|
391
|
|
|
MiR-17-92a-1 cluster host gene |
C13orf25, LINC00048, MIHG1, MIRH1, MIRHG1, NCRNA00048, miR-17-92 |
Bone disease, Brachydactyly, Congenital anomaly of limb, Congenital microcephaly, Coronary heart disease, Diabetes mellitus, Dwarfism, Feingold syndrome, Hypoplasia of thumb, Mental retardation, Microcephaly, Microlissencephaly |
|
392
|
|
|
Mab-21 like 1 |
CAGR1, COFG, Nbla00126 |
Cerebellar hypoplasia, Dandy-walker syndrome, Developmental delay, Glaucoma, congenital, Horizontal nystagmus, Keratoconjunctivitis sicca, Mental retardation, Posteriorly rotated ear, Strabismus, Synophrys |
|
393
|
|
|
Myristoylated alanine rich protein kinase C substrate |
80K-L, MACS, PKCSL, PRKCSL |
|
|
394
|
|
|
MAX dimerization protein 1 |
BHLHC58, MAD, MAD1 |
|
|
395
|
|
|
Mitotic arrest deficient 2 like 1 |
HSMAD2, MAD2 |
|
|
396
|
|
|
MAF bZIP transcription factor |
AYGRP, CCA4, CTRCT21, c-MAF |
Ayme-gripp syndrome, Brachycephaly, Brachydactyly, Cataract, Pulverulent cataract, Cataract-microcornea syndrome, Colorectal cancer, Colorectal neoplasms, Congenital cataract, Congenital coloboma of iris, Corneal dystrophy, Cortical cataract, Dwarfism, Hearing loss, Intrahepatic cholestasis, Mental retardation, Microcornea, Microstomia, Myopia, Nystagmus, Ptosis, Radioulnar synostosisView all (7 more) |
|
397
|
|
|
MAF bZIP transcription factor G |
hMAF |
|
|
398
|
|
|
Myelin associated glycoprotein |
GMA, S-MAG, SIGLEC-4A, SIGLEC4, SIGLEC4A, SPG75 |
Astigmatism, Atrophy of corpus callosum, Cerebellar atrophy, Developmental delay, Distal lower limb amyotrophy, Hyperopia, Impaired cognition, Lewy body disease, Mental retardation, Hypotonia, Nervous system diseases, Nystagmus, Optic atrophy, Parkinson disease, Schizophrenia, Spastic paraplegia, Temporal pallor of optic discView all (2 more) |
|
399
|
|
|
MAGE family member A1 |
CT1.1, MAGE1 |
|
|
400
|
|
|
MAGE family member A3 |
CT1.3, HIP8, HYPD, MAGE3, MAGEA6 |
|
