Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12571 to 12580 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12571
Sperm associated antigen 6
CFAP194, CT141, FAP194, Repro-SA-1, pf16
Alzheimer disease, Breast cancer, Differentiated thyroid carcinoma

12572
Sperm associated antigen 8
BS-84, CILD28, CT142, HSD-1, SMP1, SPAG3, hSMP-1
Colorectal cancer, Familial focal epilepsy with variable foci

12573
Sperm associated antigen 9
CT89, HLC-6, HLC4, HLC6, JIP-4, JIP4, JLP, PHET, PIG6
Liver cirrhosis, Myocardial infarction, Schizophrenia

12574
Sperm adhesion molecule 1
HEL-S-96n, HYA1, HYAL1, HYAL3, HYAL5, PH-20, PH20, SPAG15
Atrial fibrillation, Atrial flutter

12575
SPANX family member N1
CT11.6
Chromosome xq28 duplication syndrome

12576
SPANX family member N3
CT11.8, SPANX-N3
Uterine fibroid

12577
SPANX family member N4
CT11.9
Chondromalacia, Conotruncal cardiac defect, Major depressive disorder, Mood disorder, Prostate cancer

12578
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)

12579
SPARC like 1
MAST 9, MAST9, PIG33, SC1
Congenital stromal corneal dystrophy, Corneal dystrophy, Endometriosis, Epilepsy, Esophageal adenocarcinoma, Gout

12580
Spartin
SPG20, TAHCCP1
Spastic paraplegia, Cerebellar ataxia, Dysarthria, Eye disease, Global developmental delay, Hereditary spastic paraplegia, Strabismus, Troyer syndrome