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
Showing genes starting with "C"
361 to 370 of 1806 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
Chromobox 2
CDCA6, M33, SRXY5
46, xy complete gonadal dysgenesis, 46, xy sex reversal, Swyer syndrome

362
Chromobox 4
NBP16, PC2
Major depressive disorder, Osteonecrosis, Rheumatic disease

363
Chromobox 5
HEL25, HP1, HP1A, HP1alpha
Androgenetic alopecia, Colorectal neoplasms, Metabolic syndrome, Diabetes mellitus type 2

364
Chromobox 6
-
Atrial fibrillation, Insomnia, Schizophrenia, Scoliosis, Urinary bladder cancer

365
Chromobox 7
-
Multiple myeloma, Diabetes mellitus type 2

366
Chromobox 8
PC3, RC1
Atrial fibrillation, Attention deficit hyperactivity disorder, Breast cancer, Schizophrenia, Substance abuse

367
Chibby 1, beta catenin antagonist
C22orf2, CBY, Chibby1, HS508I15A, PGEA1, PIGEA-14, PIGEA14, arb1
Ciliopathy, Aplasia of the vermis, Joubert syndrome

368
Chibby family member 2
NURIT, SPERT
Scoliosis

369
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

370
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)