Genes | GeDiPNet - Gene Disease Pathway & Associations

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7891 to 7900 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
7891	4288	MKI67	Marker of proliferation Ki-67	KIA, MIB-, MIB-1, PPP1R105	Breast neoplasms, Hepatocellular carcinoma, Chondrosarcoma, Colonic neoplasms, Colorectal neoplasms, Copper overload cirrhosis, Crohn disease, Graft-versus-host disease, Liver cirrhosis, Non-neoplastic peripheral nervous system disease, Ovarian neoplasms, Peripheral nervous system disease, Peripheral neuropathy, Psoriasis
7892	8195	MKKS	MKKS centrosomal shuttling protein	BBS6, HMCS, KMS, MKS	Alzheimer disease, Bardet-biedl syndrome, Congenital heart defects, Nephronophthisis, Obesity, Polycystic kidney disease, Cone dystrophy, Retinitis pigmentosa
7893	4289	MKLN1	Muskelin 1	TWA2	Alzheimer disease, Androgenetic alopecia, Asthma, Bipolar disorder, Central nervous system cancer, Melanoma, Dementia, Glioblastoma, Glioma, Lung cancer, Major depressive disorder, Pulmonary fibrosis, Schizophrenia, Urinary system disease
7894	8569	MKNK1	MAPK interacting serine/threonine kinase 1	MNK1	Kidney disease, Hypertension, Schizophrenia
7895	2872	MKNK2	MAPK interacting serine/threonine kinase 2	GPRK7, MNK2	Carpal tunnel syndrome
7896	23608	MKRN1	Makorin ring finger protein 1	RNF61	Alzheimer disease, Endometriosis
7897	23609	MKRN2	Makorin ring finger protein 2	HSPC070, RNF62	Gout, Leopard syndrome, Noonan syndrome
7898	100129480	MKRN2OS	MKRN2 opposite strand	C3orf83, MKRN2-AS1	Hypertrophic cardiomyopathy, Systemic lupus erythematosus
7899	7681	MKRN3	Makorin ring finger protein 3	CPPB2, D15S9, RNF63, ZFP127, ZNF127	Central precocious puberty, Prader-willi syndrome, Scoliosis
7900	54903	MKS1	MKS transition zone complex subunit 1	BBS13, JBTS28, MES, MKS, POC12	Bardet-biedl syndrome, Kidney disease, Ciliopathy, Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Global developmental delay, Joubert syndrome, Leber congenital amaurosis, Meckel-gruber syndrome, Nystagmus, Optic atrophy, Peripheral neuropathy, Polycystic kidney disease, Polydactyly View all (3 more)

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