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
10181 to 10190 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10181
POM121 transmembrane nucleoporin C
POM121-2
Atrial fibrillation, Hypertension, Heart failure, Metabolic syndrome, Obesity, Osteoarthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 2

10182
POM121 transmembrane nucleoporin like 12
-
Attention deficit hyperactivity disorder, Color vision deficiency, Tourette syndrome, Pelvic organ prolapse, Psoriasis, Substance abuse

10183
POM121 transmembrane nucleoporin like 2
POM121-L, POM121L
Angioedema, Asthma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Obstructive pulmonary disease, Inflammatory bowel disease, Insomnia, Lung cancer, Major depressive disorder, Neurotic disorder, Psoriasis, Rheumatoid arthritis, Schizophrenia, Diabetes mellitus type 1

10184
Proopiomelanocortin
ACTH, CLIP, LPH, MSH, NPP, OBAIRH, POC
Amnesia, Aortic stenosis, Gouty arthritis, Autism, Bipolar disorder, Body weight, Bradycardia, Calcinosis, Renal cell carcinoma, Cardiomegaly, Cardiomyopathy, Catalepsy, Cerebral hemorrhage, Cerebral palsy, Cholelithiasis
View all (66 more)

10185
Protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
GNTI.2, GnT I.2, LGMD2O, LGMDR15, MEB, MGAT1.2, RP76, gnT-I.2
Autism, Limb girdle muscular dystrophy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital neurologic anomalies, Hydrocephalus, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease, Muscular dystrophy, Optic atrophy, Retinitis pigmentosa, Walker-warburg syndrome

10186
Protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)
AGO61, C3orf39, GTDC2, MDDGA8, MDDGC8
Attention deficit hyperactivity disorder, Bipolar disorder, Insomnia, Major depressive disorder, Muscle eye brain disease, Obesity, Post-traumatic stress disorder, Schizophrenia, Substance abuse, Walker-warburg syndrome

10187
Protein O-mannose kinase
MDDGA12, MDDGC12, SGK196
Congenital muscular dystrophy, Limb-girdle muscular dystrophy, Muscle eye brain disease, Walker-warburg syndrome

10188
Proteasome maturation protein
C13orf12, HSPC014, PNAS-110, PRAAS2, UMP1
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome, Proteasome associated autoinflammatory syndrome, Scoliosis

10189
Protein O-mannosyltransferase 1
LGMD2K, LGMDR11, MDDGA1, MDDGB1, MDDGC1, RT
Autism, Limb girdle muscular dystrophy, Cardiomyopathy, Cerebellar ataxia, Cleft lip, Complete unilateral cleft lip, Congenital muscular dystrophy, Congenital neurologic anomalies, Pyridoxine dependent epilepsy, Hearing impairment, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease
View all (3 more)

10190
Protein O-mannosyltransferase 2
LGMD2N, LGMDR14, MDDGA2, MDDGB2, MDDGC2
Autism, Limb girdle muscular dystrophy, Congenital muscular dystrophy, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease, Muscular dystrophy, Walker-warburg syndrome