Detailed description page of humcfs

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Humcfs_4814 details
Primary information
Humcfs IdHumcfs_4814
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000088256
gene_nameGNA11
havana_transcript_idOTTHUMT00000452296
gene_location3114947-3115428
gene_orientation+
exon_idENSE00002943395, ENSE00002797454
exon_number2
gene_descriptionguanine nucleotide binding protein (G protein), alpha 11 (Gq class)
disease_descriptionUterine Corpus Cancer,Hypocalciuric hypercalcemia, familial, type 1,Desmoplastic melanoma,Epithelioid and spindle cell nevus,Pituitary Diseases,Neoplasm Metastasis,Malignant neoplasm of breast,HYPOCALCEMIA, AUTOSOMAL DOMINANT 2,Polyglandular Type I Autoimmune Syndrome,melanoma,Nevus, Blue,Hyperparathyroidism, Primary,Hyperparathyroidism,Endometrial Carcinoma,Uveal melanoma,Multiple Sclerosis,Tumor Progression,aggressive cancer,Monosomy,Nevus,Congenital Heart Defects,Malignant Mesothelioma of Peritoneum,Familial benign hypercalcemia,Malignant neoplasm of endometrium,Cutaneous Melanoma,Hypercalcemia,Hypoparathyroidism - autosomal dominant,HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder),Uveal Neoplasms
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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