Detailed description page of humcfs

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FECH details
Primary information
gene_nameFECH
Humcfs IdHumcfs_3967
chromosome_numberchromosome18
nameFRA18B
chrlocation53800001-61600000
cytoband18q21.3
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000066926
havana_transcript_idOTTHUMT00000449862
gene_location57554259-57586690
gene_orientation-
exon_idENSE00002789462, ENSE00003686289, ENSE00003492409, ENSE00003487393, ENSE00000669629, ENSE00003484710, ENSE00003610599, ENSE00002926861
exon_number8
gene_descriptionferrochelatase
disease_descriptionIron deficiency,Liver diseases,Acute Erythroblastic Leukemia,PHOTOPAROXYSMAL RESPONSE 1,Porphyria, Erythropoietic,Malignant neoplasm of breast,Fibrosis,Secondary acquired sideroblastic anemia,Myelodysplasia,Myeloid Leukemia,Bile Duct Diseases,Malaria,Variegate Porphyria,Erythropoietic Protoporphyria,Breast Carcinoma,Hepatobiliary disease,Anemia,Chronic myeloproliferative disorder,Malignant tumor of colon,Acute intermittent porphyria,Cholestatic liver disease,Metabolic Diseases,Liver Failure,Disorders of Porphyrin Metabolism,Inherited disorder of porphyrin metabolism,Colorectal Carcinoma,Myeloproliferative disease,Preleukemia,Skin-ache syndrome,Glioma,Keratoderma,Porphyrias, Hepatic,Glioblastoma,Tobacco Use Disorder,Burning sensation,Colon Carcinoma
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID25238782
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