Detailed description page of humcfs

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TCHP details
Primary information
gene_nameTCHP
Humcfs IdHumcfs_3604
chromosome_numberchromosome12
nameFRA12E
chrlocation109000001-133851895
cytoband12q24
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000139437
havana_transcript_idOTTHUMT00000403290
gene_location109900609-109906637
gene_orientation+
exon_idENSE00002220985, ENSE00003543703, ENSE00003494830, ENSE00000938151, ENSE00002283066
exon_number5
gene_descriptiontrichoplein, keratin filament binding
disease_descriptionHemangioblastoma,Cervix carcinoma,Liver and Intrahepatic Biliary Tract Carcinoma,Osteosarcoma of bone,Malignant neoplasm of kidney,Benign Neoplasm,Mammary Neoplasms,Endometrial Carcinoma,Parathyroid Gland Adenocarcinoma,Precancerous Conditions,Malignant tumor of colon,Pancreatic Ductal Adenocarcinoma,Pancreatic carcinoma,Leukemia, Myelocytic, Acute,Myeloblastic leukemia,Giant Cell Tumors,Latent virus infection phase,Brain Neoplasms,Meningioma, benign, no ICD-O subtype,Myeloid Leukemia,Kaposi Sarcoma,Differentiated Thyroid Gland Carcinoma,Malignant tumor of cervix,Colorectal Cancer,Meningioma,Prostate carcinoma,Acute Promyelocytic Leukemia,Triple Negative Breast Neoplasms,Malignant neoplasm of breast,Breast Carcinoma,Hereditary gingival fibromatosis,Neuroblastoma,Adenocarcinoma of prostate,Renal Cell Carcinoma,Hereditary Breast and Ovarian Cancer Syndrome,CHARGE Syndrome,Congenital ear anomaly NOS (disorder),Tumor Progression,Malignant neoplasm of liver,Central neuroblastoma,Multiple En
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID14526166
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