Detailed description page of humcfs

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WFS1 details
Primary information
gene_nameWFS1
Humcfs IdHumcfs_1301
chromosome_numberchromosome4
nameFRA4A
chrlocation6000001-11300000
cytoband4p16.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000109501
havana_transcript_idOTTHUMT00000358732
gene_location6289075-6300917
gene_orientation+
exon_idENSE00002087052, ENSE00003648875, ENSE00003689853, ENSE00002027543, ENSE00002042563
exon_number5
gene_descriptionWolfram syndrome 1 (wolframin)
disease_descriptionSeizures,Nonsyndromic Deafness,Optic Atrophy, Autosomal Dominant,Disorder of the optic nerve,nervous system disorder,Diabetic Ketoacidosis,Metabolic Syndrome X,Unipolar Depression,Autistic Disorder,Nuclear non-senile cataract,WAARDENBURG SYNDROME, TYPE IIA,Hearing problem,HIV Infections,Lung Neoplasms,Cataract, Nuclear Total,Headache,DEAFNESS, AUTOSOMAL DOMINANT 6,Mental Depression,Sensorineural Hearing Loss (disorder),Nuclear cataract,Diabetes Mellitus, Insulin-Dependent,Gestational Diabetes,Diabetic Nephropathy,psychiatric hospitalization,Hearing Loss,Hyperinsulinism,Polydipsia,Diabetes Mellitus, Non-Insulin-Dependent,Diabetes,Central Diabetes Insipidus,Wolfram-Like Syndrome, Autosomal Dominant,Completed Suicide,Autoimmune Diseases,Major Depressive Disorder,CATARACT 41,hearing impairment,Prediabetes syndrome,Mood Disorders,Post-Traumatic Stress Disorder,Hearing Loss, Partial,Neurodegenerative Disorders,Depressive disorder,Parkinson Disease,Diabetes Mellitus,Obesity,Mental disorders,D
miRNA_location10078622-10078645
miRNA_strand-
miRNA_idMIMAT0015006
miRNA_namehsa-miR-3138
miRNA_derived MI0014161
TechniqueKaryotyping
PMID17567780
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