Genes | GeDiPNet - Gene Disease Pathway & Associations

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12211 to 12220 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
12211	140679	SLC32A1	Solute carrier family 32 member 1	DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12	Anorexia nervosa, Developmental and epileptic encephalopathy, Generalized epilepsy with febrile seizures plus, Seizure, Intellectual developmental disorder, Obesity, Obsessive-compulsive disorder, Willis-ekbom disease, Schizophrenia
12212	9197	SLC33A1	Solute carrier family 33 member 1	ACATN, AT-1, AT1, CCHLND, HPBDS, SPG42	Spastic paraplegia, Cataract, Colorectal cancer, Congenital cataract hearing loss developmental delay syndrome, Dementia, Developmental disability, Global developmental delay, Hearing impairment, Hearing loss, Hypothyroidism, Insomnia, Neurotic disorder, Partial epilepsy, Hereditary spastic paraplegia
12213	6569	SLC34A1	Solute carrier family 34 member 1	FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2	Asthma, Bladder calculus, Bone disease, Kidney and ureter calculus, Kidney disease, Crohn disease, De toni-debre-fanconi syndrome, Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis, Dominant hypophosphatemia with nephrolithiasis or osteoporosis, Fanconi renotubular syndrome, Fanconi syndrome, Hypercalcemia, Idiopathic infantile hypercalcemia, Hypercalciuria, Hypophosphatemic rickets View all (6 more)
12214	10568	SLC34A2	Solute carrier family 34 member 2	NAPI-3B, NAPI-IIb, NPTIIb, NaPi2b, PULAM	Non-small-cell lung carcinoma
12215	142680	SLC34A3	Solute carrier family 34 member 3	HHRH, NPT2C, NPTIIc	Hypophosphatemic rickets, Desbuquois syndrome, Nephrolithiasis
12216	10559	SLC35A1	Solute carrier family 35 member A1	CDG2F, CMPST, CST, hCST	Congenital disorder of glycosylation
12217	7355	SLC35A2	Solute carrier family 35 member A2	CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL	Autism, Congenital disorder of glycosylation, Developmental and epileptic encephalopathy, X-linked complex neurodevelopmental disorder
12218	23443	SLC35A3	Solute carrier family 35 member A3	AMRS	Arthrogryposis multiplex congenita, Arthrogryposis with neurodevelopmental impairment and seizures, Autism, Kidney disease
12219	10237	SLC35B1	Solute carrier family 35 member B1	AXER, UGTREL1	Oligodendroglioma
12220	347734	SLC35B2	Solute carrier family 35 member B2	HLD26, PAPST1, SLL, UGTrel4	Hypomyelinating leukodystrophy

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