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
3281 to 3290 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3281
CYFIP related Rac1 interactor A
CYRI-A, FAM49A
Astrocytoma, Attention deficit hyperactivity disorder, Basal cell carcinoma, Central nervous system cancer, Clonal hematopoiesis, Dementia, Dry eye syndrome, Glioma, Keratinocyte carcinoma, Alzheimer disease, Liver cirrhosis, Myeloproliferative disorder, Nephrolithiasis, Non-melanoma skin carcinoma, Orofacial cleft
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3282
CYFIP related Rac1 interactor B
BM-009, CYRI, CYRI-B, FAM49B, L1
Alzheimer disease, Androgenetic alopecia, Colorectal cancer, Heart failure, Liver cirrhosis, Migraine, Parkinson disease, Post-traumatic stress disorder, Rheumatoid arthritis, Schizophrenia

3283
Cystin 1
-
Atrial fibrillation, Polycystic kidney disease, Bronchitis, Obstructive pulmonary disease, Gout

3284
Cysteinyl leukotriene receptor 1
CYSLT1, CYSLT1R, CYSLTR, HMTMF81
Asthma, Coronary artery disease, Rhinitis

3285
Cysteinyl leukotriene receptor 2
CYSLT2, CYSLT2R, GPCR21, HG57, HPN321, KPG_011, PSEC0146, hGPCR21
Asthma, Atrial fibrillation, Ovarian epithelial cancer, Ovarian cancer, Pulmonary fibrosis, Juvenile idiopathic arthritis, Uveal melanoma

3286
Cysteine rich transmembrane module containing 1
C5orf32, ORF1-FL49
Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Hypertension, Liver cirrhosis, Major depressive disorder, Post-traumatic stress disorder, Schizophrenia

3287
Mitochondrially encoded cytochrome b
MTCYB
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss

3288
-
-
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss

3289
-
-
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss

3290
Cytohesin 1
B2-1, CYTOHESIN-1, D17S811E, PSCD1, SEC7
Atrial fibrillation, Coronary artery disease, Heart failure, Major depressive disorder, Diabetes mellitus type 2, Ulcerative colitis