Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "V"
31 to 40 of 99 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

31
Visual system homeobox 2
CHX10, HOX10, MCOP2, MCOPCB3, RET1
Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Blindness, Breast cancer, Colobomatous microphthalmia, Crohn disease, Human papillomavirus infection, Inflammatory bowel disease, Microphthalmia, Microphthalmos, Ocular sarcoidosis, Retinitis pigmentosa, Ulcerative colitis

32
Von Willebrand factor A domain containing 2
AMACO, CCSP-2, CCSP2, NET42
Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Oligodendroglioma, Vesicular stomatitis

33
Vestigial like family member 3
VGL-3, VGL3
Attention deficit hyperactivity disorder, Breast cancer, Diabetic ketoacidosis, Obesity, Prostate cancer, Diabetes mellitus, type 2

34
Von Willebrand factor A domain containing 5A
BCSC-1, BCSC1, LOH11CR2A

35
Von Willebrand factor C domain containing 2 like
-
Insomnia, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Schizophrenia, Diabetes mellitus, type 2

36
Vitrin
VIT1
Cerebral artery occlusion, Hypertrophic cardiomyopathy, Leprosy, Metabolic syndrome, Oligodendroglioma, Osteoarthritis, Ovarian serous carcinoma, Peripheral arterial disease, Schizophrenia, Stroke, Diabetes mellitus, type 2, Upper aerodigestive tract neoplasm

37
Vacuolar protein sorting 13 homolog C
BLTP5C, PARK23
Parkinson disease, Bipolar disorder, Diabetic retinopathy, Hemiparkinsonism, Intellectual developmental disorder, Metabolic syndrome, Oligodendroglioma, Alzheimer disease, Schizophrenia, Diabetes mellitus, type 2, Young-onset parkinson disease

38
VPS37C subunit of ESCRT-I
-
Breast benign neoplasm, Hypothyroidism, Rheumatoid arthritis, Scoliosis

39
Vacuolar protein sorting 13 homolog D
BLTP5D, SCA24, SCAR4, SCASI
Arthrogryposis multiplex congenita, Spinocerebellar ataxia, Atrophic gastritis, Cerebellar ataxia, Central nervous system cancer, Cholecystolithiasis, Glioblastoma, Glioma, Non-immune hydrops fetalis, Leigh syndrome, Neurodevelopmental disorders, Pena-shokeir syndrome type i, Psychiatric disorders

40
Vertebrae development associated
C14orf115, vertnin
Alzheimer disease, Atrial fibrillation, Cardiac embolism, Cardioembolic stroke