|
401
|
|
|
MAGE family member A4 |
CT1.4, MAGE-41, MAGE-X2, MAGE4, MAGE4A, MAGE4B |
|
|
402
|
|
|
MAGE family member A6 |
CT1.6, MAGE-3b, MAGE3B, MAGE6 |
|
|
403
|
|
|
MAGE family member A9 |
CT1.9, MAGE9 |
|
|
404
|
|
|
Male germ cell associated kinase |
RP62 |
Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Infiltrating duct carcinoma of female breast, Keratoconus, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (2 more) |
|
405
|
|
|
Mal, T cell differentiation protein (MAL blood group) |
HLD28, MVP17, VIP17 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Head and neck cancer, Marfan syndrome, Neck neoplasms, Upper aerodigestive tract neoplasms |
|
406
|
|
|
Mannosidase alpha class 2A member 2 |
MANA2X, alpha-MIIx |
|
|
407
|
|
|
Mannosidase alpha class 2C member 1 |
CDDG2, MAN6A8, MANA, MANA1 |
|
|
408
|
|
|
Mannosidase alpha class 2A member 1 |
AMan II, GOLIM7, MANA2, MANII |
|
|
409
|
|
|
Mannosidase alpha class 2B member 1 |
LAMAN, MANB |
Alpha-mannosidosis, Cerebellar atrophy, Cerebral atrophy, Congenital epicanthus, Congenital pectus carinatum, Developmental delay, Dysarthria, Dysmorphic features, Frontal bossing, Glomerulonephritis, Hearing loss, Hypertrichosis, Macrocephaly, Macroglossia, Macrotia, Malocclusion, Mental retardation, Movement disorders, Multiple congenital anomalies, Nystagmus, Pfaundler-hurler syndrome, Spinocerebellar tract disease in lower limbs, SpondylolisthesisView all (8 more) |
|
410
|
|
|
Mannosidase beta |
MANB1 |
Angiokeratoma, Asthma, Attention deficit hyperactivity disorder, Beta-mannosidosis, Cholangitis, Lysosomal beta-mannosidase deficiency, Mental retardation, Multiple sclerosis, Biliary cirrhosis, Sarcoidosis, Speech disorders |
