|
181
|
|
|
MDS1 and EVI1 complex locus |
AML1-EVI-1, EVI1, KMT8E, MDS1, MDS1-EVI1, PRDM3, RUSAT2 |
Amegakaryocytic thrombocytopenia, Anemia, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Cardiovascular diseases, Colonic neoplasms, Congenital thrombocytopenia, Coronary heart disease, Glaucoma, Hearing loss, Leukemia, Lymphoid leukemia, Marfan syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Myeloid leukemia, Myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2), Myeloproliferative disorder, Nasopharyngeal neoplasms, Nasopharyngeal cancer, Nasopharyngeal carcinoma, Neutropenia, Osteoporosis, Ovarian neoplasm, Ovarian cancer, Pancytopenia, Prostate cancer, Prostate cancer, hereditary, Radioulnar synostosis, Radioulnar synostosis with amegakaryocytic thrombocytopenia, Syndactyly of fingers, Testicular hydroceleView all (20 more) |
|
182
|
|
|
Membrane spanning 4-domains A2 |
APY, ATOPY, FCER1B, FCERI, IGEL, IGER, IGHER |
|
|
183
|
|
|
Membrane associated ring-CH-type finger 8 |
CMIR, MARCH-VIII, MARCH8, MIR, RNF178, c-MIR |
|
|
184
|
|
|
Mitogen-activated protein kinase 15 |
ERK7, ERK8 |
|
|
185
|
|
|
Muscle RAS oncogene homolog |
M-RAs, NS11, R-RAS3, RRAS3 |
Abnormal dermatoglyphic pattern, Atrial septal defect, Brachydactyly, Camptodactyly of fingers, Cardiofaciocutaneous syndrome, Cardiovascular diseases, Carotid artery disease, Carotid atherosclerosis, Congenital pectus carinatum, Congenital pectus excavatum, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Costello syndrome, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Dysarthria, Hearing loss, High palate, Hypogonadotropic hypogonadism, Leopard syndrome, Cystic hygroma, Melanocytic nevus, Micrognathism, Moyamoya disease, Narcolepsy, Neck webbing, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Nystagmus, Posteriorly rotated ear, Proptosis, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Scoliosis, StrabismusView all (24 more) |
|
186
|
|
|
MLX interacting protein |
MIR, MONDOA, bHLHe36 |
|
|
187
|
|
|
MORC family CW-type zinc finger 2 |
CMT2Z, DIGFAN, ZCW3, ZCWCC1 |
Camptodactyly of fingers, Charcot-marie-tooth disease, Congenital pectus excavatum, Cutis marmorata, Developmental delay, Dysautonomia, Exophoria, Glabellar hemangioma, Hereditary motor and sensory neuropathy, Multiple congenital anomalies, Oral aversion, Roussy-levy syndrome |
|
188
|
|
|
Multimerin 1 |
ECM, EMILIN4, GPIa*, MMRN |
|
|
189
|
|
|
Microtubule associated protein RP/EB family member 1 |
EB1 |
|
|
190
|
|
|
Microtubule associated protein RP/EB family member 3 |
EB3, EBF3, EBF3-S, RP3 |
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