Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9051 to 9060 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9051
Outer dense fiber of sperm tails 1
CT133, HSPB10, ODF, ODF2, ODF27, ODFP, ODFPG, ODFPGA, ODFPGB, RT7, SODF
Lymphocytic leukemia, Colorectal cancer, Colonic neoplasms, Gout

9052
Outer dense fiber of sperm tails 4
CT134, CT136, OPPO1
Male infertility single gene azoospermia, Uterine fibroid

9053
Odr-4 GPCR localization factor homolog
C1orf27, TTG1, odr-4
Scoliosis

9054
OFD1 centriole and centriolar satellite protein
71-7A, CXorf5, JBTS10, RP23, SGBS2
Bifid nail, Congenital anomalies of the kidney and urinary tract, Ciliary dyskinesia, Ciliopathy, Coach syndrome, Connective tissue disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Orofaciodigital syndrome, Osteoporosis, Otopalatodigital syndrome, Polydactyly, Polymicrogyria, Retinitis pigmentosa
View all (3 more)

9055
O-GlcNAcase
MEA5, MGEA5, NCOAT
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Epilepsy, Generalized epilepsy, Partial epilepsy

9056
Oxoglutarate dehydrogenase
AKGDH, E1k, E1o, HsOGDH, KGD1, OGDC, OGDH-E1, OGDH2, OGDHD
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Lung cancer, Metabolic syndrome, Diabetes mellitus type 2

9057
Oxoglutarate dehydrogenase L
YOBELN
Congestive heart failure, Major depressive disorder, Heart failure, Yoon-bellen neurodevelopmental syndrome

9058
2-oxoglutarate and iron dependent oxygenase domain containing 1
TPA1
Bardet-biedl syndrome, Insomnia, Retinitis pigmentosa

9059
8-oxoguanine DNA glycosylase
HMMH, HOGG1, MUTM, OGH1
Brain disease, Renal cell carcinoma, Discoid lupus erythematosus, Ischemic heart disease, Coronary artery disease, Dermatologic disorder, Developmental coordination disorder, Diabetes mellitus type 2, Esophageal squamous cell carcinoma, Genetic predisposition to disease, Graves disease, Heart disease, Huntington disease, Hyperplasia, Hypertension
View all (12 more)

9060
O-linked N-acetylglucosamine (GlcNAc) transferase
HINCUT-1, HRNT1, MRX106, O-GLCNAC, OGT1, XLID106
Intellectual developmental disorder, x-linked