Genes | GeDiPNet - Gene Disease Pathway & Associations

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331 to 340 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
331	100528021	ST20-MTHFS	ST20-MTHFS readthrough	MTHFS	Dysautonomia, Dyscognitive seizures, Epilepsy, Esotropia, Hypotonic seizures, Salaam seizures, Seizure
332	100528030	POC1B-GALNT4	POC1B-GALNT4 readthrough	GALNT4, GalNAc-T4	Schizophrenia
333	100528032	KLRC4-KLRK1	KLRC4-KLRK1 readthrough	-	Behcet syndrome
334	100529063	BCL2L2-PABPN1	BCL2L2-PABPN1 readthrough	-	Oculopharyngeal muscular dystrophy
335	100529097	RPL36A-HNRNPH2	RPL36A-HNRNPH2 readthrough	-	Cardiomyopathy, Fabry disease, Fabry disease, cardiac variant, Hypertrophic cardiomyopathy
336	100529144	CORO7-PAM16	CORO7-PAM16 readthrough	CORO7, Coronin-7, Crn7	Chondrodysplasia punctata, Schizophrenia
337	100529211	TMEM256-PLSCR3	TMEM256-PLSCR3 readthrough (NMD candidate)	C17orf61-PLSCR3, PLSCR3	Asphyxiating thoracic dystrophy, Brachydactyly, Syndactyly of fingers
338	100529239	RPS10-NUDT3	RPS10-NUDT3 readthrough	-	Diamond-blackfan anemia
339	100529240	ZNF816-ZNF321P	ZNF816-ZNF321P readthrough	ZNF816-ZNF321	Psoriasis
340	100529241	HSPE1-MOB4	HSPE1-MOB4 readthrough	HSPE1-PHOCN	Development disorder, Schizophrenia

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