Genes | GeDiPNet - Gene Disease Pathway & Associations

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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

9081 to 9090 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
9081	4976	OPA1	OPA1 mitochondrial dynamin like GTPase	BERHS, MGM1, MTDPS14, NPG, NTG, largeG	Auditory neuropathy, Cerebellar ataxia, Optic atrophy, Blepharoptosis, Centronuclear myopathy, Cone-rod dystrophy, Dental caries, Dominant hereditary optic atrophy, Glaucoma, Leigh syndrome, Major depressive disorder, Mitochondrial disease, Mitochondrial dna depletion syndrome, Neurodevelopmental disorder, Osteoarthritis View all (5 more)
9082	80207	OPA3	Outer mitochondrial membrane lipid metabolism regulator OPA3	MGA3	3-methylglutaconic aciduria, Alzheimer disease, Optic atrophy, Costeff optic atrophy syndrome, Retinitis pigmentosa
9083	93377	OPALIN	Oligodendrocytic myelin paranodal and inner loop protein	HTMP10, TMEM10, TMP10	Dementia
9084	4978	OPCML	Opioid binding protein/cell adhesion molecule like	IGLON1, OBCAM, OPCM	Androgenetic alopecia, Anorexia nervosa, Attention deficit hyperactivity disorder, Cardiomyopathy, Colorectal cancer, Coronary artery disease, Crohn disease, Developmental dysplasia of the hip, Diverticular disease, Eating disorder, Gastric cancer, Major depressive disorder, Metabolic syndrome, Migraine, Oligodendroglioma View all (12 more)
9085	4983	OPHN1	Oligophrenin 1	ARHGAP41, MRX60, MRXSBL, OPN1	Androgenetic alopecia, Autism, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital neurologic anomalies, Coronary artery disease, Craniofrontonasal dysplasia, Gross motor development delay, Hypogonadism, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Nystagmus, Prostate cancer, X-linked intellectual disability
9086	26873	OPLAH	5-oxoprolinase, ATP-hydrolysing	5-Opase, OPLA, OPLAHD	5-oxoprolinase deficiency, Alzheimer disease, Atrial fibrillation, Atrial flutter
9087	5956	OPN1LW	Opsin 1, long wave sensitive	CBBM, CBP, COD5, RCP, ROP	Blue cone monochromatism, Color vision deficiency, Cone monochromatism, Cone-rod dystrophy, X-linked cone dysfunction syndrome with myopia
9088	2652	OPN1MW	Opsin 1, medium wave sensitive	CBBM, CBD, COD5, GCP, GOP, OPN1MW1	Blue cone monochromatism, Color vision deficiency, Cone dystrophy, x-linked, Cone monochromatism, Cone-rod dystrophy, Deuteranomaly, X-linked cone dysfunction syndrome with myopia
9089	728458	OPN1MW2	Opsin 1, medium wave sensitive 2	GOP	Deuteranomaly
9090	611	OPN1SW	Opsin 1, short wave sensitive	BCP, BOP, CBT	Atrial fibrillation, Blue cone monochromatism, Cardioembolic stroke, Color vision deficiency, Hodgkin lymphoma, Hypertrophic cardiomyopathy, Retinitis pigmentosa, Systemic lupus erythematosus, Tritanopia

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