Genes | GeDiPNet - Gene Disease Pathway & Associations

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12351 to 12360 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
12351	11136	SLC7A9	Solute carrier family 7 member 9	BAT1, CSNU3	Alzheimer disease, Kidney disease, Cystine urolithiasis, Cystinuria, Eosinophilia, Gastroesophageal reflux disease, Gout, Polycystic kidney disease
12352	6546	SLC8A1	Solute carrier family 8 member A1	NCX1	Autoimmune neurological syndrome, Asthma, Bone fracture, Clonal hematopoiesis, Color vision deficiency, Duchenne muscular dystrophy, Hypertension, Myocardial ischemia, Obesity, Periapical periodontitis, Schizophrenia, Seizures, Status epilepticus, Diabetes mellitus type 2
12353	6547	SLC8A3	Solute carrier family 8 member A3	NCX3	Autism, Bipolar disorder, Cystic fibrosis, Dementia, Peripheral arterial disease, Schizophrenia, Scoliosis, Seizures, Status epilepticus
12354	6548	SLC9A1	Solute carrier family 9 member A1	APNH, LIKNS, NHE-1, NHE1, PPP1R143	Barrett esophagus, Cardiomyopathy, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Congestive heart failure, Experimental diabetes, Edema, Heart failure, Hypertrophic cardiomyopathy, Cerebellar ataxia with hearing loss, Ventricular remodeling
12355	6549	SLC9A2	Solute carrier family 9 member A2	NHE2	Asthma, Eczema, Crohn disease, Dissection of aorta, Edema, Endometriosis, Leprosy, Respiratory system disease
12356	6550	SLC9A3	Solute carrier family 9 member A3	DIAR8, NHE-3, NHE3	Autism, Congenital secretory diarrhea, Congenital sodium diarrhea, Cystic fibrosis, Experimental diabetes, Diarrhea, Diverticular disease, Dysentery, Edema, Hypotension, Intestinal obstruction, Lung disease, Schizophrenia
12357	389015	SLC9A4	Solute carrier family 9 member A4	NHE4	Ankylosing spondylitis, Imperforate anus, Asthma, Eczema, Atypical femoral fracture, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Crohn disease, Dissection of aorta, Inflammatory bowel disease, Juvenile idiopathic arthritis, Leprosy, Nasal polyp View all (6 more)
12358	6553	SLC9A5	Solute carrier family 9 member A5	NHE5	Kidney failure
12359	10479	SLC9A6	Solute carrier family 9 member A6	MRSA, MRXSCH, NDPACX, NHE6	Amblyopia, Astigmatism, Christianon syndrome, Global developmental delay, Hyperopia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Leukodystrophy, Neurodegenerative disorder, x-linked, female-restricted, with parkinsonism and cognitive impairment, Neurodevelopmental disorder, Scoliosis, Strabismus
12360	84679	SLC9A7	Solute carrier family 9 member A7	MRX108, NHE-7, NHE7, SLC9A6	Alzheimer disease, Intellectual developmental disorder, x-linked, X-linked intellectual disability

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