Detailed description page of humcfs

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Humcfs_3174 details
Primary information
Humcfs IdHumcfs_3174
chromosome_numberchromosome11
nameFRA11H
chrlocation63400001-77100000
cytoband11q13
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000133895
gene_nameMEN1
havana_transcript_idOTTHUMT00000105354
gene_location64803516-64810716
gene_orientation-
exon_idENSE00001473564, ENSE00003685663, ENSE00003617827, ENSE00001171239, ENSE00001171248, ENSE00001171254, ENSE00003789012, ENSE00001312579, ENSE00001298138, ENSE00001473560
exon_number10
gene_descriptionmultiple endocrine neoplasia I
disease_descriptionIslet Cell Tumor,Enterochromaffin-like cell carcinoid,Glucagonoma,Cervix carcinoma,Adult T-Cell Lymphoma/Leukemia,Pituitary Neoplasms,Angiofibroma,Atypical carcinoid tumor,Malignant tumor of cervix,Esophageal Gastrointestinal Stromal Tumor,HIV Infections,Well Differentiated Pancreatic Endocrine Tumor,Adrenal hyperplasia,Coronary heart disease,Benign symmetrical lipomatosis,McCune-Albright Syndrome,pancreatic gastrinoma,ovarian neoplasm,Cardiovascular Diseases,Hematopoietic Neoplasms,Gastritis, Atrophic,Parathyroid Gland Adenocarcinoma,Steatohepatitis,Adrenocortical hyperplasia,Parathyroid Neoplasms,Prostatic Neoplasms,Hypoglycemia,Multiple tumors,Pancreatic carcinoma,Fibrous skin tumor of tuberous sclerosis,Diabetes Mellitus,Adrenal hypertrophy or hyperplasia,Primary Lesion,Kidney Failure, Chronic,Smooth Muscle Tumor,Thyroid Neoplasm,Adrenocortical carcinoma,Meningioma, benign, no ICD-O subtype,Skin Neoplasms,Colonic Neoplasms,Carcinoid Tumor,insulinoma,Leydig Cell Tumor,Leydig cell tu
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID23852038
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