Gene table: search width pubmed_id = 32077526


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Hereditary peripheral neuropathy (CMT ?) - (AD)
14.138
32077526
SLC9A3R1 (17q25.1)
Solute carrier family 9, member 3, regulator 1
* Hereditary peripheral neuropathy