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Gigaxonin (GAN)

Homo sapiens — UniProt Q9H2C0

Gene: GANHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Gigaxonin (GAN) is a protein from Homo sapiens identified by UniProt accession Q9H2C0, 597 residues long. MolForge cross-references it against 0 known binders and 323 disease associations.

  • UniProt accession: Q9H2C0; gene symbol GAN.
  • Organism: Homo sapiens.
  • Length: 597 amino acids.
  • Top disease associations (Open Targets): giant axonal neuropathy, genetic disorder and peripheral neuropathy.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameGigaxonin
UniProt accessionQ9H2C0
GeneGAN
OrganismHomo sapiens
Length597 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 (323)

Diseases linked to this target (Open Targets).

  • giant axonal neuropathy · score 0.76
  • genetic disorder · score 0.51
  • peripheral neuropathy · score 0.27
  • Hypotonia · score 0.26
  • Intellectual disability · score 0.26
  • clear cell renal carcinoma · score 0.18
  • Charcot-Marie-Tooth disease · score 0.16
  • neuritic plaque measurement · score 0.11
  • colonic neoplasm · score 0.10
  • anal neoplasm · score 0.10

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H2C0-F1alphafoldPREDICTED89.84—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H2C0.

Amino-acid sequence (597 residues)

MAEGSAVSDP QHAARLLRAL SSFREESRFC DAHLVLDGEE IPVQKNILAA ASPYIRTKLN YNPPKDDGST YKIELEGISV MVMREILDYI FSGQIRLNED TIQDVVQAAD LLLLTDLKTL CCEFLEGCIA AENCIGIRDF ALHYCLHHVH YLATEYLETH FRDVSSTEEF LELSPQKLKE VISLEKLNVG NERYVFEAVI RWIAHDTEIR KVHMKDVMSA LWVSGLDSSY LREQMLNEPL VREIVKECSN IPLSQPQQGE AMLANFKPRG YSECIVTVGG EERVSRKPTA AMRCMCPLYD PNRQLWIELA PLSMPRINHG VLSAEGFLFV FGGQDENKQT LSSGEKYDPD ANTWTALPPM NEARHNFGIV EIDGMLYILG GEDGEKELIS MECYDIYSKT WTKQPDLTMV RKIGCYAAMK KKIYAMGGGS YGKLFESVEC YDPRTQQWTA ICPLKERRFG AVACGVAMEL YVFGGVRSRE DAQGSEMVTC KSEFYHDEFK RWIYLNDQNL CIPASSSFVY GAVPIGASIY VIGDLDTGTN YDYVREFKRS TGTWHHTKPL LPSDLRRTGC AALRIANCKL FRLQLQQGLF RIRVHSP

Frequently asked questions

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

Which diseases are associated with GAN?

The strongest Open Targets associations for GAN are giant axonal neuropathy, genetic disorder, peripheral neuropathy, Hypotonia and Intellectual disability.

How long is the GAN protein?

The Homo sapiens GAN protein (UniProt Q9H2C0) is 597 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

UniProtQ9H2C0
GeneGAN
OrganismHomo sapiens
Length597
Binders0
Diseases323
View on UniProt