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
1851 to 1860 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1851
Chromobox 7
-
Multiple myeloma, Diabetes mellitus type 2

1852
Chromobox 8
PC3, RC1
Atrial fibrillation, Attention deficit hyperactivity disorder, Breast cancer, Schizophrenia, Substance abuse

1853
Chibby 1, beta catenin antagonist
C22orf2, CBY, Chibby1, HS508I15A, PGEA1, PIGEA-14, PIGEA14, arb1
Ciliopathy, Aplasia of the vermis, Joubert syndrome

1854
Chibby family member 2
NURIT, SPERT
Scoliosis

1855
Coiled-coil and C2 domain containing 1A
Aki-1, FREUD-1, Freud-1/Aki1, Lgd2, MRT3, TAPE
Autism, Nonsyndromic intellectual disability, Ciliopathy, Neurodevelopmental disorder, Intellectual developmental disorder, Major depressive disorder, Non-specific syndromic intellectual disability, Premature ovarian failure, Depression

1856
Coiled-coil and C2 domain containing 2A
COACH2, JBTS9, MKS6, RP93
Anencephaly, Arima syndrome, Bell's palsy, Central nervous system cancer, Obstructive pulmonary disease, Ciliopathy, Coach syndrome, Color vision deficiency, Conduct disorder, Congenital clubfoot, Cystic kidney disease, Dementia, Desbuquois syndrome, Encephalocele, Endometriosis
View all (17 more)

1857
Coiled-coil and C2 domain containing 2B
C10orf130, C10orf131
Dementia, Diverticular disease

1858
Cell cycle and apoptosis regulator 2
DBC-1, DBC1, KIAA1967, NET35, p30 DBC, p30DBC
Hemorrhoid, Insomnia, Diabetes mellitus type 2, Wallerian degeneration

1859
Collagen and calcium binding EGF domains 1
HKLLS1
Bipolar disorder, Bone remodeling disease, Hepatocellular carcinoma, Corneal ulcer, Eye disease, Hennekam syndrome, Hydrops fetalis, Hypothyroidism, Intellectual developmental disorder, Major depressive disorder, Distal renal tubular acidosis, Schizophrenia

1860
Coiled-coil domain containing 102A
-
Cataract, Diabetes mellitus type 2, Psoriasis