Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12641 to 12650 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12641
Spermatogenesis associated 13
ARHGEF29, ASEF2
Alzheimer disease, Autoimmune disease, Autoimmune thyroid disease, B-cell acute lymphoblastic leukemia, Central nervous system cancer, Dementia, Estrogen-receptor negative breast cancer, Glioblastoma, Glioma, Hypothyroidism, Orofacial cleft, Peripheral arterial disease, Primary angle closure glaucoma, Squamous cell carcinoma, Thyroid disease
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12642
Spermatogenesis associated 16
NYD-SP12, SPGF6
Asthma, Insomnia, Irritable bowel syndrome, Major depressive disorder, Male infertility globozoospermia, Male infertility round headed spermatozoa, Metabolic syndrome, Osteoarthritis, Spermatogenic failure, Teratozoospermia, Diabetes mellitus type 2

12643
Spermatogenesis associated 17
CFAP305, FAP305, IQCH, MOT17, MSRG-11, MSRG11
Gastric cancer, Schizophrenia

12644
Spermatogenesis associated 18
Mieap, SPETEX1
Breast neoplasms, Coronary artery disease, Osteonecrosis of the femoral head, Metabolic syndrome, Prostatic neoplasms, Squamous cell carcinoma, Diabetes mellitus type 2, Uterine fibroid

12645
Spermatogenesis associated 19
CT132, SPAS1, spergen1
Color vision deficiency, Hyperopia, Insomnia, Metabolic syndrome, Migraine, Parkinson disease, Schizophrenia, Diabetes mellitus type 2

12646
Spermatogenesis associated 2
PD1, PPP1R145, tamo
Coronary artery disease, Psoriasis, Psoriasis vulgaris

12647
Spermatogenesis associated 21
spergen-2, spergen2
Alzheimer disease, Colorectal cancer, Liver neoplasms, Myocardial infarction, Polycystic ovary syndrome

12648
Spermatogenesis associated 22
NYD-SP20, NYDSP20, POF25, SPGF96
Autism, Canavan disease, Color vision deficiency, Fraser syndrome, Genetic infertility, Infertility, Intellectual developmental disorder, Olmsted syndrome, Premature ovarian failure, Spermatogenic failure

12649
Spermatogenesis associated 24
CCDC161, T6441
Hypertrophic cardiomyopathy, Keratoconus

12650
Spermatogenesis associated 3
TSARG1
Alzheimer disease, Dementia, Male infertility single gene azoospermia