Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1071 to 1080 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1071	84679	SLC9A7	Solute carrier family 9 member A7	MRX108, NHE-7, NHE7, SLC9A6	Attention deficit hyperactivity disorder, Autism, Camptodactyly of fingers, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Obesity, Seizure, Strabismus, Syndactyly of the toes
1072	84690	SPATA22	Spermatogenesis associated 22	NYD-SP20, NYDSP20, POF25, SPGF96	Canavan disease, Myopia
1073	8470	SORBS2	Sorbin and SH3 domain containing 2	ARGBP2, PRO0618	Arthritis
1074	84727	SPSB2	SplA/ryanodine receptor domain and SOCS box containing 2	GRCC9, SSB2	Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Corneal astigmatism
1075	8482	SEMA7A	Semaphorin 7A (JohnMiltonHagen blood group)	CD108, CDw108, H-SEMA-K1, H-Sema-L, JMH, PFIC11, SEMAK1, SEMAL	Congenital hypogonadotropic hypogonadism
1076	84888	SPPL2A	Signal peptide peptidase like 2A	IMD86, IMP3, PSL2	Alzheimer disease
1077	84889	SLC7A3	Solute carrier family 7 member 3	ATRC3, CAT-3, CAT3	Uterine fibroids, Plexiform leiomyoma
1078	84925	SLC49A4	Solute carrier family 49 member 4	DIRC2, RCC4	Chromophobe carcinoma, Hereditary renal carcinoma, Papillary renal carcinoma, Renal carcinoma
1079	84947	SERAC1	Serine active site containing 1	-	3-methylglutaconic aciduria with sensorineural deafness, encephalopathy and leigh-like syndrome, Blood coagulation disorders, Brain atrophy, Cerebellar atrophy, Cerebral atrophy, Deafness, Developmental delay, Developmental regression, Epileptic encephalopathy, Hearing loss, Hypoglycemia, Lesions in the basal ganglia, Lipid metabolism, inborn errors, Megdel syndrome, Mental retardation, Narcolepsy, Optic atrophy View all (2 more)
1080	85358	SHANK3	SH3 and multiple ankyrin repeat domains 3	DEL22q13.3, PROSAP2, PSAP2, SCZD15, SPANK-2	22q13.3 deletion syndrome, Agenesis of corpus callosum, Arachnoid cyst, Atrial septal defect, Auditory processing disorder, Autism, Autism spectrum disorder, Camptodactyly of fingers, Cerebellar cortical atrophy, Congenital epicanthus, Congenital exomphalos, Development disorder, Developmental delay, Dolichocephaly, Gastroesophageal reflux disease View all (24 more)

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