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MIRAGE
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)

Summary
Species
Homo sapiens
Reactome
PubChem
Click on a node on the pathway to see its details. Glycoproteins are marked with a glycoprotein icon in their name.
SPV: a JavaScript Signaling Pathway Visualizer, Bioinformatics, 2018
Displaying 1 entry
UniProt ID Protein Name Gene Symbol Pathway Viewer
Q9GZV3 High affinity choline transporter 1
  • CHT1
  • SLC5A7
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025