Detailed description page of humcfs

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ABCC8 details
Primary information
gene_nameABCC8
Humcfs IdHumcfs_2981
chromosome_numberchromosome11
nameFRA11C
chrlocation16200001-21700000
cytoband11p15.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000006071
havana_transcript_idOTTHUMT00000389093
gene_location17392885-17476845
gene_orientation-
exon_idENSE00003692076, ENSE00003479439, ENSE00003558999, ENSE00003528254, ENSE00003557574, ENSE00001607229, ENSE00001742580, ENSE00003673102, ENSE00003467114, ENSE00003669416, ENSE00003636670, ENSE000036741
exon_number39
gene_descriptionATP-binding cassette, sub-family C (CFTR/MRP), member 8
disease_descriptionFasting Hypoglycemia,Congenital Hyperinsulinism,DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder),Fanconi-Bickel Syndrome,Cardiovascular Diseases,Gestational Diabetes,Mucocutaneous Lymph Node Syndrome,Sleep Apnea, Obstructive,Senile Plaques,Metabolic Syndrome X,Diabetes, Autoimmune,Pancreatic Ductal Adenocarcinoma,Rheumatoid Arthritis,Hypoglycemia,Congenital hemihypertrophy,Diabetes Mellitus, Transient Neonatal, 1,Cardiac defects,Diabetes Mellitus,Obesity,Neonatal diabetes mellitus,Kidney Failure, Chronic,Pseudomonas aeruginosa infection,Abdominal sepsis,Sepsis,Keratitis,Neonatal disorder,Myeloid Leukemia,Alzheimer's Disease,Leukemia, B-Cell,Tumor necrosis,insulinoma,Seizures,Acute Promyelocytic Leukemia,Malignant neoplasm of breast,Breast Carcinoma,Vasculitis,Diabetes Mellitus, Insulin-Dependent,Adenoma,Hyperinsulinism,Impaired glucose tolerance,Leukopenia,Bacterial keratitis,Nesidioblastosis,Peritonitis,Hypoglycemia, leucine-induced,Dermatomyositis, Childhood Type,Papilloma,Congest
miRNA_location19760013-19760033
miRNA_strand-
miRNA_idMIMAT0019787
miRNA_namehsa-miR-4694-3p
miRNA_derived MI0017327
TechniqueKaryotyping
PMID15771901
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank
Primary information
gene_nameABCC8
Humcfs IdHumcfs_3297
chromosome_numberchromosome11
nameFRA11I
chrlocation16100001-21600000
cytoband11p15.1
typeDistamycinA
frequencyRare
gene_ensembl_idENSG00000006071
havana_transcript_idOTTHUMT00000389093
gene_location17392885-17476845
gene_orientation-
exon_idENSE00002167112, ENSE00001764780, ENSE00003502854, ENSE00003595999, ENSE00003687298, ENSE00003509263, ENSE00003458902, ENSE00003467886, ENSE00002182754, ENSE00003489184, ENSE00003543819, ENSE000016330
exon_number13
gene_descriptionATP binding cassette subfamily C member 8
disease_description
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID3169734
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank