71
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|
|
WD repeat and FYVE domain containing 2 |
PROF, WDF2, ZFYVE22 |
Curated: N/A
Unreviewed: Anophthalmia, Bipolar disorder, Carcinogenesis, Malignant Neoplasm, Neoplasms, Ovarian cancer, Ovarian Carcinoma, Ovarian Epithelial carcinoma, Ovarian neoplasm, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms
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72
|
|
|
WD repeat and FYVE domain containing 3 |
ALFY, BCHS, MCPH18, ZFYVE25 |
Curated: Autism, Color vision deficiency, Neurodevelopmental disorder, Intellectual developmental disorder, Microcephaly, Non-specific syndromic intellectual disability, Oropharyngeal cancer, Schizophrenia, syndromic intellectual disability
Unreviewed: Arthritis, Ataxia, Brain disease, Cardiac Defects, Cerebral hemorrhage, Colorectal neoplasm, Double Outlet Right Ventricle, Ductal carcinoma, Esophageal neoplasm, Esophageal squamous cell carcinoma, Frontotemporal dementia, Gaucher disease, Glycogen storage disease, Huntington disease, Leukemia, Lymphatic metastasis, Macrocephaly, Malignant Neoplasm Of Lateral Wall Of Oropharynx, Malignant Neoplasm Of Oropharynx, Malignant tumor of posterior wall of oropharynx, Mental retardation, Myeloid leukemia, Myocardial infarction, Neurodevelopmental Disorders, Oropharyngeal Carcinoma, Parkinson disease, Periodontal disease, Promyelocytic Leukemia, Syndromic Mental Retardation, Triple negative breast cancer, Ventricular septal defect
|
73
|
|
|
WDFY3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
74
|
|
|
WDFY3 antisense RNA 2 |
C4orf12, FBI4, NCRNA00247 |
Curated: N/A
Unreviewed: Glioblastoma, Glioma, Neoplasms, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm
|
75
|
|
|
WDFY family member 4 |
C10orf64 |
Curated: Autism, Biliary cirrhosis, Neurodevelopmental disorder, Developmental disability, Inflammatory bowel disease, Non-specific syndromic intellectual disability, Biliary cholangitis, Colorectal cancer, Rheumatoid arthritis, Scoliosis, Stroke, Systemic lupus erythematosus, Ulcerative colitis
Unreviewed: Development Disorder, Lupus Erythematosus, Pancreatic ductal carcinoma
|
76
|
|
|
WD repeat and HMG-box DNA binding protein 1 |
AND-1, AND1, CHTF4, CTF4 |
Curated: Alzheimer disease, Astrocytoma, Dry eye syndrome, Parkinson disease, Peripheral neuropathy, Schizophrenia
Unreviewed: Adenoma, Alexander Disease, Amyloidosis, Anorexia, Anxiety Disorder, Asthma, Atherosclerosis, Atrial Fibrillation, Atrial Septal Defect, Autoimmune Diseases, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, Cardiovascular Diseases, Chromosomal instability, Chronic Obstructive Pulmonary Disease, Cognitive disorder, Colorectal adenoma, Congenital Contractural Arachnodactyly, Congestive Heart Failure, Corneal Dystrophy, Coronary Heart Disease, Cutaneous mastocytosis, Delirium, Dementia, Diabetes, Diabetes Insipidus, Diabetes Mellitus, Dyslipidemias, Endocrine System Diseases, Endometrial neoplasm, Esophageal Atresia, Esophageal squamous cell carcinoma, Gastric Cancer, Heart Failure, Hemophilia, Hepatocellular carcinoma, Hyperlipidemia, Hypertension, Hypospadias, Incontinentia Pigmenti Achromians, Inflammatory Bowel Disease, Kidney Disease, Kidney Failure, Left Ventricular Hypertrophy, Leukemia, Leukopenia, Lung Cancer, Lung carcinoma, Lung Diseases, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Melanoma, Mental Depression, Mental Disorders, Metabolic Syndrome, Metastatic Melanoma, Migraine with Aura, Myocardial Ischemia, Myopia, Nasopharyngeal carcinoma, Neoplasms, Neurogenic Urinary Bladder, Neuropathy, Neutropenia, Nonorganic Psychosis, Obesity, Optic Neuropathy, Osteopenia, Oxyphilic Adenoma, Periodontal Diseases, Periodontitis, Pharyngitis, Polyneuropathy, Pseudohyperkalemia Cardiff, Psoriasis, Psoriatic Arthritis, Psychosis, Sacroiliitis, Scleroderma, Senile Dementia, Skin Lesion, Spondyloarthritis, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Stress Disorder, Stroke, Thrombophilia, Triple negative breast cancer, Tumor, Vascular Diseases, XX Males
|
77
|
|
|
WD repeat containing planar cell polarity effector |
BBS15, C2orf86, CHDTHP, CPLANE5, FRITZ, FRTZ |
Curated: Alzheimer disease, Asthma, Astrocytoma, Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Bipolar disorder, Ciliopathy, Congenital heart disease, Melanoma, Developmental and epileptic encephalopathy, Aplasia of the vermis, Heart defect, tongue hamartoma and polysyndactyly, Insomnia, Major depressive disorder, Neurotic disorder, Obesity, Optic atrophy, Orofaciodigital syndrome, Prostate cancer, Retinitis pigmentosa, Substance abuse, Vesicoureteral reflux
Unreviewed: Anencephaly, Aortic Coarctation, Asplenia, Atrioventricular septal defect, Attention Deficit Hyperactivity Disorder, Bardet-Biedl Syndrome, Benign Neoplasm Of Nervous System, Cataract, Ciliopathies, Congenital Cerebral Hernia, Congenital Hepatic Fibrosis, Congenital Hypoplasia Of Penis, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Disorder Of Eye, Double Ureter, Dwarfism, Eczema, Fibrosis Of Pancreas, Foot Polydactyly, Hamartoma, Heart Defect, Tongue Hamartoma And Polysyndactyly, Hydrocephalus, Hypertension, Hypogonadism, Hypoplasia of the ovary, Liver cirrhosis, Liver Fibrosis, Lobar Holoprosencephaly, Male Pseudohermaphroditism, Malignant melanoma of skin, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Nephrotic Syndrome, Nystagmus, Optic Atrophy, Orstavik Lindemann Solberg Syndrome, Pancreatic Cyst, Patent ductus arteriosus, Polycystic liver disease, Polydactyly, Polysyndactyly, Postaxial hand polydactyly, Respiratory system infectious disease, Retinitis Pigmentosa, Sclerocornea, Sinusitis, Situs Inversus, Speech Disorders, Subaortic Stenosis, Syndactyly of fingers, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
|
78
|
|
|
WD repeat domain 1 |
AIP1, HEL-S-52, NORI-1, PFITS |
Curated: Atrial fibrillation, Dementia, Gout, Hoarding disorder, Hyperuricemia, Intellectual developmental disorder, Neurotic disorder, Osteoporosis, Parkinson disease, Thrombocytopenia
Unreviewed: Amyloidosis, Anaplastic thyroid cancer, Arteriosclerosis, Atherosclerosis, Atrial Fibrillation, Behcet Syndrome, Breast Cancer, Breast Carcinoma, Bulbospinal Atrophy, X-Linked, Cardiovascular disease, Cardiovascular Diseases, Cholangiocarcinoma, Cleft palate, Colorectal Cancer, Cyst, Esophagus Neoplasm, Frontotemporal dementia, Glioma, Gouty arthritis, Hemolytic uremic syndrome, Inflammatory Bowel Disease, Invasive Duct and Lobular Carcinoma, Kawasaki disease, Lung Cancer, Lung carcinoma, Lymphopenia, Macrothrombocytopenia, Melanoma, Neoplasms, Orofacial cleft, Papillary thyroid carcinoma, Paroxysmal atrial fibrillation, Respiratory system infectious disease, Schizophrenia, Skin ulcer, Stomatitis, Thyroid Neoplasm, Uranostaphyloschisis, Vascular Diseases
|
79
|
|
|
WD repeat domain 11 |
BRWD2, DR11, HH14, SRI1, WDR15 |
Curated: Anorexia nervosa, Nonsyndromic intellectual disability, Benign prostatic hyperplasia, Uinary system neoplasms, Breast cancer, Charge syndrome, Eating disorder, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Intellectual developmental disorder, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Prostate cancer, Schizophrenia, Sheehan syndrome, Diabetes mellitus type 2, Urogenital neoplasms
Unreviewed: Alopecia, Anodontia, Anxiety Disorder, Autism, Autoimmune hepatitis, Autoimmune Thyroiditis, Benign Prostatic Hyperplasia, Biliary Cirrhosis, Breast hypoplasia, Cartilage-Hair Hypoplasia, Celiac disease, Cholestasis of pregnancy, Ciliopathies, Cleft lip, Combined pituitary hormone deficiency, Congenital Camptodactyly, Congenital heart defect, Congenital Hypogonadotropic Hypogonadism, Congenital Hypoplasia Of Penis, Congenital ocular coloboma, Congenital Sensorineural Hearing Loss, Coronary artery disease, Cryptorchidism, Developmental Delay, Developmental disability, Diabetes Insipidus, Diabetes Mellitus, Diabetes mellitus, type 1, Dwarfism, Dysarthria, End Stage Liver Disease, Erectile Dysfunction, Female Hypogonadism Syndrome, Glioblastoma, Glioma, Graves Disease, Growth disorder, Gynecomastia, Hashimoto Disease, Hearing Loss, Hemochromatosis, Hereditary Hemochromatosis, Holoprosencephaly, Hypoglycemia, Hypogonadism, Hypogonadotropic Hypogonadism, Hypogonadotropic Hypogonadism With Or Without Anosmia, Hypoplasia of the ovary, Hypospadias, Hypothyroidism, Ichthyosis, Inflammatory Myopathy, Intestinal Obstruction, Juvenile arthritis, Kallmann Syndrome, Kidney Disease, Kidney Failure, Lupus Erythematosus, Lupus Nephritis, Lymphocytic Leukemia, Malignant Neoplasm, Medulloblastoma, Melanoma, Mental Depression, Mental retardation, Microcephaly, Mirror Movements, Multiple Sclerosis, Myeloid Leukemia, Myocardial infarction, Neoplasms, Non-obstructive azoospermia, Normosmic Congenital Hypogonadotropic Hypogonadism, Nystagmus, Obesity, Osteoarthritis, Osteochondrodysplasia, Osteopenia, Osteoporosis, Papillary thyroid carcinoma, Paraplegia, Pemphigus, Penis Agenesis, Physiologic Amenorrhea, Pituitary Stalk Interruption Syndrome, Psoriasis, Ptosis, Renal agenesis, Rheumatic Heart Disease, Rheumatoid arthritis, Sarcoidosis, Scleroderma, Sclerosing Cholangitis, Secondary Physiologic Amenorrhea, Septo-Optic Dysplasia, Skeletal Dysplasia, Stomach Carcinoma, Testicular Hypogonadism, Thymoma, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Vasculitis
|
80
|
|
|
WDR11 divergent transcript |
WDR11-AS1 |
Curated: N/A
Unreviewed: N/A
|