Genesⓘ

Dataset:
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

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

203
Solute carrier family 5 member 8
AIT, SMCT, SMCT1
Colonic neoplasms, Hyperuricemia

204
Stereocilin
DFNB16
Asthenozoospermia, Azoospermia, Deafness, Deafness-infertility syndrome, Hearing loss, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Oligospermia, Sensorineural hearing loss, Spermatogenic failure

205
Sprouty related EVH1 domain containing 1
LGSS, NFLS, PPP1R147, hSpred1, spred-1
Anencephaly, Attention deficit hyperactivity disorder, Cafe-au-lait macules with pulmonary stenosis, Congenital epicanthus, Drachtman weinblatt sitarz syndrome, Dysmorphic features, High palate, Legius syndrome, Macrocephaly, Micrognathism, Multiple congenital anomalies, Multiple lipomata, Neurofibroma, Neurofibromatosis, Ptosis
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206
Solute carrier family 16 member 11
MCT 11, MCT11
Diabetes mellitus

207
Signal peptide peptidase like 2C
IMP5
Alopecia, Alopecia, male pattern, Androgenetic alopecia, Chronic obstructive pulmonary disease, Corticobasal degeneration, Lung diseases, Parkinson disease, Biliary cirrhosis

208
Spectrin repeat containing nuclear envelope family member 4
C19orf46, DFNB76, KASH4, Nesp4
Deafness, Non-syndromic sensorineural deafness, Nonsyndromic deafness

209
SAS-6 centriolar assembly protein
MCPH14, SAS-6, SAS6
Agenesis of corpus callosum, Developmental delay, Dwarfism, Dysmorphic features, Mental retardation, Microcephaly, Neuronal heterotopia, Pachygyria, Renal aplasia, Vesicoureteral reflux

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