK ALPTPQAQQL QDVLSWMQPG VSITSSLAWR QYGVDMGWLL PECSVTDSVN LAEPMEQNPP QQQRLALHNP LPKAKPGTHL PQGPSSRTHP EPLAGRHFNL APLGRRRVQS QWASTRGGHK ERPTVMLFPF RNLGSPTQVI SKPESKEEHA IYTADLAMGT RAASTGKSKS PCQTLGGRAL KENPVDLPAT EQKENCLDCY MDPLRLSLLP PRARKPVCPP SLCSSVITIG DLVLDSDEEE NGQGEGKESL ENYQKTKFDT LIPTLCEYLP PSGHGAIPVS SCDCRDSSRP L

Frequently asked questions

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

Which diseases are associated with TINF2?

The strongest Open Targets associations for TINF2 are dyskeratosis congenita, autosomal dominant 3, Revesz syndrome, dyskeratosis congenita, neurodegenerative disease and Hoyeraal-Hreidarsson syndrome.

How long is the TINF2 protein?

The Homo sapiens TINF2 protein (UniProt Q9BSI4) is 451 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

UniProtQ9BSI4
GeneTINF2
OrganismHomo sapiens
Length451
Binders0
Diseases104
View on UniProt