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"
301 to 310 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

301
MEFV innate immunity regulator, pyrin
FMF, MEF, PAAND, TRIM20
Ankylosing spondylitis, Psoriatic arthritis, Asthma, Autoinflammatory syndrome, Behcet disease, Congenital heart defects, Henoch schoenlein purpura, Intermittent hydrarthrosis, Lung disease, Systemic lupus erythematosus, Neuronal ceroid lipofuscinosis, Peripheral neuropathy, Sweet syndrome, Urticaria

302
Multiple EGF like domains 10
CMYO10A, CMYO10B, CMYP10A, CMYP10B, EMARDD, SR-F3
Alzheimer disease, Congenital myopathy, Deglutition disorder, Early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome, Hearing loss, Myopathy, Psoriasis, Psychiatric disorders, Colorectal cancer, Schizophrenia

303
Multiple EGF like domains 11
-
Gastric cancer, Hodgkin lymphoma, Insomnia, Lymphoid leukemia, Major depressive disorder, Oligodendroglioma

304
Multiple EGF like domains 6
EGFL3
Bladder exstrophy, Breast cancer, Obstructive pulmonary disease, Systemic mastocytosis

305
Multiple EGF like domains 8
C19orf49, CRPT2, EGFL4, SBP1
Carpenter syndrome, Color vision deficiency, Craniosynostosis, Desbuquois syndrome, Polydactyly

306
Multiple EGF like domains 9
EGFL5
Central serous retinopathy, Lung cancer, Squamous cell carcinoma

307
Meiotic double-stranded break formation protein 1
HYDM3, SPATA38
Alzheimer disease, Atrial fibrillation, Hydatidiform mole, Major depressive disorder

308
Meiotic double-stranded break formation protein 4
-
Alzheimer disease, Eczema, Atrial fibrillation, Benign prostatic hyperplasia, Breast cancer, Cardiovascular disease, Cervical polyp, Color vision deficiency, Coronary artery disease, Female infertility, Heart failure, Hypertension, Metabolic syndrome, Nonalcoholic fatty liver disease, Scoliosis
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309
Meiotic kinetochore factor
SPO13
Alzheimer disease, Breast cancer

310
Meiosis specific with OB-fold
C16orf73, POF23, SPGF22, gs129
Azoospermia, Male infertility single gene azoospermia, Premature ovarian failure, Spermatogenic failure