Detailed description page of humcfs

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Humcfs_3029 details
Primary information
Humcfs IdHumcfs_3029
chromosome_numberchromosome11
nameFRA11E
chrlocation31000001-36400000
cytoband11p13
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000007372
gene_namePAX6
havana_transcript_idOTTHUMT00000389013
gene_location31801745-31812177
gene_orientation-
exon_idENSE00003602163, ENSE00002523992, ENSE00001098662, ENSE00001004114
exon_number4
gene_descriptionpaired box 6
disease_descriptionCongenital Abnormality,Bladder Neoplasm,Tooth Abnormalities,Congenital hypoplasia,Congenital ptosis,Fanconi Anemia,O'Donnell Pappas syndrome,Photophobia,Cleft Palate,Axenfeld-Rieger Syndrome, Type 1,Glaucoma of childhood,Retinal Degeneration,Noninfiltrating Intraductal Carcinoma,Cardiomyopathy, Familial Idiopathic,Pituitary dwarfism,Mood Disorders,Keratoconjunctivitis Sicca,Diabetes Mellitus,Obesity,Mental disorders,Exudative retinopathy,Presenile cataract,Adenomatous Polyposis Coli,Posterior embryotoxon,Astrocytoma,Keratitis,Smith-Lemli-Opitz Syndrome,Cerebral atrophy,Tobacco Use Disorder,Morning glory syndrome,Corneal Diseases,Urogenital Abnormalities,Low Vision,Intellectual Disability,Rieger syndrome,Colorectal Cancer,Disorder of the optic nerve,Foveal Hypoplasia, Isolated,Dry Eye Syndromes,Prostate carcinoma,Corneal pannus,Refractive Errors,Gillespie syndrome,Pituitary Diseases,Anterior segment mesenchymal dysgenesis,Malignant neoplasm of breast,Breast Carcinoma,Disorder of eye,Tra
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID16511518
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