Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "M"
361 to 370 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
Mitofusin 1
hfzo1, hfzo2
Amyotrophic lateral sclerosis, Breast cancer, Neuronal ceroid lipofuscinosis, Gout, Scoliosis

362
Mitofusin 2
CMT2A, CMT2A2, CMT2A2A, CMT2A2B, CPRP1, HMSN6A, HSG, MARF, MSL
Amyotrophic lateral sclerosis, Autoimmune neurological syndrome, Eczema, Auditory neuropathy, Charcot-marie-tooth disease, Axonal hereditary motor and sensory neuropathy, Cardiomegaly, Cerebellar ataxia, Cerebral palsy, Dejerine-sottas disease, Diabetic neuropathy, Nail dystrophy, Global developmental delay, Hereditary motor and sensory neuropathies, Motor neuron disease
View all (12 more)

363
Membrane frizzled-related protein
CTRP5, MCOP5, NNO2, RD6
Gout, Microphthalmia, Microphthalmia with retinitis pigmentosa and ocular anomalies, Microphthalmos, Nanophthalmos, Optic atrophy, Retinitis pigmentosa

364
Major facilitator superfamily domain containing 1
Minerva, SLC72A1, SMAP4
Obstructive pulmonary disease, Insomnia, Periodontitis

365
Major facilitator superfamily domain containing 12
C19orf28, PP3501, SLC59B1
Crohn disease, Melanoma, Inflammatory bowel disease

366
MFSD2 lysolipid transporter A, lysophospholipid
HsMFSD2A, MCPH15, MFSD2, NEDMISBA, NLS1, SLC59A1
Primary microcephaly, Hepatocellular carcinoma, Cryptorchidism, Febrile convulsion, Gross motor development delay, Intellectual developmental disorder, Metabolic syndrome, Microcephaly, Neurodevelopmental disorder, Diabetes mellitus type 2

367
MFSD2 lysolipid transporter B, sphingolipid
SLC59A2
Alzheimer disease

368
Major facilitator superfamily domain containing 6
MMR2, SLC73A1, hMMR2
Autoimmune disease, Color vision deficiency, Juvenile idiopathic arthritis, Systemic lupus erythematosus

369
Major facilitator superfamily domain containing 6 like
SLC73A2
Attention deficit hyperactivity disorder, Cataract, Squamous cell carcinoma

370
Major facilitator superfamily domain containing 8
CCMD, CLN7, SLC74A1
Neuronal ceroid lipofuscinosis, Cone-rod dystrophy, Congenital neurologic anomalies, Macular dystrophy, Microcephaly, Optic atrophy, Retinitis pigmentosa, Stargardt disease