Detailed description page of humcfs

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Humcfs_1230 details
Primary information
Humcfs IdHumcfs_1230
chromosome_numberchromosome3
nameFRA3C
chrlocation182700001-187900000
cytoband3q27
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000090539
gene_nameCHRD
havana_transcript_idOTTHUMT00000345497
gene_location184380207-184389829
gene_orientation+
exon_idENSE00001690943, ENSE00003643981, ENSE00003485221, ENSE00003526488, ENSE00003666150, ENSE00003592047, ENSE00003570841, ENSE00003666567, ENSE00000871259, ENSE00003560460, ENSE00003507055, ENSE000035793
exon_number23
gene_descriptionchordin
disease_descriptionShprintzen syndrome,Dissecting aneurysm of the thoracic aorta,22q11 Deletion Syndrome,Congenital Abnormality,ovarian neoplasm,Holoprosencephaly,Craniofacial Abnormalities,Mandibular hypoplasia,Mental handicap,Fibrodysplasia Ossificans Progressiva,Malignant neoplasm of ovary,DiGeorge Syndrome,Liver carcinoma,Cornelia De Lange Syndrome,Ovarian Carcinoma,Alcoholic Intoxication, Chronic
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID8406484
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