|
961
|
|
|
Maternal embryonic leucine zipper kinase |
HPK38 |
|
|
962
|
|
|
Microfibril associated protein 3 like |
NYD-sp9 |
|
|
963
|
|
|
Mediator complex subunit 24 |
ARC100, CRSP100, CRSP4, DRIP100, MED5, THRAP4, TRAP100 |
|
|
964
|
|
|
Membrane associated guanylate kinase, WW and PDZ domain containing 2 |
ACVRIP1, AIP-1, AIP1, ARIP1, MAGI-2, NPHS15, SSCAM |
Adenocarcinoma, Anxiety disorder, Bipolar disorder, Celiac disease, Diabetes mellitus, Epileptic encephalopathy, Genetic steroid-resistant nephrotic syndrome, Glomerulonephritis, Hypoalbuminemia, Inflammatory bowel disease, Irritable bowel syndrome, Major affective disorder, Memory disorders, Age-related memory disorders, Moyamoya disease, Nephrotic syndrome, Schizophrenia, West syndromeView all (3 more) |
|
965
|
|
|
Mannose receptor C-type 2 |
CD280, CLEC13E, ENDO180, UPARAP |
|
|
966
|
|
|
Mitofusin 2 |
CMT2A, CMT2A2, CMT2A2A, CMT2A2B, CPRP1, HMSN6A, HSG, MARF, MSL |
Axonal neuropathy, Charcot-marie-tooth disease, Dermatitis, Developmental delay, Diabetic nephropathy, Disorder of eye, Distal amyotrophy, Distal lower limb amyotrophy, Dysautonomia, Glomerulosclerosis, Hearing loss, Hereditary motor and sensory neuropathy, Hereditary motor and sensory neuropathy with optic atrophy, Hydrocephalus, Lipomatosis, Multiple lipomata, Multiple symmetric lipomatosis, Nail dystrophy, Nyctalopia, Optic atrophy, Partial paralysis vocal cords, Peripheral axonal atrophy, Peripheral axonal neuropathy, Restless legs syndrome, Saxonal neuropathy, Scoliosis, Spastic paraplegia, Vocal cord paralysisView all (13 more) |
|
967
|
|
|
MAF bZIP transcription factor B |
DURS3, KRML, MCTO |
Aniridia, Blepharophimosis, Blepharospasm, Brachydactyly, Congenital camptodactyly, Congenital clubfoot, Congenital coloboma of iris, Congenital hypoplasia of radius, Developmental delay, Duane retraction syndrome, Duane retraction syndrome with congenital deafness, Duane retraction syndrome with or without deafness, Duane syndrome, Duane-radial ray syndrome, Ectopic kidney, Fundus coloboma, Hearing loss, Hypertension, Hypoplasia of optic disc, Hypoplasia of the maxilla, Kidney disease, Microcephaly, Microcornea, Micrognathism, Multicentric carpo-tarsal osteolysis with or without nephropathy, Neck webbing, Nystagmus, Oculomotor nerve palsy, Multicentric carpo tarsal osteolysis with or without nephropathy, Osteopenia, Plagiocephaly, Polydactyly, Proptosis, Ptosis, Renal insufficiency, Retinal coloboma, Spina bifida occulta, Stenosis of external auditory canal, StrabismusView all (24 more) |
|
968
|
|
|
MAGE family member C1 |
CT7, CT7.1 |
|
|
969
|
|
|
Major vault protein |
LRP, VAULT1 |
|
|
970
|
|
|
Mediator complex subunit 12 |
ARC240, CAGH45, FGS1, HDKR, HOPA, Kto, MED12S, OHDOX, OKS, OPA1, TNRC11, TRAP230 |
Adrenocortical carcinoma, Agenesis of corpus callosum, Aortic coarctation, Arachnodactyly, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Blepharophimosis, Blepharophimosis-mental retardation syndrome, Brachycephaly, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Choanal atresia, Clinodactyly, Congenital camptodactyly, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Congenital malrotation of intestine, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Facial paralysis, Fg syndrome, Fibroadenoma, Frontal bossing, Gastric cancer, Gastroesophageal reflux disease, Hallucinations, Neurosensory hearing impairment, Hearing loss, High palate, Hirschsprung disease, Hydrocephalus, Hypoplasia of the maxilla, Hypoplasia of the optic nerve, Hypospadias, Imperforate anus, Mental retardation, Lujan-fryns syndrome, Lung carcinoma, Macrocephaly, Macrostomia, Cystosarcoma phyllodes, Malrotation of colon, Marfan syndrome, Meckel diverticulum, Mental depression, Mental retardation, x-linked, Micrognathism, Microstomia, Microtia, Mitral valve prolapse, Mood swings, Motor delay, Multiple congenital anomalies, Hypotonia, Neuronal heterotopia, Non-syndromic intellectual disability, x-linked, Nonorganic psychosis, Obesity, Obsessive-compulsive disorder, Ohdo syndrome, x-linked, Pancreatic adenocarcinoma, Partial agenesis of corpus callosum, Phyllodes tumor, Pierre-robin syndrome, Plagiocephaly, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Psychosis, Ptosis, Pulmonary arterial hypertension, Schizophrenia, Scoliosis, Seizure, Social communication disorder, Speech disorders, Stenosis of external auditory canal, Strabismus, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Thoracic aortic aneurysm and aortic dissection, Urogenital abnormalities, Ventricular septal defectView all (78 more) |
