192241
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WAP four-disulfide core domain 2 |
BENP, EDDM4, HE4, WAP5, dJ461P17.6 |
Curated: Bronchiectasis
Unreviewed: Breast neoplasm, Carcinogenesis, Carcinoma, Carcinoma in situ, Colorectal Cancer, Colorectal neoplasm, Cystic fibrosis, Cystic lung disease, Ductal carcinoma of breast, Endometrial Cancer, Endometrial carcinoma, Endometrial hyperplasia, Endometrial neoplasm, Endometrioid carcinoma, Epithelial ovarian carcinoma, Heart disease, Heart failure, Hyperglycemia, Hypoxia, Idiopathic pulmonary fibrosis, Kidney Disease, Lung Cancer, Lung carcinoma, Lung disease, Lung neoplasms, Lymphatic metastasis, Lymphedema, Malignant Neoplasm, Mesothelioma, Multiple Sclerosis, Nasal polyp, Nasopharyngeal carcinoma, Neoplasms, Ovarian cancer, Ovarian Carcinoma, Ovarian cysts, Ovarian diseases, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic neoplasm, Pancreatitis, Periodontitis, Peritoneal neoplasm, Pituitary Diseases, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Pulmonary hypertension, Respiratory Failure, Sjogren syndrome, Small cell lung carcinoma, Stomach neoplasms, Transitional cell carcinoma, Ulcerative colitis, Uterine neoplasm, Uterine polyp
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192242
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WAP four-disulfide core domain 21, pseudogene |
LNCDC, linc-DC, lnc-DC |
Curated: N/A
Unreviewed: Colorectal Cancer, Colorectal neoplasm, Coronary artery disease, Multiple sclerosis, Rheumatoid arthritis, Sjogren syndrome, Systemic lupus erythematosus
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192243
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WAP four-disulfide core domain 3 |
WAP14, dJ447F3.3 |
Curated: N/A
Unreviewed: Colorectal neoplasm, Pancreatic neoplasm
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192244
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WAP four-disulfide core domain 5 |
PRG5, WAP1, dJ211D12.5 |
Curated: Bipolar disorder
Unreviewed: Melanoma, Neoplasms
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192245
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WAP four-disulfide core domain 6 |
C20orf171, HEL-S-295, WAP6, dJ461P17.11 |
Curated: N/A
Unreviewed: N/A
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192246
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WAP four-disulfide core domain 8 |
C20orf170, HEL-S-292, WAP8, dJ461P17.1 |
Curated: N/A
Unreviewed: N/A
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192247
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WAP four-disulfide core domain 9 |
WAP9, dJ688G8.2 |
Curated: N/A
Unreviewed: N/A
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192248
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WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1 |
C16orf12, RJD2, WFDC20A, WFIKKN |
Curated: N/A
Unreviewed: Urinary bladder neoplasms
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192249
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WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 |
GASP-1, WFDC20B, WFIKKNRP, hGASP-1 |
Curated: Diverticular disease
Unreviewed: N/A
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192250
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Wolframin ER transmembrane glycoprotein |
CTRCT41, WFRS, WFS, WFSL |
Curated: Auditory neuropathy, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Bipolar disorder, Cataract, Congenital cataract, Deafness, Major depressive disorder, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Diabetic eye disease, Diabetic neuropathy, Diabetic polyneuropathy, Diabetic retinopathy, Nuclear cataract, Hearing loss, Heart failure, Hereditary hearing loss, Meniere disease, Metabolic syndrome, Mood disorder, Optic atrophy, Other specified diabetes mellitus with unspecified complications, Perisylvian syndrome, Retinitis pigmentosa, Spastic ataxia, Diabetic nephropathy type 2, Wolfram syndrome, Wolfram-like syndrome, nonsyndromic genetic hearing loss
Unreviewed: Alstrom syndrome, Anemia, Anxiety Disorder, Aortic Valve Insufficiency, Arachnodactyly, Ataxia, Attention deficit hyperactivity disorder, Autoimmune disease, Autoimmune Diseases, Bipolar Disorder, Blindness, Blood Coagulation Disorders, Cardiomyopathy, Cerebellar Ataxia, Cerebral Atrophy, Cerebral cortical atrophy, Chronic obstructive pulmonary disease, Color vision deficiency, Colorectal neoplasm, Congenital anomalies of the kidney and urinary tract, Congenital hemidysplasia with ichthyosiform erythroderma and limb defects, Congenital Sensorineural Hearing Loss, Costeff optic atrophy syndrome, Crohn disease, Dandy-Walker Syndrome, Dementia, Developmental Delay, Developmental regression, Diabetes, Diabetes Insipidus, Diabetes Mellitus, Diabetes mellitus transient neonatal, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Diabetic Ketoacidosis, Diabetic Nephropathy, Diaphragmatic Eventration, Dilated cardiomyopathy, Disorder Of Eye, Disruptive, impulse control, and conduct disorders, Dysarthria, Dysautonomia, Dysphagia, Dyssomnia, Endometrial neoplasm, Eye disease, Gastric ulcer, Glaucoma, Graves Disease, Growth disorder, Hallucinations, Headache, Hearing Loss, Hereditary neuropathy with liability to pressure palsies, Hodgkin Disease, Hydronephrosis, Hyperaldosteronism, Hyperglycemia, Hyperinsulinism, Hypertension, Hypoglycemia, Hypothyroidism, Insulinoma, Keratosis Follicularis, Kidney Disease, Laryngomalacia, Low-frequency hearing loss, Lung Neoplasms, Major Affective Disorder, Malabsorption Syndrome, Mason type diabetes, Mental Depression, Mental Disorders, Mental retardation, Metabolic Syndrome, Microglossia, Micrognathism, Microspherophakia, Mitochondrial disease, Mitochondrial Diseases, Mood Disorder, Mucolipidosis, Myopathy, Myotonic dystrophy, Nervous system disease, Nervous System Diseases, Neurodegenerative disorder, Neurodegenerative Disorders, Neurogenic Urinary Bladder, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Nyctalopia, Nystagmus, Obesity, Optic Atrophy, Optic Neuropathy, Osteoarthritis, Parkinson disease, Peptic Ulcer, Peptic ulcer disease, Peripheral axonal neuropathy, Polycystic Ovary Syndrome, Psychosis, Ptosis, Retinal detachment, Retinitis Pigmentosa, Sideroblastic Anemia, Sleep Apnea, Sleep Disorders, Tauopathies, Testicular atrophy, Testicular Hypogonadism, Thiamine Deficiency, Thiamine Responsive Megaloblastic Anemia Syndrome, Thiamine-responsive megaloblastic anemia, Thyroid cancer, Trichohepatoenteric Syndrome, Uranostaphyloschisis, Usher Syndrome, Vestibular disease, Visual disorder, Waardenburg Syndrome, Wolf-Hirschhorn Syndrome, Wolfram Syndrome, Wolfram-Like Syndrome
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