Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

161 to 170 of 898 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
161	8685	MARCO	Macrophage receptor with collagenous structure	SCARA2, SR-A6	Hepatocellular carcinoma, Intestinal infectious disease
162	4139	MARK1	Microtubule affinity regulating kinase 1	MARK, Par-1c, Par1c	Autism, Stomach neoplasms
163	2011	MARK2	Microtubule affinity regulating kinase 2	EMK-1, EMK1, MRD76, PAR-1, Par-1b, Par1b	Alzheimer disease, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Adenoid cystic carcinoma, Dyslexia, Hyperuricemia, Intellectual developmental disorder, Major depressive disorder, Obsessive-compulsive disorder, Salivary gland neoplasms, Schizophrenia
164	4140	MARK3	Microtubule affinity regulating kinase 3	CTAK1, KP78, PAR1A, Par-1a, VIPB	Cardiovascular disease, Color vision deficiency, Coronary artery disease, Melanoma, Disorder of eye, Endometriosis, Gout, Hypertension, Insomnia, Major depressive disorder, Metabolic syndrome, Osteoarthritis, Otosclerosis, Pancreatic cancer, Squamous cell carcinoma View all (2 more)
165	57787	MARK4	Microtubule affinity regulating kinase 4	MARK4L, MARK4S, MARKL1, MARKL1L, PAR-1D	Alzheimer disease, Atrophic macular degeneration, Coronary artery disease, Gastroesophageal reflux disease, Hyperopia, Metabolic syndrome, Myocardial infarction, Neurodevelopmental disorder, Peptic ulcer disease, Scoliosis, Diabetes mellitus type 2, Age-related macular degeneration
166	4141	MARS1	Methionyl-tRNA synthetase 1	CMT2U, ILFS2, ILLD, MARS, METRS, MRS, MTRNS, SPG70, TTD9	Charcot-marie-tooth disease, Spastic paraplegia, Dejerine-sottas disease, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Interstitial lung disease, Peroneal muscle atrophy, Roussy-levy syndrome, Hereditary spastic paraplegia, Trichothiodystrophy, Diabetes mellitus type 1, Diabetes mellitus type 2
167	92935	MARS2	Methionyl-tRNA synthetase 2, mitochondrial	COXPD25, MetRS, mtMetRS	Ataxia, spastic, autosomal recessive, Spastic ataxia with leukoencephalopathy, Combined oxidative phosphorylation deficiency, Dilated cardiomyopathy, Mitochondrial disease, Rheumatoid arthritis, Spastic ataxia, Stroke, Systemic lupus erythematosus
168	83742	MARVELD1	MARVEL domain containing 1	GB14, MARVD1, MRVLDC1, bA548K23.8	Alzheimer disease
169	153562	MARVELD2	MARVEL domain containing 2	DFNB49, MARVD2, MRVLDC2, Tric	Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss
170	91862	MARVELD3	MARVEL domain containing 3	MARVD3, MRVLDC3	Gout, Diabetes mellitus type 2

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