Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2611 to 2620 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2611
Claudin 4
CPE-R, CPER, CPETR, CPETR1, WBSCR8, hCPE-R
Breast neoplasms, Ductal carcinoma of breast, Mesothelioma, Polycystic ovary syndrome

2612
Claudin 5
AWAL, BEC1, CPETRL1, TMDVCF, TMVCF
Major depressive disorder, Mesothelioma, Neurodevelopmental disorder, Schizophrenia

2613
Claudin 7
CEPTRL2, CLDN-7, CPETRL2, Hs.84359, claudin-1
Rhinitis, Epithelial ovarian carcinoma, Cholecystolithiasis, Gallstones, Prostatic neoplasms

2614
Claudin 8
HEL-S-79
Gout, Mesothelioma

2615
Claudin 9
DFNB116
Deafness, Hearing impairment, Hearing loss, Pendred syndrome, Prostatic neoplasms

2616
C-type lectin domain containing 10A
CD301, CLECSF13, CLECSF14, DC-ASGPR, HML, HML2, MGL
Bipolar disorder, Congenital heart disease, Crohn disease, Diabetes mellitus, Diabetic ketoacidosis, Inflammatory bowel disease, Myocardial ischemia, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

2617
C-type lectin domain containing 11A
CLECSF3, LSLCL, P47, SCGF
Anemia, Carotid artery stenosis, Mesothelioma, Osteoporosis

2618
C-type lectin domain family 12 member A
CD371, CLL-1, CLL1, DCAL-2, MICL, hKLRL1
Rheumatoid arthritis

2619
C-type lectin domain containing 14A
C14orf27, CEG1, EGFR-5
Central nervous system cancer, Color vision deficiency, Coronary vasospasm, Diabetes mellitus, Glioblastoma, Glioma, Diabetes mellitus type 2

2620
C-type lectin domain containing 16A
Gop-1, KIAA0350
Ankylosing spondylitis, Asthma, Eczema, Basal cell carcinoma, Biliary cirrhosis, Rhinosinusitis, Common variable immunodeficiency, Crohn disease, Dermatitis, Diabetes mellitus type 1, Diverticular disease, Eosinophilia, Hodgkin lymphoma, Selective immunoglobulin a deficiency, Liver cirrhosis
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