Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
201 to 210 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
Shortage in chiasmata 1
C9orf84, MZIP2, SPGF75, ZIP2, ZIP2H
Coronary artery disease, Lung cancer, Male infertility, Male infertility single gene azoospermia, Spermatogenic failure, Testicular azoospermia

202
Solute carrier family 5 member 12
SMCT2
Asthma, Dental caries, Erectile dysfunction

203
Solute carrier family 5 member 8
AIT, SMCT, SMCT1
Colonic neoplasm, Colorectal cancer, Hyperuricemia

204
Stereocilin
DFNB16
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Deafness, sensorineural, and male infertility, Deafness-infertility syndrome, Hearing impairment, Hearing loss, Spermatogenic failure, Diabetes mellitus, type 2

205
Sprouty related EVH1 domain containing 1
LGSS, NFLS, PPP1R147, hSpred1, spred-1
Cafe-au-lait spots, Congenital neurologic anomalies , Costello syndrome, Desbuquois syndrome, Male infertility spermatogenesis disorder, Neurofibromatosis, Neurofibromatosis-noonan syndrome, Noonan syndrome, Psychotic disorders, Scoliosis

206
Solute carrier family 16 member 11
MCT 11, MCT11
Crohn disease, Diabetes mellitus, Diabetic ketoacidosis, Inflammatory bowel disease, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Ulcerative colitis

207
Signal peptide peptidase like 2C
IMP5
Alzheimer disease, Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Parkinson disease

208
Spectrin repeat containing nuclear envelope family member 4
C19orf46, DFNB76, KASH4, Nesp4
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing loss, Nonsyndromic hearing loss

209
SAS-6 centriolar assembly protein
MCPH14, SAS-6, SAS6
Primary microcephaly, Microcephaly

210
Serine palmitoyltransferase small subunit B
ADMP, C3orf57, SSSPTB
Parkinson disease