Detailed description page of humcfs

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Humcfs_4217 details
Primary information
Humcfs IdHumcfs_4217
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000105372
gene_nameRPS19
havana_transcript_idOTTHUMT00000463055
gene_location41860769-41869146
gene_orientation+
exon_idENSE00003138574, ENSE00003205369, ENSE00003198030
exon_number3
gene_descriptionribosomal protein S19
disease_descriptionSeizures,Congenital Abnormality,Fanconi Anemia,Idiopathic crescentic glomerulonephritis,Disease Progression,Muscle hypotonia,Congenital diaphragmatic hernia,Diamond-Blackfan Anemia 1,Severe Combined Immunodeficiency,arthritis symptoms,Decreased erythroid precursor production,Cervical dysplasia,Pure Red-Cell Aplasia,MYELODYSPLASTIC SYNDROME,Aplastic Anemia,Lupus Erythematosus, Systemic,Transient erythroblastopenia of childhood,Anemia, Diamond-Blackfan,Congenital Epicanthus,Experimental Autoimmune Encephalomyelitis,Stomach Neoplasms,Glaucoma, Open-Angle,Fetal anemia,Severe congenital neutropenia,FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Malaria,Lupus Erythematosus, Discoid,Absence Epilepsy,Polyarthritis,Hematological Disease,Arthritis,Schizophrenia,Congenital chromosomal disease,Preleukemia,Mouth Breathing,Pancytopenia,Arthritis, Collagen-Induced,Dyskeratosis Congenita,Anti-Glomerular Basement Membrane Disease,Enthesopathy,Lipoidosis,Anemia,bone destruction,Liver carcinoma,Thyro
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
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