Detailed description page of humcfs

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Humcfs_2869 details
Primary information
Humcfs IdHumcfs_2869
chromosome_numberchromosome10
nameFRA10G
chrlocation42300001-52900000
cytoband10q11.2
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000185532
gene_namePRKG1
havana_transcript_idOTTHUMT00000048105
gene_location51153279-52062863
gene_orientation+
exon_idENSE00001766763, ENSE00001311075, ENSE00001319764, ENSE00001295696, ENSE00003487488, ENSE00003602134, ENSE00001462050
exon_number7
gene_descriptionprotein kinase, cGMP-dependent, type I
disease_descriptionAttention deficit hyperactivity disorder,Aortic Aneurysm, Thoracic,Malignant neoplasm of stomach,Asthma,Hyper-IgM Immunodeficiency Syndrome, Type 1,acute aortic dissection,Decompression Sickness,Sezary Syndrome,Schistosomiasis,Spinal Muscular Atrophy,Growth Hormone-Secreting Pituitary Adenoma,Erectile dysfunction,Pulmonary Hypertension,MYELODYSPLASTIC SYNDROME,Deficiency of phosphoglycerate kinase,Anemia, Hemolytic,Hereditary sideroblastic anemia,Malignant neoplasm of breast,Tobacco Use Disorder,Coronary heart disease,Adenoma,Pain,Papilloma, Intraductal,Coronary Arteriosclerosis,Leukodystrophy, Metachromatic,Phosphoglycerate Kinase 1 Deficiency,Cardiovascular Diseases,Myocardial Ischemia,As If Personality,Mucopolysaccharidoses,Blood pressure finding,Amphetamine-Related Disorders,Breast Carcinoma,Precancerous Conditions,Dissecting aneurysm of the thoracic aorta,Lymphoma,Phyllodes Tumor,Brain Ischemia,Cerebrovascular accident,X-Linked Lymphoproliferative Disorder,Hypogonadism,Cerebral He
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID20101222
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