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Dystrobrevin alpha (DTNA)

Homo sapiens — UniProt Q9Y4J8

Gene: DTNAHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Dystrobrevin alpha (DTNA) is a protein from Homo sapiens identified by UniProt accession Q9Y4J8, 743 residues long. MolForge cross-references it against 0 known binders and 141 disease associations.

  • UniProt accession: Q9Y4J8; gene symbol DTNA.
  • Organism: Homo sapiens.
  • Length: 743 amino acids.
  • Top disease associations (Open Targets): dilated cardiomyopathy, left ventricular noncompaction and Meniere disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameDystrobrevin alpha
UniProt accessionQ9Y4J8
GeneDTNA
OrganismHomo sapiens
Length743 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 (141)

Diseases linked to this target (Open Targets).

  • dilated cardiomyopathy · score 0.33
  • left ventricular noncompaction · score 0.32
  • Meniere disease · score 0.31
  • mathematical ability · score 0.30
  • cardiac arrhythmia · score 0.27
  • Varicose veins · score 0.23
  • PR interval · score 0.23
  • chronotype measurement · score 0.23
  • metabolite measurement · score 0.20
  • Muscular dystrophy · score 0.19

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y4J8-F1alphafoldPREDICTED69.03—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y4J8.

Amino-acid sequence (743 residues)

MIEDSGKRGN TMAERRQLFA EMRAQDLDRI RLSTYRTACK LRFVQKKCNL HLVDIWNVIE ALRENALNNL DPNTELNVSR LEAVLSTIFY QLNKRMPTTH QIHVEQSISL LLNFLLAAFD PEGHGKISVF AVKMALATLC GGKIMDKLRY IFSMISDSSG VMVYGRYDQF LREVLKLPTA VFEGPSFGYT EQSARSCFSQ QKKVTLNGFL DTLMSDPPPQ CLVWLPLLHR LANVENVFHP VECSYCHSES MMGFRYRCQQ CHNYQLCQDC FWRGHAGGSH SNQHQMKEYT SWKSPAKKLT NALSKSLSCA SSREPLHPMF PDQPEKPLNL AHIVDTWPPR PVTSMNDTLF SHSVPSSGSP FITRSSPPKD SEVEQNKLLA RAAPAFLKGK GIQYSLNVAD RLADEHVLIG LYVNMLRNNP SCMLESSNRL DEEHRLIARY AARLAAESSS SQPPQQRSAP DISFTIDANK QQRQLIAELE NKNREILQEI QRLRLEHEQA SQPTPEKAQQ NPTLLAELRL LRQRKDELEQ RMSALQESRR ELMVQLEGLM KLLKTQGAGS PRSSPSHTIS RPIPMPIRSA SACSTPTHTP QDSLTGVGGD VQEAFAQSSR RNLRNDLLVA ADSITNTMSS LVKELNSEVG SETESNVDSE FARTQFEDLV PSPTSEKAFL AQIHARKPGY IHSGATTSTM RGDMVTEDAD PYVQPEDENY ENDSVRQLEN ELQMEEYLKQ KLQDEAYQVS LQG

Frequently asked questions

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

Which diseases are associated with DTNA?

The strongest Open Targets associations for DTNA are dilated cardiomyopathy, left ventricular noncompaction, Meniere disease, mathematical ability and cardiac arrhythmia.

How long is the DTNA protein?

The Homo sapiens DTNA protein (UniProt Q9Y4J8) is 743 amino acids long.

Browse: Targets: D · 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

UniProtQ9Y4J8
GeneDTNA
OrganismHomo sapiens
Length743
Binders0
Diseases141
View on UniProt