Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9341 to 9350 of 15435 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9341
OTU deubiquitinase with linear linkage specificity
AIPDS, AIPDSA, FAM105B, GUM, IMD107
Asthma, Autoinflammation, panniculitis, and dermatosis syndrome, Calcium metabolism disorders, Chondrocalcinosis, Craniometadiaphyseal dysplasia, Craniometaphyseal dysplasia, Immunodeficiency, Diabetes mellitus type 2

9342
OTU deubiquitinase with linear linkage specificity like
FAM105A, NET20
Asthma, Eczema, Obstructive pulmonary disease, Liver cirrhosis, Osteoarthritis, Respiratory system disease, Diabetes mellitus type 2

9343
Orthodenticle homeobox 1
-
Attention deficit hyperactivity disorder, Prostate cancer, Substance abuse, Vesicoureteral reflux

9344
Orthodenticle homeobox 2
CPHD6, MCOPS5
Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Butterfly-shaped pigmentary macular dystrophy, Colobomatous microphthalmia, Combined pituitary hormone deficiency, Desbuquois syndrome, Diabetic neuropathy, Leber congenital amaurosis, Macular dystrophy, Male infertility single gene azoospermia, Medulloblastoma, Microphthalmia
View all (11 more)

9345
Ovochymase 2
OVTN
Contracture, Venous thromboembolism

9346
Ovo like transcriptional repressor 1
HOVO1
Asthma, Eczema, Basal cell carcinoma, Bladder calculus, Breast cancer, Cardiovascular disease, Kidney disease, Atopic dermatitis, Gout, Hypertension, Hypertensive nephropathy, Iga nephropathy, Keratinocyte carcinoma, Kidney failure, Metabolic syndrome
View all (8 more)

9347
Ovo like zinc finger 2
CHED, CHED1, CHED2, EUROIMAGE566589, PPCD1, ZNF339
Alzheimer disease, Congenital hereditary endothelial dystrophy, Corneal dystrophy, Hereditary corneal dystrophy, Peripheral arterial disease, Polymorphous corneal dystrophy, Posterior polymorphous corneal dystrophy

9348
Ovo like zinc finger 3
HOVO3
Atrial fibrillation

9349
OXA1L mitochondrial inner membrane insertase
OXA1, OXA1L1
Mitochondrial disease

9350
3-oxoacid CoA-transferase 1
OXCT, SCOT
Bipolar disorder, Osteoporosis