Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2961 to 2970 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2961
Cellular retinoic acid binding protein 2
CRABP-II, RBP6
Aortic disease, Methylmalonic acidemia, Neutropenia, Ovarian neoplasms

2962
Capping protein inhibiting regulator of actin dynamics
CRAD, KIAA1211
Coronary artery disease, Lung cancer, Obesity, Scoliosis, Squamous cell carcinoma

2963
CRACD like
C2orf55, KIAA1211L
Bipolar disorder

2964
Calcium release activated channel regulator 2A
EFCAB4B, RAB46
Liver cirrhosis, Combined immunodeficiency disease, Male infertility, Nonalcoholic fatty liver disease, Periodontitis, Sialolithiasis

2965
Calcium release activated channel regulator 2B
EFCAB4A
Bronchitis, Obstructive pulmonary disease, Obesity

2966
CARD and death domain containing adaptor protein
MRT34, RAIDD
Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Nonsyndromic intellectual disability, Bone fracture, Renal cell carcinoma, Dementia, Arrhythmogenic right ventricular dysplasia, Global developmental delay, Hypertension, Intellectual developmental disorder, Osteoarthritis, Scoliosis, Diabetes mellitus type 2

2967
Cramped chromatin regulator 1
CRAMP1L, HN1L, TCE4
Atrial fibrillation, Epilepsy, Prostate cancer

2968
Carnitine O-acetyltransferase
CAT, CAT1, NBIA8
Eczema, Carnitine acetyltransferase deficiency, Neurodegeneration with brain iron accumulation, Pelvic organ prolapse

2969
Crumbs cell polarity complex component 1
CRB1-A, CRB1-B, CRB1-C, LCA8, RP12
Leber congenital amaurosis, Ankylosing spondylitis, Anorexia nervosa, Asthma, Autoimmune disease, Autoimmune thyroid disease, Retinitis pigmentosa, Bestrophinopathy, Celiac disease, Color vision deficiency, Common variable immunodeficiency, Cone dystrophy, Cone-rod dystrophy, Crohn disease, Eating disorder
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2970
Crumbs cell polarity complex component 2
FSGS9, VMCKD
Astrocytoma, Central nervous system cancer, Cystic kidney disease with ventriculomegaly, Dementia, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glioblastoma, Glioma, Hereditary steroid-resistant nephrotic syndrome, Metabolic syndrome, Nephrotic syndrome, focal segmental type, Oligodendroglioma, Retinitis pigmentosa
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