|
721
|
|
|
Motile sperm domain containing 1 |
DJ473B4 |
|
|
722
|
|
|
Melanocortin 2 receptor accessory protein |
B27, C21orf61, FALP, FGD2, GCCD2, MRAP1 |
Adrenal hypoplasia, x-linked, Anorexia, Azoospermia, Congenital hypothyroidism, Cryptorchidism, Glucocorticoid deficiency, Hypernatriuria, Hypertrophic cardiomyopathy, Hypoglycemic coma, Hypoglycemic seizures, Mental retardation, Precocious puberty, Quadriplegia, Testicular adrenal rest tumor |
|
723
|
|
|
MBL associated serine protease 1 |
3MC1, CRARF, CRARF1, MAP-1, MAP1, MASP, MASP-3, MASP3, MAp44, PRSS5, RaRF |
3mc syndrome, Accessory nipple, Amyotrophic lateral sclerosis, Atrial septal defect, Blepharophimosis, Camptodactyly of fingers, Congenital exomphalos, Congenital omphalocele, Conjunctival telangiectasis, Coronal craniosynostosis, Craniofacial ulnar renal syndrome, Craniosynostosis, Cryptorchidism, Diabetes mellitus, Glaucoma, Hearing loss, Hydronephrosis, Incontinentia pigmenti achromians, Lateral sclerosis, Malpuech facial clefting syndrome, Mental retardation, Microcephaly, Oral cleft, Patent ductus arteriosus, Pigmentation disorders, Ptosis, Radioulnar synostosis, Scoliosis, Spina bifida occulta, Synostotic posterior plagiocephaly, Talipes transversoplanus, Ventricular septal defectView all (17 more) |
|
724
|
|
|
Matrix metallopeptidase 26 |
- |
|
|
725
|
|
|
MAP3K7 C-terminal like |
C21orf7, HC21ORF7, TAK1L, TAKL, TAKL-1, TAKL-2, TAKL-4 |
|
|
726
|
|
|
Methylcrotonyl-CoA carboxylase subunit 1 |
MCC-B, MCCA, MCCCalpha |
|
|
727
|
|
|
Mitochondrial ribosomal protein S22 |
C3orf5, COXPD5, GIBT, GK002, MRP-S22, ODG7, RPMS22, mS22 |
46, xx gonadal dysgenesis, 46, xx gonadal sex reversal, 46,xx gonadal dysgenesis, Alopecia, Alopecia, male pattern, Androgenetic alopecia, Arachnodactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Combined oxidative phosphorylation deficiency, Dwarfism, Gonadal dysgenesis, Hypertrophic cardiomyopathy, Hypoplasia of corpus callosum, Hypotonia with lactic acidemia and hyperammonemia, Leukoencephalopathy, Marfan syndrome, Microcephaly, Movement disorders, Obesity, Osteopenia, Osteoporosis of vertebrae, Ovarian adenocarcinoma, Ovarian dysgenesis, Physiologic amenorrhea, Posteriorly rotated ear, Premature menopause, Pulmonary fibrosis, Secondary physiologic amenorrhea, Spastic quadriplegia, Streak ovaryView all (17 more) |
|
728
|
|
|
Mitochondrial fission factor |
C2orf33, EMPF2, GL004 |
Astigmatism, Cerebellar atrophy, Colorectal cancer, Developmental delay, Dysphagia, Encephalopathy, External ophthalmoplegia, Microcephaly, Mitochondrial encephalomyopathy, Myocardial infarction, Nervous system diseases, Optic atrophy |
|
729
|
|
|
Matrix extracellular phosphoglycoprotein |
OF45 |
|
|
730
|
|
|
Mannosidase alpha class 1C member 1 |
HMIC, MAN1A3, MAN1C, pp6318 |
|
