Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
891 to 900 of 971 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

891
Melanin concentrating hormone receptor 2
GPR145, GPRv17, MCH-2R, MCH-R2, MCH2, MCH2R, MCHR-2, SLT
Bipolar disorder, Schizophrenia

892
MAK16 homolog
MAK16L, RBM13
Mental retardation

893
Metallothionein 4
MT-4, MT-IV, MTIV
Kidney disease

894
Myopalladin
CMD1DD, CMH22, CMYO24, CMYP24, MYOP, NEM11, RCM4
Amyotrophy, Arthrogryposis multiplex congenita, Atrial fibrillation, Cap myopathy, Cardiomyopathy, Cholecystolithiasis, Cholelithiasis, Congenital pectus excavatum, Dilated cardiomyopathy, Facial paralysis, Hearing loss, High palate, Hypertrophic cardiomyopathy, Limb muscle atrophy, Lipoatrophy
View all (15 more)

895
Membrane spanning 4-domains A14
MS4A16, NYD-SP21
Leukemia

896
Methylmalonyl-CoA epimerase
GLOD2, MCE, MMCE
Gastroesophageal reflux disease, Ketonuria, Methylmalonic aciduria, Methylmalonyl-coa epimerase deficiency

897
Myosin XVIIIB
KFS4
Atrial fibrillation, Cardiomyopathy, Developmental dysplasia of the hip, High palate, Klippel-feil anomaly-myopathy-facial dysmorphism syndrome, Klippel feil syndrome, Klippel-feil syndrome with nemaline myopathy and facial dysmorphism, Leukemia, Lung carcinoma, Lung adenocarcinoma, Mesothelioma, Microcephaly, Micrognathism, Myopathy, Neck webbing
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898
Mitochondria localized glutamic acid rich protein
C4orf49, CESP-1, HUMMR, OSAP
Rheumatoid arthritis

899
MPV17 mitochondrial inner membrane protein like 2
FKSG24
Multiple sclerosis

900
MFSD2 lysolipid transporter A, lysophospholipid
HsMFSD2A, MCPH15, MFSD2, NEDMISBA, NLS1, SLC59A1
Agenesis of corpus callosum, Cerebellar hypoplasia, Congenital clubfoot, Congenital microcephaly, Developmental delay, Dwarfism, Dyslalia, Hypoplasia of corpus callosum, Mental retardation, Liver carcinoma, Microcephaly, Microlissencephaly, Neuronal heterotopia, Pachygyria, Renal aplasia
View all (3 more)