|
871
|
|
|
Mediator complex subunit 28 |
1500003D12Rik, EG1, magicin |
|
|
872
|
|
|
Megakaryocyte and platelet inhibitory receptor G6b |
C6orf25, G6b, G6b-B, NG31, THAMY |
|
|
873
|
|
|
Microfibril associated protein 5 |
AAT9, MAGP-2, MAGP2, MFAP-5, MP25 |
Aortic aneurysm, Aortic valve insufficiency, Arachnodactyly, Bicuspid aortic valve, Breast cancer, Congenital pectus carinatum, Congenital pectus excavatum, Coronary arteriosclerosis, Cutis marmorata, Descending aortic dissection, Dyspnea, paroxysmal, Hypertension, Ischemic stroke, Patent ductus arteriosus, Peripheral arterial stenosis, Scoliosis, Subarachnoid hemorrhage, Thoracic aortic aneurysm and aortic dissection, Transient ischemic attackView all (4 more) |
|
874
|
|
|
Myeloid leukemia factor 2 |
NTN4 |
|
|
875
|
|
|
MOB kinase activator 2 |
HCCA2 |
|
|
876
|
|
|
Mucosal vascular addressin cell adhesion molecule 1 |
MACAM1 |
|
|
877
|
|
|
Mediator complex subunit 25 |
ACID1, ARC92, BVSYS, CMT2B2, P78, PTOV2, TCBAP0758 |
Absence of septum pellucidum, Autism, Basel-vanagaite-smirin-yosef syndrome, Blepharophimosis, Cataract, Central visual impairment, Cerebral atrophy, Charcot-marie-tooth disease, Congenital epicanthus, Cortical dysplasia, Developmental delay, Distal amyotrophy, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Hypospadias, Mental retardation, Mental depression, Microcephaly, Microcornea, Motor delay, Nevus, Non-syndromic intellectual disability, Polymicrogyria, Posteriorly rotated ear, Ptosis, Salaam seizures, Seizure, Sleep disorders, Stereotyped behavior, StrabismusView all (16 more) |
|
878
|
|
|
MIA SH3 domain containing |
CD-RAP, MIA1 |
|
|
879
|
|
|
MKKS centrosomal shuttling protein |
BBS6, HMCS, KMS, MKS |
Atresia of vagina, Atrial septal defect, Bardet-biedl syndrome, Brachydactyly, Ciliopathies, Developmental dysplasia of the hip, Pulmonary hypoplasia, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes mellitus, Disorder of eye, Dwarfism, Ectopic anus, Foot polydactyly, High palate, Hirschsprung disease, Hydrometrocolpos, Hydronephrosis, Hypertension, Hypogonadism, Hypoplastic left heart syndrome, Hypospadias, Imperforate anus, Kaufman-mckusick syndrome, Liver fibrosis, Mckusick-kaufman syndrome, Mental retardation, Multicystic renal dysplasia, Nephrotic syndrome, Nystagmus, Obesity, Patent ductus arteriosus, Polycystic kidney disease, Polydactyly, Progressive cone dystrophy, Renal cyst, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly, Syndactyly of fingers, Tarsal coalition, Tetralogy of fallot, Postaxial hand polydactyly, Ventricular septal defect, Vesicovaginal fistulaView all (33 more) |
|
880
|
|
|
MAX dimerization protein 3 |
BHLHC13, MAD3, MYX |
|
