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
9041 to 9050 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9041
OCIA domain containing 2
-
Metabolic syndrome, Diabetes mellitus type 2

9042
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

9043
OCRL inositol polyphosphate-5-phosphatase
DENT2, Dent-2, INPP5F, LOCR, NPHL2, OCRL-1, OCRL1
Congenital cataract, Dent disease, Intellectual developmental disorder, Oculocerebrorenal syndrome

9044
Osteoclast stimulatory transmembrane protein
C20orf123, OC-STAMP, dJ257E24.3
Alzheimer disease, Dementia

9045
Outer dynein arm docking complex subunit 1
CCDC114, CILD20
Autism, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Fraser syndrome, Tetralogy of fallot

9046
Outer dynein arm docking complex subunit 2
ARMC4, CILD23, gudu
Autism, Cardiovascular disease, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Hypertension, Male infertility, Obesity, Prostate cancer, Retinal detachment

9047
Outer dynein arm docking complex subunit 3
CCDC151, CILD30, ODA10
Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Congenital nasopharyngeal atresia

9048
Outer dynein arm docking complex subunit 4
TTC25
Ciliary dyskinesia, Situs ambiguus

9049
Odontogenesis associated phosphoprotein
AI2A4, C4orf26
Amelogenesis imperfecta, Dentin dysplasia, Dentinogenesis imperfecta, Hypomaturation amelogenesis imperfecta, Parkinson disease, Diabetes mellitus type 2

9050
Ornithine decarboxylase 1
BABS, NEDBA, NEDBIA, ODC
Colonic neoplasms, Colorectal neoplasms, Global developmental delay, Neurodevelopmental disorder, Papilloma, Skin neoplasms