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"
1121 to 1130 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1121
Sperm associated antigen 6
CFAP194, CT141, FAP194, Repro-SA-1, pf16
Alzheimer disease, Breast cancer, Differentiated thyroid carcinoma

1122
Sperm associated antigen 8
BS-84, CILD28, CT142, HSD-1, SMP1, SPAG3, hSMP-1
Colorectal cancer, Familial focal epilepsy with variable foci

1123
Sperm associated antigen 9
CT89, HLC-6, HLC4, HLC6, JIP-4, JIP4, JLP, PHET, PIG6
Liver cirrhosis, Myocardial infarction, Schizophrenia

1124
Sperm adhesion molecule 1
HEL-S-96n, HYA1, HYAL1, HYAL3, HYAL5, PH-20, PH20, SPAG15
Atrial fibrillation, Atrial flutter

1125
SPANX family member N1
CT11.6
Chromosome xq28 duplication syndrome

1126
SPANX family member N3
CT11.8, SPANX-N3
Uterine fibroid

1127
SPANX family member N4
CT11.9
Chondromalacia, Conotruncal cardiac defect, Major depressive disorder, Mood disorder, Prostate cancer

1128
Secreted protein acidic and cysteine rich
BM-40, OI17, ON, ONT
Bone fragility with contractures, arterial rupture, and deafness, Carcinogenesis, Cervical disc degenerative disorder, Colonic neoplasms, Colorectal neoplasms, Desbuquois syndrome, Hyperalgesia, Intervertebral disc disease, Kidney disease, Myeloid leukemia, Liver cirrhosis, Multiple myeloma, Myocardial ischemia, Necrosis, Osteogenesis imperfecta
View all (5 more)

1129
SPARC like 1
MAST 9, MAST9, PIG33, SC1
Congenital stromal corneal dystrophy, Corneal dystrophy, Endometriosis, Epilepsy, Esophageal adenocarcinoma, Gout

1130
Spartin
SPG20, TAHCCP1
Spastic paraplegia, Cerebellar ataxia, Dysarthria, Eye disease, Global developmental delay, Hereditary spastic paraplegia, Strabismus, Troyer syndrome