Gene table: search width pubmed_id = 32220290


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

protein
All allelic disease phenotypes - locus/disease symbols
Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy and Epilepsy - (AR)
13.109
32220290
PIGK (1p31.1)
Phosphatidylinositol Glycan Anchor Biosynthesis Class K Protein
* Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy and Epilepsy - NEDHCAS