Skip to content

Taperin (TPRN)

Homo sapiens — UniProt Q4KMQ1

Gene: TPRNHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Taperin (TPRN) is a protein from Homo sapiens identified by UniProt accession Q4KMQ1, 711 residues long. MolForge cross-references it against 0 known binders and 22 disease associations.

  • UniProt accession: Q4KMQ1; gene symbol TPRN.
  • Organism: Homo sapiens.
  • Length: 711 amino acids.
  • Top disease associations (Open Targets): deafness, hearing loss, autosomal recessive and Rare genetic deafness.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTaperin
UniProt accessionQ4KMQ1
GeneTPRN
OrganismHomo sapiens
Length711 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 (22)

Diseases linked to this target (Open Targets).

  • deafness · score 0.64
  • hearing loss, autosomal recessive · score 0.63
  • Rare genetic deafness · score 0.46
  • nonsyndromic genetic hearing loss · score 0.37
  • hearing loss · score 0.37
  • ear malformation · score 0.27
  • Abnormality of the ear · score 0.27
  • genetic disorder · score 0.19
  • Hearing impairment · score 0.12
  • balding measurement · score 0.11

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q4KMQ1-F1alphafoldPREDICTED54.45—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q4KMQ1.

Amino-acid sequence (711 residues)

MAALGRPGSG PRAAVPAWKR EILERKRAKL AALGGGAGPG AAEPEQRVLA ESLGPLRENP FMLLEAERRR GGGAAGARLL ERYRRVPGVR ALRADSVLII ETVPGFPPAP PAPGAAQIRA AEVLVYGAPP GRVSRLLERF DPPAAPRRRG SPERARPPPP PPPPAPPRPP PAAPSPPAAP GPRGGGASPG ARRSDFLQKT GSNSFTVHPR GLHRGAGARL LSNGHSAPEP RAGPANRLAG SPPGSGQWKP KVESGDPSLH PPPSPGTPSA TPASPPASAT PSQRQCVSAA TSTNDSFEIR PAPKPVMETI PLGDLQARAL ASLRANSRNS FMVIPKSKAS GAPPPEGRQS VELPKGDLGP ASPSQELGSQ PVPGGDGAPA LGKSPLEVEA QWAVEEGACP RTATALADRA IRWQRPSSPP PFLPAASEEA EPAEGLRVPG LAKNSREYVR PGLPVTFIDE VDSEEAPQAA KLPYLPHPAR PLHPARPGCV AELQPRGSNT FTVVPKRKPG TLQDQHFSQA NREPRPREAE EEEASCLLGP TLKKRYPTVH EIEVIGGYLA LQKSCLTKAG SSRKKMKISF NDKSLQTTFE YPSESSLEQE EEVDQQEEEE EEEEEEEEEE EGSGSEEKPF ALFLPRATFV SSVRPESSRL PEGSSGLSSY TPKHSVAFSK WQEQALEQAP REAEPPPVEA MLTPASQNDL SDFRSEPALY F

Frequently asked questions

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

Which diseases are associated with TPRN?

The strongest Open Targets associations for TPRN are deafness, hearing loss, autosomal recessive, Rare genetic deafness, nonsyndromic genetic hearing loss and hearing loss.

How long is the TPRN protein?

The Homo sapiens TPRN protein (UniProt Q4KMQ1) is 711 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.

Explore Taperin 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

UniProtQ4KMQ1
GeneTPRN
OrganismHomo sapiens
Length711
Binders0
Diseases22
View on UniProt