Detailed description page of humcfs

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Humcfs_4447 details
Primary information
Humcfs IdHumcfs_4447
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000167646
gene_nameDNAAF3
havana_transcript_idOTTHUMT00000392489
gene_location55162222-55166576
gene_orientation-
exon_idENSE00002176731, ENSE00003488094, ENSE00002862462, ENSE00003608619, ENSE00002165048
exon_number5
gene_descriptiondynein, axonemal, assembly factor 3
disease_descriptionCongenital Abnormality,Colorectal Cancer,Acquired CJD,airway disease,Autistic Disorder,Ciliary Motility Disorders,Neoplasm Metastasis,Thromboembolism,Neuroblastoma,Endometrial Carcinoma,Extramedullary Plasmacytoma,Protein C Deficiency,Situs Inversus,Neonatal purpura fulminans (homozygous protein C deficiency),Alzheimer's Disease,Uterine Corpus Cancer,Central neuroblastoma,Carcinogenesis,Hydrocephalus,Multiple Myeloma,Kartagener Syndrome,Pancreatic carcinoma,Colorectal Carcinoma,CILIARY DYSKINESIA, PRIMARY, 2 (disorder),Malignant neoplasm of pancreas,Prion Diseases,Malignant neoplasm of endometrium,Hormone refractory prostate cancer,Schizophrenia
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
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