Detailed description page of humcfs

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Humcfs_3113 details
Primary information
Humcfs IdHumcfs_3113
chromosome_numberchromosome11
nameFRA11H
chrlocation63400001-77100000
cytoband11q13
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000149257
gene_nameSERPINH1
havana_transcript_idOTTHUMT00000383619
gene_location75562253-75566849
gene_orientation+
exon_idENSE00002149553, ENSE00002199517
exon_number2
gene_descriptionserpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
disease_descriptionDermatitis, Atopic,Malignant neoplasm of stomach,OSTEOGENESIS IMPERFECTA, TYPE X,Collagen-vascular disease,Stomach Carcinoma,Adult T-Cell Lymphoma/Leukemia,T-Cell Lymphoma,Fibrosis, Liver,Inflammation,Epidermolysis Bullosa Acquisita,Fibroid Tumor,Conjunctival scar,Coronary artery atheroma,Malignant neoplasm of breast,Ischemia,Breast Carcinoma,Cervical Squamous Cell Carcinoma,Liver Cirrhosis, Experimental,Hereditary gingival fibromatosis,Dermatologic disorders,Leukemia, T-Cell,Fetal Membranes, Premature Rupture,Coronary Arteriosclerosis,Connective Tissue Diseases,Plaque, Amyloid,Preterm premature rupture of membranes (disorder),Cardiovascular Diseases,Infection,Hepatitis B, Chronic,Autoimmune Diseases,Pregnancy Complications, Hematologic,Osteogenesis Imperfecta,Infarction, Middle Cerebral Artery,Liver Cirrhosis,Senile Plaques,Schistosomiasis,Nonspecific interstitial pneumonia,Tumor Progression,Central neuroblastoma,Hamman-Rich syndrome,Pheochromocytoma,Rheumatoid Arthritis,Fetal Disease
miRNA_location69083185-69083206
miRNA_strand+
miRNA_idMIMAT0015038
miRNA_namehsa-miR-3164
miRNA_derived MI0014194
TechniqueKaryotyping
PMID23852038
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