Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12661 to 12670 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12661
Spermatogenesis associated 7
HEL-S-296, HSD-3.1, HSD3, LCA3, RP94
Attention deficit hyperactivity disorder, Retinitis pigmentosa, Central nervous system cancer, Glioblastoma, Glioma, Leber congenital amaurosis, Optic atrophy, Stargardt disease

12662
Spermatogenesis associated 9
NYD-SP16
Obstructive pulmonary disease

12663
Spermatogenesis and centriole associated 1
SPATA15
Alzheimer disease, Crohn disease, Dementia, Gastroesophageal reflux disease, Inflammatory bowel disease

12664
Spermatogenesis and centriole associated 1 like
C21orf56
Laryngitis, Hearing impairment, Hearing loss

12665
Spermatogenesis associated serine rich 1
DDIP, SPATA8, SRSP1
Alzheimer disease, Ovarian cancer, Visual impairment

12666
Spermatogenesis associated serine rich 2
Nbla00526, P59SCR, SCR59, SPATA10
Alzheimer disease

12667
Spermatogenesis associated serine rich 2 like
DNAPTP6, SGNP
Aortic disease, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Bipolar disorder, Obstructive pulmonary disease, Crohn disease, Dilated cardiomyopathy, Esophageal disease, Esophageal ulcer, Heart failure, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Insomnia, Metabolic syndrome
View all (4 more)

12668
SPC24 component of NDC80 kinetochore complex
SPBC24
Carpal tunnel syndrome, Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Hemorrhoid, Myocardial infarction, Rheumatoid arthritis

12669
SPC25 component of NDC80 kinetochore complex
AD024, SPBC25, hSpc25
Carbohydrate metabolism disease, Hepatocellular carcinoma, Gestational diabetes, Intestinal disaccharide malabsorption, Metabolic syndrome, Osteoarthritis, Diabetes mellitus type 2

12670
Signal peptidase complex subunit 1
HSPC033, SPC1, SPC12, YJR010C-A
Attention deficit hyperactivity disorder, Autism