Detailed description page of humcfs

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RET details
Primary information
gene_nameRET
Humcfs IdHumcfs_2888
chromosome_numberchromosome10
nameFRA10G
chrlocation42300001-52900000
cytoband10q11.2
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000165731
havana_transcript_idOTTHUMT00000358138
gene_location43077079-43127504
gene_orientation+
exon_idENSE00001155861, ENSE00001365997, ENSE00001095923, ENSE00001095946, ENSE00001095907, ENSE00001095904, ENSE00001312192, ENSE00001164816, ENSE00001164807, ENSE00001164798, ENSE00001164787, ENSE000010959
exon_number19
gene_descriptionret proto-oncogene
disease_descriptionPheochromocytoma, Extra-Adrenal,Undifferentiated carcinoma,Congenital Abnormality,Neuronal intestinal dysplasia,Non-Neoplastic Disorder,Drug Dependence,Adenocarcinoma of large intestine,Follicular adenoma,Malignant neoplasm of thyroid,Poorly Differentiated Thyroid Carcinoma,Rhabdoid Tumor of the Kidney,Medullary sponge kidney disease,Pituitary Neoplasms,Pleural Effusion, Malignant,HYPERPARATHYROIDISM 3,Nodular Goiter,Mammary Neoplasms,Developmental Disabilities,Benign Neoplasm,Neuroblastic Tumor,Primary Myelofibrosis,Myeloid Leukemia, Chronic,Follicular neoplasm,Hematopoietic Neoplasms,MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA,Parathyroid Gland Adenocarcinoma,Sleep Apnea, Obstructive,Nodule,Precancerous Conditions,Mucosal neuromas,Benign Struma Ovarii,Hashimoto Disease,Thyroiditis,Malignant tumor of colon,Urea Cycle Disorders, Inborn,Parathyroid Neoplasms,Prostatic Neoplasms,cancer recurrence,Multiple tumors,Pancreatic carcinoma,Leukemia, Myelocytic, Acute,Melanosis coli,
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID20101222
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