Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2151 to 2160 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2151
CDC42 binding protein kinase beta
CHOCNS, MRCKB
Autism, Neurodevelopmental disorder, Diffuse large b-cell lymphoma, Imerslund-grasbeck syndrome, Major depressive disorder, Megaloblastic anemia, Non-specific syndromic intellectual disability, Parkinson disease

2152
CDC42 binding protein kinase gamma
DMPK2, HSMDPKIN, KAPPA-200, MRCKG, MRCKgamma
Gout, Moyamoya disease, Post-traumatic stress disorder, Hypertension

2153
CDC42 effector protein 1
BORG5, CEP1, MSE55
Autoimmune hepatitis, Sarcoidosis

2154
CDC42 effector protein 2
BORG1, CEP2
Hyperuricemia

2155
CDC42 effector protein 3
BORG2, CEP3, UB1
Alzheimer disease, Prostate cancer, Rheumatoid arthritis, Schizophrenia

2156
CDC42 effector protein 5
Borg3, CEP5
Colorectal cancer

2157
CDC42 small effector 1
SCIP1, SPEC1
Liver cirrhosis, Metabolic syndrome, Osteoporosis, Diabetes mellitus type 2

2158
CDC42 small effector 2
SPEC2
Alzheimer disease, Eczema, Crohn disease, Inflammatory bowel disease, Nasal polyp, Schizophrenia, Scoliosis, Ulcerative colitis

2159
Cell division cycle 45
CDC45L, CDC45L2, MGORS7, PORC-PI-1
Androgen insensitivity syndrome, Hepatocellular carcinoma, Dementia, Desbuquois syndrome, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Meier-gorlin syndrome

2160
Cell division cycle 5 like
CDC5, CDC5-LIKE, CEF1, PCDC5RP, dJ319D22.1
Alzheimer disease, Androgenetic alopecia, Asthma, Bell's palsy, Bone disease, Congenital anomalies of the kidney and urinary tract, Diffuse idiopathic skeletal hyperostosis, Essential tremor, Facial nerve disorder, Glaucoma, Large artery stroke, Migraine, Nervous system disease, Obesity, Osteoarthritis
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