Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2951 to 2960 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2951
Calcium release activated channel regulator 2A
EFCAB4B, RAB46
Liver cirrhosis, Combined immunodeficiency disease, Male infertility, Nonalcoholic fatty liver disease, Periodontitis, Sialolithiasis

2952
Calcium release activated channel regulator 2B
EFCAB4A
Bronchitis, Obstructive pulmonary disease, Obesity

2953
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

2954
Cramped chromatin regulator 1
CRAMP1L, HN1L, TCE4
Atrial fibrillation, Epilepsy, Prostate cancer

2955
Carnitine O-acetyltransferase
CAT, CAT1, NBIA8
Eczema, Carnitine acetyltransferase deficiency, Neurodegeneration with brain iron accumulation, Pelvic organ prolapse

2956
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
View all (19 more)

2957
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
View all (4 more)

2958
Cereblon
MRT2, MRT2A
Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Bipolar disorder, Cholecystitis, Cholecystolithiasis, Congenital neurologic anomalies, Eating disorder, Intellectual developmental disorder, Multiple myeloma, Osteoarthritis, Pancreatic cancer, Willis-ekbom disease, Scoliosis
View all (4 more)

2959
CGRP receptor component
C17, CGRP-RCP, CGRPRCP, POLR3I, POLR3J, RCP, RCP9, RPC9
Diabetic neuropathy, Psychiatric disorders

2960
Cysteine rich C-terminal 1
C1orf42, NICE-1, NICE1
Asthma, Eczema, Inflammatory skin disease, Obesity, Psoriasis