Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14651 to 14660 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14651
Von Willebrand factor C domain containing 2
PSST739, UNQ739
Alzheimer disease, Hyperopia, Insomnia, Keratoconus, Metabolic syndrome, Obesity, Psoriatic arthritis, Diabetes mellitus type 2

14652
Von Willebrand factor C domain containing 2 like
-
Insomnia, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Schizophrenia, Diabetes mellitus type 2

14653
Von Willebrand factor D and EGF domains
-
Angioedema, Coronary artery disease, Frontotemporal dementia, Generalized anxiety disorder, Heart failure, Insomnia, Major depressive disorder, Optic atrophy, Post-traumatic stress disorder

14654
Von Willebrand factor
F8VWF, VWD
Atrial fibrillation, Autism, Behcet disease, Bernard-soulier syndrome, Cardiovascular disease, Cerebral thrombosis, Congestive heart failure, Coronary artery disease, Crohn disease, Exanthema, Heart disease, Heart failure, Hemophilia a, Hypertension, Intracranial thrombosis
View all (14 more)

14655
Vexin
C8orf46
Color vision deficiency, Prostate cancer, Scoliosis

14656
WW domain containing adaptor with coiled-coil
BM-016, DESSH, PRO1741, Wwp4
Alzheimer disease, Desanto-shinawi syndrome, Facial dysmorphism syndrome, Multiple myeloma, Neurodevelopmental disorder, Prostatic neoplasms

14657
WAPL cohesin release factor
FOE, KIAA0261, WAPAL
Cardiovascular disease, Color vision deficiency, Neurodevelopmental disorder, Congenital clubfoot, Hypertension, Migraine, Non-specific syndromic intellectual disability, Amyotrophic lateral sclerosis, Diabetes mellitus type 2, Ventricular septal defect

14658
Tryptophanyl-tRNA synthetase 1
GAMMA-2, HMN9, HMND9, IFI53, IFP53, NEDMSBA, WARS
Primary microcephaly, Charcot-marie-tooth disease, Developmental delay, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Schizophrenia, Scoliosis, Papillary thyroid cancer

14659
Tryptophanyl tRNA synthetase 2, mitochondrial
NEMMLAS, PKDYS3, TrpRS, mtTrpRS
Androgenetic alopecia, Major depressive disorder, Mitochondrial disease, Neurodevelopmental disorder, Obstructive sleep apnea syndrome, Osteoarthritis, Parkinsonism-dystonia, Sialolithiasis, Combined oxidative phosphorylation defect

14660
WASP actin nucleation promoting factor
IMD2, SCNX, THC, THC1, WASP, WASPA
Severe congenital neutropenia, Thrombocytopenia, Wiskott-aldrich syndrome, X-linked severe congenital neutropenia, X-linked thrombocytopenia