Excel File Text File *Disease is associated/modeled with this Gene or a homolog. More...
			Disease Term	Human Homologs	Mouse Homologs	Mouse Models	Homology Source
			Borjeson-Forssman-Lehmann syndrome	PHF6*	Phf6*	2 models	Alliance of Genome Resources
			Christianson syndrome	SLC9A6*	Slc9a6*	3 models	Alliance of Genome Resources
			Renpenning syndrome	PQBP1*	Pqbp1*	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual disability 5	AP1S2*	Ap1s2*	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual disability Claes-Jensen type	KDM5C*	Kdm5c*	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual disability Raymond type	ZDHHC9*	Zdhhc9*	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual disability Siderius type	PHF8*	Phf8*	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual developmental disorder bain type	HNRNPH2	Hnrnph2*	3 models	Alliance of Genome Resources
			syndromic X-linked intellectual disability	RAB39B	Rab39b*	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual disability	ARX	Arx*	1 model	Alliance of Genome Resources
			Armfield syndrome	FAM50A*	Fam50a		Alliance of Genome Resources
			Arts syndrome	PRPS1*	Prps1		Alliance of Genome Resources
			Arts syndrome	PITX2*	Pitx2		Alliance of Genome Resources
			Basilicata-Akhtar syndrome	MSL3*	Msl3		Alliance of Genome Resources
			corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	IGBP1*, IGBP1C	Igbp1		Alliance of Genome Resources
			female-restricted syndromic X-linked intellectual disability 99	USP9X*	Usp9x		Alliance of Genome Resources
			MEHMO syndrome	EIF2S3*, EIF2S3B	Eif2s3x		Alliance of Genome Resources
			Miles-Carpenter syndrome	ZC4H2*	Zc4h2		Alliance of Genome Resources
			Mullegama-Klein-Martinez syndrome	STAG2*	Stag2		Alliance of Genome Resources
			Paganini-Miozzo syndrome	HS6ST2*	Hs6st2		Alliance of Genome Resources
			Partington syndrome	ARX*	Arx		Alliance of Genome Resources
			Prieto syndrome	WNK3*	Wnk3		Alliance of Genome Resources
			Raynaud-Claes syndrome	CLCN4*	Clcn4		Alliance of Genome Resources
			syndromic X-linked intellectual disability	NKAP*	Nkap		Alliance of Genome Resources
			syndromic X-linked intellectual disability	HNRNPH2*	Hnrnph2		Alliance of Genome Resources
			syndromic X-linked intellectual disability	TAF1*, TAF1L	Taf1		Alliance of Genome Resources
			syndromic X-linked intellectual disability	DDX3X*	D1Pas1, Ddx3x		Alliance of Genome Resources
			syndromic X-linked intellectual disability 14	UPF3B*	Upf3b		Alliance of Genome Resources
			syndromic X-linked intellectual disability 34	NONO*	Nono		Alliance of Genome Resources
			syndromic X-linked intellectual disability 94	GRIA3*	Gria3		Alliance of Genome Resources
			syndromic X-linked intellectual disability Cabezas type	CUL4B*	Cul4b		Alliance of Genome Resources
			syndromic X-linked intellectual disability Hedera type	ARX*	Arx		Alliance of Genome Resources
			syndromic X-linked intellectual disability Hedera type	ATP6AP2*	Atp6ap2		Alliance of Genome Resources
			syndromic X-linked intellectual disability Lubs type	MECP2*	Mecp2	1 model	Alliance of Genome Resources
			syndromic X-linked intellectual disability Najm type	CASK*	Cask		Alliance of Genome Resources
			syndromic X-linked intellectual disability Nascimento type	UBE2A*	Ube2a		Alliance of Genome Resources
			syndromic X-linked intellectual disability Pilorge type	GLRA2*	Glra2		Alliance of Genome Resources
			syndromic X-linked intellectual disability Shashi type	RBMX*	Rbmx		Alliance of Genome Resources
			syndromic X-linked intellectual disability Snyder type	SMS*	Sms, Sms-ps		Alliance of Genome Resources
			syndromic X-linked intellectual disability Turner type	HUWE1*	Huwe1		Alliance of Genome Resources
			syndromic X-linked intellectual disability type 10	HSD17B10*	Hsd17b10		Alliance of Genome Resources
			syndromic X-linked intellectual disorder Lujan-Fryns-type	MED12*	Med12		Alliance of Genome Resources
			syndromic X-linked mental retardation 35	RPL10*	Rpl10, Rpl10-ps3		Alliance of Genome Resources
			syndromic X-linked mental retardation Hough type	CNKSR2*	Cnksr2		Alliance of Genome Resources
			Tonne-Kalscheuer syndrome	RLIM*	Rlim		Alliance of Genome Resources
			Van Esch-O'Driscoll syndrome	POLA1*	Pola1		Alliance of Genome Resources
			Wilson-Turner syndrome	LAS1L*	Las1l		Alliance of Genome Resources
			Wilson-Turner syndrome	HDAC8*	Hdac8		Alliance of Genome Resources
			X-linked intellectual developmental disorder 108	SLC9A7*	Slc9a7		Alliance of Genome Resources
			X-linked intellectual developmental disorder 109	AFF2*	Aff2		Alliance of Genome Resources
			X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	CLIC2*
			X-linked intellectual disability-psychosis-macroorchidism syndrome	MECP2*	Mecp2		Alliance of Genome Resources
			X-linked intellectual disability-short stature-overweight syndrome	THOC2*	Thoc2, Thoc2l		Alliance of Genome Resources
			X-linked mental retardation-hypotonic facies syndrome-1	ATRX*	Atrx		Alliance of Genome Resources
			X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance	OPHN1*	Ophn1		Alliance of Genome Resources

	Transgenes and other genome features developed in mice to model this disease.
	Disease Term	Transgenes and Other Genome Features	Mouse Models
	syndromic X-linked intellectual disability Lubs type	Tg(MECP2)3Hzo	1 model
	syndromic X-linked intellectual disability Lubs type	Tg(MECP2)1Hzo	2 models