|
101
|
|
|
Microspherule protein 1 |
ICP22BP, INO80Q, MCRS2, MSP58, P78 |
|
|
102
|
|
|
Mitotic arrest deficient 2 like 2 |
FANCV, MAD2B, POLZ2, REV7 |
Anemia, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Neutropenia, Nystagmus, Patent ductus arteriosus, Proptosis, Ptosis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallotView all (33 more) |
|
103
|
|
|
MER proto-oncogene, tyrosine kinase |
MER, RP38, Tyro12, c-Eyk, c-mer |
Anaplastic carcinoma, Anetoderma, Carcinoma, Carcinoma of the head and neck, Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Glomerulonephritis, Hearing loss, Hereditary paraganglioma-pheochromocytoma syndromes, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Leukemia, Liver cirrhosis, Mental retardation, Multiple sclerosis, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Peripheral retinal atrophy, Pulmonary thromboembolism, Renal carcinoma, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (15 more) |
|
104
|
|
|
MYB binding protein 1a |
P160, PAP2, Pol5 |
|
|
105
|
|
|
MRAP antisense RNA 1 |
- |
|
|
106
|
|
|
Myocardin-induced smooth muscle lncRNA, inducer of differentiation |
- |
|
|
107
|
|
|
MECOM antisense RNA 1 |
- |
|
|
108
|
|
|
MNX1 antisense RNA 2 |
- |
|
|
109
|
|
|
MPPED2 antisense RNA 1 |
- |
|
|
110
|
|
|
MIR3659 host gene |
- |
|
