|
481
|
|
|
Midline 1 |
BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY |
Agenesis of corpus callosum, Congenital heart defects, Cryptorchidism, Developmental delay, Dysphagia, Frontal bossing, Gastroesophageal reflux disease, High palate, Hypospadias, Imperforate anus, Opitz gbbb syndrome, x-linked |
|
482
|
|
|
Macrophage migration inhibitory factor |
GIF, GLIF, MMIF |
Anaplastic carcinoma, Anxiety disorder, Arthritis, Autism, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Colitis, Malignant mesothelioma, Marfan syndrome, Melancholia, Memory disorders, Age-related memory disorders, Mental depression, Pericarditis, Pleural effusion, Prostatic neoplasms, Prostate cancer, Rheumatoid arthritis, Septicemia, Stevens-johnson syndrome, Still disease, UveitisView all (9 more) |
|
483
|
|
|
Major intrinsic protein of lens fiber |
AQP0, CTRCT15, LIM1, MIP26, MP26 |
|
|
484
|
|
|
Mitochondrial intermediate peptidase |
COXPD31, HMIP, MIP |
Ankyloglossia, Arnold-chiari malformation, Cardiomyopathy, Cerebral palsy, Choreoathetosis, Combined oxidative phosphorylation deficiency, Congenital cataract, Developmental delay, Eczema, Esotropia, Hyperopia, Hypertrophic cardiomyopathy, Laryngomalacia, Left ventricular noncompaction, Lipoma, Maternal hypertension, Myopia, Optic atrophy, Phakomatosis pigmentovascularisView all (4 more) |
|
485
|
|
|
Melanocyte inducing transcription factor |
CMM8, COMMAD, MI, MITF-A, WS2, WS2A, bHLHe32 |
Albinism, Ocular albinism with sensorineural deafness, Anomalous pulmonary artery, Attention deficit hyperactivity disorder, Atypical mole melanoma syndrome, Mammary neoplasms, Hereditary cancer syndrome, Chromophobe carcinoma, Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness, Congenital ocular coloboma, Congenital sensorineural hearing loss, Deafness, Frontal bossing, Hearing loss, Hereditary paraganglioma-pheochromocytoma syndromes, Hirschsprung disease, Hyperopia, Hypopigmentation disorder, Incontinentia pigmenti achromians, Intestinal obstruction, Macrocephaly, Melanoma, Cutaneous malignant melanoma, Mental retardation, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Multiple lentigines, Nevus, Nystagmus, Ocular albinism, Ocular albinism with congenital sensorineural deafness, Oculocutaneous albinism, Tyrosinase-negative oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism, Osteopetrosis, Pancreatic neoplasm, Papillary renal carcinoma, Piebaldism, Pigmentation disorders, Poliosis, Posteriorly rotated ear, Ptosis, Renal carcinoma, Retinal diseases, Sensorineural hearing loss, Speech disorders, Stomach neoplasms, Strabismus, Synophrys, Tietz syndrome, Waardenburg syndromeView all (37 more) |
|
486
|
|
|
Marker of proliferation Ki-67 |
KIA, MIB-, MIB-1, PPP1R105 |
Adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Liver carcinoma, Copper-overload cirrhosis, Marfan syndrome, Mesenchymal chondrosarcoma, Nervous system diseases, Ovarian neoplasm, Ovarian cancer, Palmoplantar pustules, PsoriasisView all (2 more) |
|
487
|
|
|
Muskelin 1 |
TWA2 |
|
|
488
|
|
|
Myeloid leukemia factor 1 |
- |
|
|
489
|
|
|
MutL homolog 1 |
COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1, MMRCS1, hMLH1 |
Adenocarcinoma of duodenum, Adenoma sebaceum, Agnosia, Anxiety disorder, Astrocytoma, Attention deficit hyperactivity disorder, Benign digestive system neoplasms, Benign genitourinary tract neoplasm, Benign neoplasm of nervous system, Brain neoplasms, Breast cancer, Breast carcinoma, Hereditary cancer syndrome, Carcinoma, Cardiac diverticulum, Central nervous system neoplasms, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Constitutional mismatch repair deficiency syndrome, Developmental regression, Dysarthria, Dysgraphia, Dyskinetic syndrome, Endometrial cancer, Endometrial carcinoma, Ependymoma, Gastric cancer, Genitourinanry tract tumors, Glioblastoma, Hallucinations, Hematologic neoplasms, Hemiplegia/hemiparesis, Hereditary breast and ovarian cancer syndrome, Hereditary nonpolyposis colorectal cancer, Intestinal polyposis, Kidney neoplasm, Laryngeal carcinoma, Leukemia, Liver neoplasms, Liver carcinoma, Lung adenocarcinoma, Lymphoma, Lynch syndrome, Malabsorption syndrome, Malignant neoplasm of the central nervous system, Medulloblastoma, Mental depression, Migraine, Muir-torre syndrome, Neoplasm of skeletal system, Neuroblastoma, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Pancreatic adenocarcinoma, Pituitary adenoma, Polyp of large intestine, Prostatic neoplasms, Prostate cancer, Rectal neoplasms, Rhabdomyosarcoma, Salivary gland neoplasm, Sarcoma, Sebaceous adenocarcinoma, Stomach neoplasms, Thyroid neoplasm, Torre-muir syndrome, Turcot syndrome, Urologic neoplasmsView all (55 more) |
|
490
|
|
|
Mitogen-activated protein kinase kinase kinase 9 |
MEKK9, MLK1, PRKE1 |
|
