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"
541 to 550 of 1796 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

541
C-C motif chemokine receptor 8
CC-CKR-8, CCR-8, CDw198, CKRL1, CMKBR8, CMKBRL2, CY6, GPRCY6, TER1
Hypothyroidism, Status epilepticus

542
C-C motif chemokine receptor 9
CC-CKR-9, CDw199, GPR-9-6, GPR28
Bardet-biedl syndrome, Hypersensitivity, Osteoarthritis, Status epilepticus

543
C-C motif chemokine receptor like 2
ACKR5, CKRX, CRAM, CRAM-A, CRAM-B, HCR
Alzheimer disease, Crohn disease, Dermatologic disorder, Inflammatory bowel disease, Non-melanoma skin carcinoma, Rheumatoid arthritis, Skin disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

544
Copper chaperone for superoxide dismutase
-
Amyotrophic lateral sclerosis, Carpal tunnel syndrome, Copper metabolism disorder, Major depressive disorder

545
Coiled-coil serine rich protein 1
FAM190A
Astrocytoma, Breast cancer, Central nervous system cancer, Kidney disease, Color vision deficiency, Colorectal cancer, Diabetes mellitus, Glioblastoma, Glioma, Hodgkin lymphoma, Insomnia, Lung cancer, Major depressive disorder, Metabolic syndrome, Multiple myeloma
View all (9 more)

546
Chaperonin containing TCP1 subunit 2
99D8.1, CCT-beta, CCTB, HEL-S-100n, PRO1633, TCP-1-beta
Atrial fibrillation, Atrial flutter, Leber congenital amaurosis, Osteoporosis, Retinitis pigmentosa

547
Chaperonin containing TCP1 subunit 3
CCT-gamma, CCTG, NEDSVH, PIG48, TCP-1-gamma, TRIC5
Alzheimer disease, Neurodevelopmental disorder, Osteoarthritis, Parkinson disease

548
Chaperonin containing TCP1 subunit 4
CCT-DELTA, Cctd, SRB
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

549
Chaperonin containing TCP1 subunit 5
CCT-epsilon, CCTE, HEL-S-69, HSNSP, PNAS-102, TCP-1-epsilon
Breast neoplasms, Neurodevelopmental disorder, Hereditary sensory and autonomic neuropathy with spastic paraplegia, Hereditary sensory and autonomic neuropathy, Non-specific syndromic intellectual disability, Hereditary spastic paraplegia

550
Chaperonin containing TCP1 subunit 6A
CCT-zeta, CCT-zeta-1, CCT6, Cctz, HTR3, MoDP-2, TCP-1-zeta, TCP20, TCPZ, TTCP20
Neurodevelopmental disorder, Coronary artery disease, Non-specific syndromic intellectual disability