4351
|
|
|
EYA transcriptional coactivator and phosphatase 1 |
BOP, BOR, BOS1, OFC1, OTFCS |
Anhydramnios, Anterior segment dysgenesis, Asymmetric crying face association, Autism, Bell's palsy, Bor syndrome, Branchiooculofacial syndrome, Branchiootic syndrome, Branchiootorenal syndrome, Cayler cardiofacial syndrome, Obstructive pulmonary disease, Conductive hearing loss, Congenital abnormalities, Renal agenesis, Congenital heart defects, Congenital hypoplasia of kidney, Craniofacial abnormalities, Dental caries, Endometriosis, Focal glomerulosclerosis, Glaucoma, Hearing impairment, Congenital heart defect, Hypospadias, Large artery stroke, Myasthenia gravis, Major depressive disorder, Metabolic syndrome, Colorectal adenoma, Migraine, Nonalcoholic fatty liver disease, Oligodendroglioma, Otofaciocervical syndrome, Pelvic organ prolapse, Peptic ulcer disease, Scoliosis, Diabetes mellitus type 2View all (22 more) |
4352
|
|
|
EYA transcriptional coactivator and phosphatase 2 |
EAB1 |
Asthma, Attention deficit hyperactivity disorder, Glaucoma, Insomnia, Metabolic syndrome, Myelodysplastic syndrome, Nonalcoholic fatty liver disease, Open angle glaucoma, Osteoarthritis, Otosclerosis, Respiratory system disease, Schizophrenia, Scoliosis, Seasonal allergic rhinitis, Diabetes mellitus type 2 |
4353
|
|
|
EYA transcriptional coactivator and phosphatase 4 |
CMD1J, DFNA10 |
Alzheimer disease, Asthma, Atrial fibrillation, Isolated sensorineural deafness, Nonsyndromic hearing loss, Dilated cardiomyopathy, Cardiomyopathy, Colorectal neoplasms, Congestive heart failure, Deafness, Gastroesophageal reflux disease, Hearing impairment, Hearing loss, Heart failure, Hereditary hearing loss, Left ventricular noncompaction cardiomyopathy, Sensorineural deafness with dilated cardiomyopathyView all (2 more) |
4354
|
|
|
Eyes shut homolog |
C6orf178, C6orf179, C6orf180, EGFL10, EGFL11, RP25, SPAM, bA166P24.2, bA307F22.3, bA74E24.1, dJ1018A4.2, dJ22I17.2, dJ303F19.1 |
Anterior uveitis, Astigmatism, Retinitis pigmentosa, Central areolar choroidal dystrophy, Colorectal cancer, Cone-rod dystrophy, Dyschromatopsia, Endometriosis, Retinopathy, Generalized anxiety disorder, Insomnia, Macular dystrophy, Major depressive disorder, Melanoma, Migraine, Mood disorder, Optic atrophy, Osteoarthritis, Ovarian cancer, Ovarian serous carcinoma, Retinal detachment, Retinitis punctata albescens, Rod-cone dystrophy, Schizophrenia, Scoliosis, Stargardt disease, Systemic mastocytosis, Hypertension, Diabetes mellitus type 1, Diabetes mellitus type 2View all (15 more) |
4355
|
|
|
Enhancer of zeste 1 polycomb repressive complex 2 subunit |
KMT6B |
|
4356
|
|
|
Enhancer of zeste 2 polycomb repressive complex 2 subunit |
ENX-1, ENX1, EZH2b, KMT6, KMT6A, WVS, WVS2 |
Breast neoplasms, Hepatocellular carcinoma, Congenital abnormalities, Congestive heart failure, Craniosynostosis, Desbuquois syndrome, Endometrial neoplasms, Gout, Heart failure, Lymphoma, Diffuse large b-cell lymphoma, Myelodysplastic syndrome, Neurodevelopmental disorder, Osteosarcoma, Ovarian neoplasms, Prostatic neoplasms, Squamous cell carcinoma, Upper extremity deformity, congenital, Weaver syndromeView all (4 more) |
4357
|
|
|
EZH inhibitory protein |
CATACOMB, CXorf67, KIP75 |
|
4358
|
|
|
Ezrin |
CVIL, CVL, HEL-S-105, VIL2 |
|
4359
|
|
|
Coagulation factor X |
FX, FXA |
|
4360
|
|
|
Coagulation factor XI |
FXI, PTA |
Thromboembolic pulmonary hypertension, Coagulation factor deficiency syndrome, Congenital factor xi deficiency, Cor pulmonale, Coronary artery disease, Factor xi deficiency, Heart disease, Hypertension, Intracranial thrombosis, Thrombocytopenia, Thrombophilia, Venous thromboembolism |
