Detailed description page of humcfs

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GPI details
Primary information
gene_nameGPI
Humcfs IdHumcfs_4145
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000105220
havana_transcript_idOTTHUMT00000451690
gene_location34365022-34377578
gene_orientation+
exon_idENSE00002863299, ENSE00003698305, ENSE00003787300, ENSE00003698198, ENSE00003697707, ENSE00002877518
exon_number6
gene_descriptionglucose-6-phosphate isomerase
disease_descriptionLupus Erythematosus, Systemic,HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY,Congenital diaphragmatic hernia,Nephrotoxic serum nephritis,Congenital chromosomal disease,Anemia, Hemolytic,HIV Infections,Paracoccidioidomycosis,Lupus Erythematosus, Discoid,Myeloid Leukemia, Chronic,Mammary Neoplasms,Pancytopenia,Senile Plaques,Chronic active hepatitis,Rheumatoid Arthritis,Abdominal Pain,Pancreatic carcinoma,Non-Malignant Ascites Adverse Event,Acute monocytic leukemia,Myeloid Leukemia,Lupus Erythematosus,Morphologically altered structure,Polyendocrinopathies, Autoimmune,Acquired aplastic anemia,Limb ischemia,Colorectal Cancer,Atypical Hemolytic Uremic Syndrome,Secondary malignant neoplasm of liver,Aplastic Anemia,Malignant neoplasm of breast,Ischemia,Experimental Autoimmune Encephalomyelitis,Rheumatic Fever,Malaria,Malignant hyperpyrexia due to anesthesia,Polyarthritis,Upper Respiratory Infections,Anemia, Hemolytic, Congenital,Chagas Disease,Paroxysmal noctu
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
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