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
12581 to 12590 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12581
Spastin
ADPSP, FSP2, SPG4
Atypical femoral fracture, Spastic paraplegia, Cerebral palsy, Littles disease, Neurodevelopmental disorder, Spastic ataxia, Spastic paraplegia, x-linked, Hereditary spastic paraplegia, Hypertension

12582
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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12583
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

12584
Spermatogenesis associated 17
CFAP305, FAP305, IQCH, MOT17, MSRG-11, MSRG11
Gastric cancer, Schizophrenia

12585
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

12586
Spermatogenesis associated 19
CT132, SPAS1, spergen1
Color vision deficiency, Hyperopia, Insomnia, Metabolic syndrome, Migraine, Parkinson disease, Schizophrenia, Diabetes mellitus type 2

12587
Spermatogenesis associated 2
PD1, PPP1R145, tamo
Coronary artery disease, Psoriasis, Psoriasis vulgaris

12588
Spermatogenesis associated 21
spergen-2, spergen2
Alzheimer disease, Colorectal cancer, Liver neoplasms, Myocardial infarction, Polycystic ovary syndrome

12589
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

12590
Spermatogenesis associated 24
CCDC161, T6441
Hypertrophic cardiomyopathy, Keratoconus