Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1741 to 1750 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1741
Calmodulin regulated spectrin associated protein family member 3
KIAA1543, NEZHA, PPP1R80
Female infertility, Peripheral arterial disease

1742
Calmodulin binding transcription activator 1
CANPMR, CECBA
Alzheimer disease, Attention deficit hyperactivity disorder, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Colorectal cancer, Fatty liver, Gastroesophageal reflux disease, Insomnia, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Migraine, Mood disorder, Nervous system disease, Neurodevelopmental disorder, Neurotic disorder
View all (8 more)

1743
Calmodulin binding transcription activator 2
-
Cerebellar dysfunction with variable cognitive and behavioral abnormalities

1744
Cullin associated and neddylation dissociated 1
TIP120, TIP120A
Scoliosis

1745
Cullin associated and neddylation dissociated 2 (putative)
TIP120B, Tp120b
Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardiomyopathy, Heart failure, Diabetes mellitus type 2

1746
Calcium activated nucleotidase 1
DBQD, DBQD1, EDM7, SCAN-1, SCAN1, SHAPY
Desbuquois dysplasia, Desbuquois syndrome, Epiphyseal dysplasia, Larsen syndrome

1747
Calnexin
CNX, IP90, P90
Alzheimer disease, Myocardial ischemia

1748
Cyclase associated actin cytoskeleton regulatory protein 1
CAP, CAP1-PEN
Atrial fibrillation, Osteoporosis

1749
Cyclase associated actin cytoskeleton regulatory protein 2
CMD2I
Autoimmune thrombocytopenic purpura, Hepatocellular carcinoma, Dilated cardiomyopathy, Hemorrhoid, Neuroblastoma

1750
Capping actin protein, gelsolin like
AFCP, HEL-S-66, MCP
Renal cell carcinoma, Myeloid leukemia