Genes | GeDiPNet - Gene Disease Pathway & Associations

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2191 to 2200 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2191	145270	PRIMA1	Proline rich membrane anchor 1	PRIMA	Colorectal cancer, Mental depression, Muscular dystrophy
2192	145282	MIPOL1	Mirror-image polydactyly 1	CCDC193	Polydactyly
2193	1453	CSNK1D	Casein kinase 1 delta	ASPS, CKI-delta, CKId, CKIdelta, FASPS2, HCKID	Advanced sleep phase syndrome, Breast cancer, Common migraine, Migraine, Migraine with aura, Sleep phase syndrome
2194	1454	CSNK1E	Casein kinase 1 epsilon	CKIe, CKIepsilon, HCKIE	Bipolar disorder, Epileptic encephalopathy, Lung adenocarcinoma, Schizophrenia
2195	145407	ARMH4	Armadillo like helical domain containing 4	C14orf37, UT2, c14_5376	Proteasome-associated autoinflammatory syndrome, digenic
2196	145447	ABHD12B	Abhydrolase domain containing 12B	BEM46L3, C14orf29, c14_5314	Breast cancer
2197	145508	CEP128	Centrosomal protein 128	C14orf145, C14orf61, LEDP/132	Epilepsy, Graves disease, Congenital hypothyroidism, nongoitrous, Nasopharyngeal neoplasms
2198	145567	TTC7B	Tetratricopeptide repeat domain 7B	TTC7L1, c14_5685	Malignant melanoma of skin, Melanoma
2199	145581	LRFN5	Leucine rich repeat and fibronectin type III domain containing 5	C14orf146, FIGLER8, SALM5	Mental depression, Myopia
2200	145624	PWAR1	Prader Willi/Angelman region RNA 1	D15S227E, PAR-1, PAR1	Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis View all (7 more)

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