Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7611 to 7620 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7611
MARCKS like 1
F52, MACMARCKS, MLP, MLP1, MRP
Basal cell carcinoma

7612
Macrophage receptor with collagenous structure
SCARA2, SR-A6
Hepatocellular carcinoma

7613
Microtubule affinity regulating kinase 1
MARK, Par-1c, Par1c
Autism, Stomach neoplasms

7614
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

7615
Microtubule affinity regulating kinase 3
CTAK1, KP78, PAR1A, Par-1a, VIPB
Cardiovascular disease, Color vision deficiency, Coronary artery disease, Melanoma, Eye disorder, Endometriosis, Gout, Hypertension, Insomnia, Major depressive disorder, Metabolic syndrome, Osteoarthritis, Otosclerosis, Pancreatic cancer, Squamous cell carcinoma
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7616
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

7617
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

7618
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

7619
MARVEL domain containing 1
GB14, MARVD1, MRVLDC1, bA548K23.8
Alzheimer disease

7620
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