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tRNA methyltransferase 10 homolog A (TRMT10A)

Homo sapiens — UniProt Q8TBZ6

Gene: TRMT10AHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

tRNA methyltransferase 10 homolog A (TRMT10A) is a protein from Homo sapiens identified by UniProt accession Q8TBZ6, 339 residues long. MolForge cross-references it against 0 known binders and 64 disease associations.

  • UniProt accession: Q8TBZ6; gene symbol TRMT10A.
  • Organism: Homo sapiens.
  • Length: 339 amino acids.
  • Top disease associations (Open Targets): primary microcephaly-mild intellectual disability-young-onset diabetes syndrome, genetic disorder and autosomal recessive non-syndromic intellectual disability.
  • 3D structure: AlphaFold model available.

Target properties

Protein nametRNA methyltransferase 10 homolog A
UniProt accessionQ8TBZ6
GeneTRMT10A
OrganismHomo sapiens
Length339 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 (64)

Diseases linked to this target (Open Targets).

  • primary microcephaly-mild intellectual disability-young-onset diabetes syndrome · score 0.71
  • genetic disorder · score 0.47
  • autosomal recessive non-syndromic intellectual disability · score 0.46
  • Primary microcephaly · score 0.37
  • Abnormality of the nervous system · score 0.27
  • serum alanine aminotransferase measurement · score 0.17
  • body height · score 0.13
  • platelet component distribution width · score 0.13
  • aspartate aminotransferase measurement · score 0.13
  • high density lipoprotein cholesterol measurement · score 0.12

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8TBZ6-F1alphafoldPREDICTED76.07—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q8TBZ6.

Amino-acid sequence (339 residues)

MSSEMLPAFI ETSNVDKKQG INEDQEESQK PRLGEGCEPI SKRQMKKLIK QKQWEEQREL RKQKRKEKRK RKKLERQCQM EPNSDGHDRK RVRRDVVHST LRLIIDCSFD HLMVLKDIKK LHKQIQRCYA ENRRALHPVQ FYLTSHGGQL KKNMDENDKG WVNWKDIHIK PEHYSELIKK EDLIYLTSDS PNILKELDES KAYVIGGLVD HNHHKGLTYK QASDYGINHA QLPLGNFVKM NSRKVLAVNH VFEIILEYLE TRDWQEAFFT ILPQRKGAVP TDKACESASH DNQSVRMEEG GSDSDSSEEE YSRNELDSPH EEKQDKENHT ESTVNSLPH

Frequently asked questions

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

Which diseases are associated with TRMT10A?

The strongest Open Targets associations for TRMT10A are primary microcephaly-mild intellectual disability-young-onset diabetes syndrome, genetic disorder, autosomal recessive non-syndromic intellectual disability, Primary microcephaly and Abnormality of the nervous system.

How long is the TRMT10A protein?

The Homo sapiens TRMT10A protein (UniProt Q8TBZ6) is 339 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

UniProtQ8TBZ6
GeneTRMT10A
OrganismHomo sapiens
Length339
Binders0
Diseases64
View on UniProt