Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
691 to 700 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

691
Complement factor H related 1
CFHL, CFHL1, CFHL1P, CFHR1P, FHL-1, FHR-1, FHR1, H36, H36-1, H36-2, HFL1, HFL2
C3 glomerulonephritis, C3 glomerulopathy, Complement component deficiency, Dense deposit disease, Dysphasia, Geographic atrophy, Glomerulonephritis, Hemolytic uremic syndrome, Hyperlipidemia, Hypertension, Impaired cognition, Age-related macular degeneration, Microangiopathic hemolytic anemia, Nephrotic syndrome

692
Complement factor H related 2
CFHL2, FHR2, HFL3
C3 glomerulopathy, Complement component deficiency, Age-related macular degeneration

693
Chromosome 14 open reading frame 39
POF18, SPGF52, Six6os1
Glaucoma, Optic disc anomalies with retinal and/or macular dystrophy

694
C-type lectin domain family 4 member D
CD368, CLEC-6, CLEC6, CLECSF8, Dectin-3, MCL, MPCL
Lung diseases

695
CBY1 interacting BAR domain containing 2
FAM92B
Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Ileocolitis

696
Chromosome 17 open reading frame 67
-
Ankylosing spondylitis, Cholangitis, Crohn disease, Hemolytic uremic syndrome, Inflammatory bowel disease, Nephrotic syndrome, Psoriasis, Ulcerative colitis

697
Coiled-coil domain containing 137
RaRF
Schizophrenia

698
C-type lectin domain family 4 member G
DTTR431, LP2698, LSECtin, UNQ431
Liver carcinoma

699
Coiled-coil domain 39 molecular ruler complex subunit
CFAP59, CILD14, FAP59
Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Ciliopathies, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Leukemia, Lung diseases, Nasal polyposis, Otitis media
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700
Collagen type XXVIII alpha 1 chain
COL28
Frontotemporal dementia