Uniprot AC	Entrez ID	Gene Name	Disease	Cell Type	PTM Type	State	Position	PMID
Q6ZUT3	90167	FRMD7	autosomal recessive congenital nystagmus		Phosphorylation	N	S260	
Q6ZUT3	90167	FRMD7	autosomal recessive congenital nystagmus		Ubiquitination	N	K295	
Q6ZUT3	90167	FRMD7	Adrenocortical carcinoma		Phosphorylation	N	S298	
Q6ZUT3	90167	FRMD7	Brain lower grade glioma		Phosphorylation	N	S298	
Q6ZUT3	90167	FRMD7	Glioblastoma multiforme		Phosphorylation	N	S298	
Q6ZUT3	90167	FRMD7	Infantile nystagmus		Phosphorylation	N	S298	
Q6ZUT3	90167	FRMD7	Skin cutaneous melanoma		Phosphorylation	N	S298	
Q6ZUT3	90167	FRMD7	autosomal recessive congenital nystagmus		Phosphorylation	N	S298	
Q6ZUT3	90167	FRMD7	Adrenocortical carcinoma		Phosphorylation	N	S302	
Q6ZUT3	90167	FRMD7	Brain lower grade glioma		Phosphorylation	N	S302	
Q6ZUT3	90167	FRMD7	Glioblastoma multiforme		Phosphorylation	N	S302	
Q6ZUT3	90167	FRMD7	Infantile nystagmus		Phosphorylation	N	S302	
Q6ZUT3	90167	FRMD7	Skin cutaneous melanoma		Phosphorylation	N	S302	
Q6ZUT3	90167	FRMD7	autosomal recessive congenital nystagmus		Phosphorylation	N	S302	
Q6ZUT3	90167	FRMD7	Glioblastoma multiforme		Phosphorylation	N	S592	
Q6ZUT3	90167	FRMD7	Glioblastoma multiforme		Phosphorylation	N	S605	
Q6ZUT3	90167	FRMD7	Head and neck squamous cell carcinoma		Phosphorylation	N	S605	
Q6ZUT3	90167	FRMD7	Infantile nystagmus		Phosphorylation	N	S605