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
2701 to 2710 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2701
Cyclic nucleotide gated channel subunit alpha 4
CNCA2, CNG-4, CNG4, CNG5, CNGB2, OCNC2, OCNCBETA, OCNCb
Duodenal ulcer, Gastric ulcer, Gastroesophageal reflux disease, Peptic ulcer disease

2702
Cyclic nucleotide gated channel subunit beta 1
CNCG2, CNCG3L, CNCG4, CNG4, CNGB1B, GAR1, GARP, GARP2, RCNC2, RCNCb, RCNCbeta, RP45
Alzheimer disease, Amblyopia, Retinitis pigmentosa, Dementia, Optic atrophy, Peripheral neuropathy

2703
Cyclic nucleotide gated channel subunit beta 3
ACHM1
Achromatopsia, Anxiety disorder, Color vision deficiency, Cone dystrophy, Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Metabolic syndrome, Nystagmus, Optic atrophy, Retinitis pigmentosa, Stargardt disease, Diabetes mellitus type 2

2704
Cornichon family member 1
CNIH, CNIH-1, CNIL, TGAM77
Colorectal cancer

2705
Cornichon family AMPA receptor auxiliary protein 2
CNIH-2, Cnil
Gout, Insomnia

2706
Cornichon family AMPA receptor auxiliary protein 3
CNIH-3
Central nervous system cancer, Endometriosis, Glioblastoma, Glioma, Osteoarthritis, Schizophrenia

2707
Cornichon family member 4
CNIH-4, HSPC163
Major depressive disorder

2708
Connector enhancer of kinase suppressor of Ras 1
CNK, CNK1
Intellectual developmental disorder, Neurodevelopmental disorder

2709
Connector enhancer of kinase suppressor of Ras 2
CNK2, KSR2, MAGUIN, MRXSHG
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Diabetes mellitus type 2, Insomnia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, X-linked intellectual disability, Post-traumatic stress disorder, Psychiatric disorders, Schizophrenia, X-linked complex neurodevelopmental disorder

2710
CNKSR family member 3
CNK3, CNK3/IPCEF1, MAGI1
Color vision deficiency, Osteonecrosis of the femoral head, Parkinson disease