Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1731 to 1740 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1731
Calcium/calmodulin dependent protein kinase II inhibitor 1
PRO1489
Alzheimer disease, Periodontal disease, Periodontitis

1732
Calcium/calmodulin dependent protein kinase IV
CaMK IV, CaMK-GR, CaMKIV, caMK
Alzheimer disease, Asthma, Autoimmune disease, Autoimmune thyroid disease, Colorectal cancer, Neurodevelopmental disorder, Hypothyroidism, Insomnia, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Periodontitis, Severe combined immunodeficiency, Diabetes mellitus type 1, Diabetes mellitus type 2

1733
Calcium/calmodulin dependent protein kinase kinase 1
CAMKKA
Systemic scleroderma, Central nervous system cancer, Glioblastoma, Glioma, Nervous system disease

1734
Calcium/calmodulin dependent protein kinase kinase 2
CAMKK, CAMKKB
Anorexia nervosa, Coronary artery disease, Major depressive disorder, Obesity, Obsessive-compulsive disorder, Ovarian neoplasms, Prostatic neoplasms, Schizophrenia, Diabetes mellitus type 2

1735
Calmodulin-lysine N-methyltransferase
C2orf34, CLNMT, CaM KMT, Cam, KMT
Hypotonia-cystinuria syndrome, Bipolar disorder, Cannabis abuse, Cholecystolithiasis, Developmental coordination disorder, Developmental disability, Essential tremor, Learning disorders, Major depressive disorder, Metabolic syndrome, Mitochondrial myopathy, Motor skills disorder, Obstructive sleep apnea syndrome, Ovarian cancer, Ovarian serous carcinoma
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1736
CaM kinase like vesicle associated
1G5, VACAMKL
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Inflammatory bowel disease, Osteoarthritis, Post-traumatic stress disorder

1737
Calcium modulating ligand
CAML, CDG2Z, GET2
Congenital disorder of glycosylation

1738
Cathelicidin antimicrobial peptide
CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26, LL37
Rosacea

1739
Calmodulin regulated spectrin associated protein 1
CDCBM12
Alzheimer disease, Juvenile arthritis, Colorectal cancer, Cortical dysplasia with other brain malformations, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Scoliosis

1740
Calmodulin regulated spectrin associated protein family member 2
CAMSAP1L1
Celiac disease, Epilepsy, Generalized epilepsy, Hypothyroidism, Myocardial infarction, Partial epilepsy, Diabetes mellitus type 1, Diabetes mellitus type 2, Venous thromboembolism