Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "O"
11 to 20 of 301 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11
Odorant binding protein 2B
LCN14, OBPIIb
Breast cancer, Rheumatoid arthritis, Systemic lupus erythematosus

12
Obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
ARHGEF30, RHABDO1, UNC89
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Dilated cardiomyopathy, Cardiomyopathy, Deafness, Genetic recurrent myoglobinuria, Hepatocellular carcinoma, Hypertrophic cardiomyopathy, Rhabdomyolysis

13
Obscurin like cytoskeletal adaptor 1
-
3m syndrome, Desbuquois syndrome

14
Otoconin 90
PLA2L
Color vision deficiency, Proliferative diabetic retinopathy, Vestibular disease

15
OCA2 melanosomal transmembrane protein
BEY, BEY1, BEY2, BOCA, D15S12, EYCL, EYCL2, EYCL3, HCL3, P, PED, SHEP1, SLC13B1
Amblyopia, Angelman syndrome, Asthma, Attention deficit hyperactivity disorder, Basal cell carcinoma, Eye neoplasms, Biliary tract cancer, Breast cancer, Brown oculocutaneous albinism, Cancer, Cataract, Cervical cancer, Colorectal cancer, Congenital nystagmus, Melanoma
View all (26 more)

16
Occludin/ELL domain containing 1
FWP009, S863-9
Aicardi syndrome

17
OCIA domain containing 1
ASRIJ, OCIA, TPA018
Breast cancer, Rheumatoid arthritis, Diabetes mellitus type 2

18
OCIA domain containing 2
-
Metabolic syndrome, Diabetes mellitus type 2

19
Occludin
BLCPMG, PPP1R115, PTORCH1
Rhinitis, Brain injuries, Breast neoplasms, Congenital microcephaly, Crohn disease, Hypertension, Global developmental delay, Hepatic veno occlusive disease, Kidney failure, Pseudo-torch syndrome, Splenomegaly

20
OCRL inositol polyphosphate-5-phosphatase
DENT2, Dent-2, INPP5F, LOCR, NPHL2, OCRL-1, OCRL1
Congenital cataract, Dent disease, Intellectual developmental disorder, Oculocerebrorenal syndrome