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Ganglioside-induced differentiation-associated protein 2 (GDAP2)

Homo sapiens — UniProt Q9NXN4

Gene: GDAP2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Ganglioside-induced differentiation-associated protein 2 (GDAP2) is a protein from Homo sapiens identified by UniProt accession Q9NXN4, 497 residues long. MolForge cross-references it against 0 known binders and 22 disease associations.

  • UniProt accession: Q9NXN4; gene symbol GDAP2.
  • Organism: Homo sapiens.
  • Length: 497 amino acids.
  • Top disease associations (Open Targets): spinocerebellar ataxia, autosomal recessive, 27, Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome and reticulocyte count.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameGanglioside-induced differentiation-associated protein 2
UniProt accessionQ9NXN4
GeneGDAP2
OrganismHomo sapiens
Length497 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).

  • spinocerebellar ataxia, autosomal recessive, 27 · score 0.57
  • Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome · score 0.18
  • reticulocyte count · score 0.18
  • myeloid white cell count · score 0.05
  • age-related hearing impairment · score 0.05
  • mean corpuscular hemoglobin concentration · score 0.04
  • mean corpuscular volume · score 0.04
  • Red cell distribution width · score 0.03
  • mean corpuscular hemoglobin · score 0.03
  • body height · score 0.02

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NXN4-F1alphafoldPREDICTED82.06—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NXN4.

Amino-acid sequence (497 residues)

MDPLGAPSQF VDVDTLPSWG DSCQDELNSS DTTAEIFQED TVRSPFLYNK DVNGKVVLWK GDVALLNCTA IVNTSNESLT DKNPVSESIF MLAGPDLKED LQKLKGCRTG EAKLTKGFNL AARFIIHTVG PKYKSRYRTA AESSLYSCYR NVLQLAKEQS MSSVGFCVIN SAKRGYPLED ATHIALRTVR RFLEIHGETI EKVVFAVSDL EEGTYQKLLP LYFPRSLKEE NRSLPYLPAD IGNAEGEPVV PERQIRISEK PGAPEDNQEE EDEGLGVDLS FIGSHAFARM EGDIDKQRKL ILQGQLSEAA LQKQHQRNYN RWLCQARSED LSDIASLKAL YQTGVDNCGR TVMVVVGRNI PVTLIDMDKA LLYFIHVMDH IAVKEYVLVY FHTLTSEYNH LDSDFLKKLY DVVDVKYKRN LKAVYFVHPT FRSKVSTWFF TTFSVSGLKD KIHHVDSLHQ LFSAISPEQI DFPPFVLEYD ARENGPYYTS YPPSPDL

Frequently asked questions

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

Which diseases are associated with GDAP2?

The strongest Open Targets associations for GDAP2 are spinocerebellar ataxia, autosomal recessive, 27, Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome, reticulocyte count, myeloid white cell count and age-related hearing impairment.

How long is the GDAP2 protein?

The Homo sapiens GDAP2 protein (UniProt Q9NXN4) is 497 amino acids long.

Browse: Targets: G · 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

UniProtQ9NXN4
GeneGDAP2
OrganismHomo sapiens
Length497
Binders0
Diseases22
View on UniProt