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
1761 to 1770 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1761
Calpain 8
nCL-2
Astrocytoma, Celiac disease, Color vision deficiency, Endometrial cancer

1762
Calpain 9
GC36, nCL-4
Colorectal cancer

1763
Calpain small subunit 1
CALPAIN4, CANP, CANPS, CAPN4, CDPS, CSS1, PPH6
Prostatic neoplasms, Pulmonary hypertension

1764
Cell cycle associated protein 1
CONDCAC, GPIAP1, GPIP137, GRIP137, M11S1, NEDLAAD, RNG105, p137GPI
Autism, Cerebellar ataxia, Developmental and epileptic encephalopathy, Myoclonic epilepsy, Major depressive disorder, Moyamoya angiopathy, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Post-operative acute kidney injury, Seizures

1765
Caprin family member 2
C1QDC1, EEG-1, EEG1, RNG140
Cataract, Colorectal cancer, Exostoses

1766
Calcyphosine 2
UG0636c06
Intellectual developmental disorder

1767
Calcyphosine like
-
Ankylosing spondylitis, Asthma, Eczema, Autism, B-cell acute lymphoblastic leukemia, Biliary cirrhosis, Dermatitis, Biliary cholangitis, Respiratory system disease, Rhinitis, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2

1768
Capping actin protein of muscle Z-line subunit alpha 1
CAPPA1, CAPZ, CAZ1
Esophageal squamous cell carcinoma, Hypertension, Major depressive disorder

1769
Capping actin protein of muscle Z-line subunit alpha 2
CAPPA2, CAPZ
Alzheimer disease, Neurodevelopmental disorder, Insomnia, Intellectual developmental disorder, Non-specific syndromic intellectual disability

1770
Capping actin protein of muscle Z-line subunit alpha 3
CAPPA3, Gsg3, HEL-S-86
Alzheimer disease, Attention deficit hyperactivity disorder, Chagas cardiomyopathy, Obstructive pulmonary disease, Gastroesophageal reflux disease, Psychiatric disorders, Substance abuse