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
2031 to 2040 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2031
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
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2032
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

2033
Chaperonin containing TCP1 subunit 3
CCT-gamma, CCTG, NEDSVH, PIG48, TCP-1-gamma, TRIC5
Alzheimer disease, Neurodevelopmental disorder, Osteoarthritis, Parkinson disease

2034
Chaperonin containing TCP1 subunit 4
CCT-DELTA, Cctd, SRB
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

2035
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

2036
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

2037
Chaperonin containing TCP1 subunit 6B
CCT-zeta-2, CCTZ-2, Cctz2, TCP-1-zeta-2, TSA303
Brain cancer, Brain neoplasms, Burkitt lymphoma, Glioma, Glomerulonephritis, Insomnia, Amyotrophic lateral sclerosis

2038
Chaperonin containing TCP1 subunit 7
CCTETA, CCTH, NIP7-1, TCP1ETA
Neurodevelopmental disorder, Kidney failure, Non-specific syndromic intellectual disability, Stomach neoplasms

2039
Chaperonin containing TCP1 subunit 8
C21orf112, Cctq, D21S246, PRED71
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

2040
CCZ1 vacuolar protein trafficking and biogenesis associated
C7orf28A, CCZ1A, CGI-43, H_DJ1163J12.2
Dementia