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 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1761
Calpain 14
-
Amyotrophic lateral sclerosis, Breast disease, Endometriosis, Eosinophilia, Diabetes mellitus type 2

1762
Calpain 15
OGIN, SOLH
Congenital heart disease, Congenital ocular coloboma

1763
Calpain 2
CANP2, CANPL2, CANPml, mCANP
Central nervous system cancer, Cognition disorder, Delirium, dementia, and cognitive disorders, Glioblastoma, Glioma, Hypoplastic left heart syndrome, Myeloid leukemia, Schizophrenia

1764
Calpain 3
CANP3, CANPL3, LGMD2, LGMD2A, LGMDD4, LGMDR1, nCL-1, p94
Limb girdle muscular dystrophy, Cardiac arrhythmia, Congenital muscular dystrophy, Limb-girdle muscular dystrophy, Metabolic syndrome, Migraine, Muscular dystrophy, Myopathy, Paresthesia, Diabetes mellitus type 2

1765
Calpain 5
ADNIV, HTRA3, VRNI, nCL-3
Neovascular inflammatory vitreoretinopathy, Vitreoretinopathy, Eosinophilia, Retinitis pigmentosa

1766
Calpain 8
nCL-2
Astrocytoma, Celiac disease, Color vision deficiency, Endometrial cancer

1767
Calpain 9
GC36, nCL-4
Colorectal cancer

1768
Calpain small subunit 1
CALPAIN4, CANP, CANPS, CAPN4, CDPS, CSS1, PPH6
Prostatic neoplasms, Pulmonary hypertension

1769
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

1770
Caprin family member 2
C1QDC1, EEG-1, EEG1, RNG140
Cataract, Colorectal cancer, Exostoses