Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
1211 to 1220 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1211
Sperm microtubule inner protein 10
C5orf48, TEX43, Tseg7
Colorectal cancer

1212
Sperm microtubule inner protein 11
LINC00935, TEX49
Lethal congenital contracture syndrome

1213
Sperm microtubule inner protein 2
C4orf45
Alzheimer disease, Attention deficit hyperactivity disorder, Insomnia, Systemic mastocytosis

1214
Sperm microtubule inner protein 3
C1orf100
Asthma, Congenital cardiovascular anomaly, Heart disease, Major depressive disorder, Schizophrenia, Scoliosis, Diabetes mellitus type 2, Uterine fibroid

1215
Sperm microtubule inner protein 5
C10orf82
Coronary artery disease

1216
Sperm microtubule inner protein 7
C7orf72, SPATA48
Alzheimer disease, Ankylosing spondylitis, Asthma, Eczema, Basal cell carcinoma, B-cell acute lymphoblastic leukemia, Color vision deficiency, Crohn disease, Disorder of pharynx, Inflammatory bowel disease, Keratinocyte carcinoma, Major depressive disorder, Multiple sclerosis, Neurotic disorder, Non-melanoma skin carcinoma
View all (9 more)

1217
Sperm microtubule inner protein 8
TEPP
Obstructive pulmonary disease

1218
Sialophorin
CD43, GALGP, GPL115, LEU-22, LSN
Calcinosis, Heart valve disease, Heart valve prolapse

1219
SPNS lysolipid transporter 1, lysophospholipid
HSpin1, LAT, PP2030, SLC62A1, SLC63A1, SPIN1, SPINL, nrs
Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism

1220
SPNS lysolipid transporter 2, sphingosine-1-phosphate
DFNB115, SLC62A2, SLC63A2
Deafness, Hearing impairment, Hearing loss