121
|
|
|
MALT1 paracaspase |
IMD12, MLT, MLT1, PCASP1 |
Anemia, B-cell lymphoma, Diffuse lymphoma, Immunodeficiency, Immunologic deficiency syndromes, Malt lymphoma, Mediastinal lymphadenopathy, Mucosa-associated lymphoma, Multiple sclerosis, Severe combined immunodeficiency disease, Uveitis |
122
|
|
|
Myotubularin related protein 11 |
CRA |
|
123
|
|
|
MAGE family member D2 |
11B6, BARTS5, BCG-1, BCG1, HCA10, MAGE-D2 |
|
124
|
|
|
Mortality factor 4 like 1 |
Eaf3, FWP006, HsT17725, MEAF3, MORFRG15, MRG15, S863-6 |
|
125
|
|
|
MSL complex subunit 3 |
MRSXBA, MRXS36, MRXSBA, MSL3L1 |
|
126
|
|
|
Microtubule associated protein RP/EB family member 2 |
CSCSC2, EB1, EB2, RP1 |
Congenital epicanthus, Congenital exomphalos, Congestive heart failure, Cryptorchidism, Developmental delay, Dwarfism, Hypoplasia of corpus callosum, Hypospadias, Neuroblastoma, Mental retardation, Michelin tire baby syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Microstomia, Microtia, Motor delay, Multiple benign circumferential skin creases on limbs, Posteriorly rotated ear, Retinal diseases, Skin creases, congenital symmetric circumferentialView all (7 more) |
127
|
|
|
MiR-302/367 cluster host gene |
- |
|
128
|
|
|
Methionyl aminopeptidase 2 |
MAP2, MNPEP, p67eIF2 |
|
129
|
|
|
MIR4527 host gene |
- |
|
130
|
|
|
Midline 2 |
FXY2, MRX101, RNF60, TRIM1, XLID101 |
Attention deficit hyperactivity disorder, Autism, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Obesity, Seizure, Strabismus, Syndactyly of the toes |