gene_symbol,description,uniprot_id,entrez_id,chromosomal_location
MAOA,"monoamine oxidase A ",P21397,4128,"chrX: 43,654,907-43,746,824"
ATRX,"alpha thalassemia/mental retardation syndrome X-linked ",P46100,546,"chrX: 77,504,878-77,786,269"
SLC6A8,"solute carrier family 6 (neurotransmitter transporter), member 8 ",P48029,6535,"chrX: 153,688,099-153,696,593"
CASK,"calcium/calmodulin-dependent serine protein kinase (MAGUK family) ",O14936,8573,"chrX: 41,514,934-41,923,463"
PQBP1,"polyglutamine binding protein 1 ",O60828,10084,"chrX: 48,897,912-48,903,143"
PCDH19,"protocadherin 19 ",Q8TAB3,57526,"chrX: 100,291,644-100,410,273"
RAB39B,"RAB39B, member RAS oncogene family ",Q96DA2,116442,"chrX: 155,258,241-155,264,589"
AGTR2,"angiotensin II receptor, type 2 ",P50052,186,"chrX: 116,170,722-116,174,972"
PTCHD1,"patched domain containing 1 ",Q96NR3,139411,"chrX: 23,334,016-23,404,372"
GDI1,"GDP dissociation inhibitor 1 ",P31150,2664,"chrX: 154,436,913-154,443,467"