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High affinity choline transporter 1 (SLC5A7)

Homo sapiens — UniProt Q9GZV3

Gene: SLC5A7Homo sapiensSwissProt reviewedTransporter

Data last refreshed: (UniProt release unknown)

Key facts

High affinity choline transporter 1 (SLC5A7) is a protein from Homo sapiens identified by UniProt accession Q9GZV3, 580 residues long. MolForge cross-references it against 1 known binders and 213 disease associations.

  • UniProt accession: Q9GZV3; gene symbol SLC5A7.
  • Organism: Homo sapiens.
  • Length: 580 amino acids.
  • Target class: Transporter.
  • Top disease associations (Open Targets): Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndromes and distal hereditary motor neuropathy type 7.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameHigh affinity choline transporter 1
UniProt accessionQ9GZV3
GeneSLC5A7
OrganismHomo sapiens
Length580 residues
Molecular weight—
EC numbers—
Target classTransporter (inferred from UniProt keywords / EC)
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 (213)

Diseases linked to this target (Open Targets).

  • Presynaptic congenital myasthenic syndromes · score 0.75
  • Congenital myasthenic syndromes · score 0.67
  • distal hereditary motor neuropathy type 7 · score 0.58
  • hereditary motor and sensory neuropathy · score 0.37
  • Charcot-Marie-Tooth disease type 2 · score 0.27
  • genetic disorder · score 0.19
  • cutaneous melanoma · score 0.18
  • malate measurement · score 0.13
  • squamous cell lung carcinoma · score 0.12
  • distal hereditary motor neuropathy · score 0.11

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9GZV3-F1alphafoldPREDICTED84.35—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9GZV3.

Amino-acid sequence (580 residues)

MAFHVEGLIA IIVFYLLILL VGIWAAWRTK NSGSAEERSE AIIVGGRDIG LLVGGFTMTA TWVGGGYING TAEAVYVPGY GLAWAQAPIG YSLSLILGGL FFAKPMRSKG YVTMLDPFQQ IYGKRMGGLL FIPALMGEMF WAAAIFSALG ATISVIIDVD MHISVIISAL IATLYTLVGG LYSVAYTDVV QLFCIFVGLW ISVPFALSHP AVADIGFTAV HAKYQKPWLG TVDSSEVYSW LDSFLLLMLG GIPWQAYFQR VLSSSSATYA QVLSFLAAFG CLVMAIPAIL IGAIGASTDW NQTAYGLPDP KTTEEADMIL PIVLQYLCPV YISFFGLGAV SAAVMSSADS SILSASSMFA RNIYQLSFRQ NASDKEIVWV MRITVFVFGA SATAMALLTK TVYGLWYLSS DLVYIVIFPQ LLCVLFVKGT NTYGAVAGYV SGLFLRITGG EPYLYLQPLI FYPGYYPDDN GIYNQKFPFK TLAMVTSFLT NICISYLAKY LFESGTLPPK LDVFDAVVAR HSEENMDKTI LVKNENIKLD ELALVKPRQS MTLSSTFTNK EAFLDVDSSP EGSGTEDNLQ

Frequently asked questions

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

Which diseases are associated with SLC5A7?

The strongest Open Targets associations for SLC5A7 are Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndromes, distal hereditary motor neuropathy type 7, hereditary motor and sensory neuropathy and Charcot-Marie-Tooth disease type 2.

How long is the SLC5A7 protein?

The Homo sapiens SLC5A7 protein (UniProt Q9GZV3) is 580 amino acids long.

Browse: Targets: S · 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

UniProtQ9GZV3
GeneSLC5A7
OrganismHomo sapiens
Length580
Binders1
Diseases213
View on UniProt