Detailed description page of humcfs

This page displays user query in tabular form.

Humcfs_4836 details
Primary information
Humcfs IdHumcfs_4836
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000133246
gene_namePRAM1
havana_transcript_idOTTHUMT00000460327
gene_location8499196-8502634
gene_orientation-
exon_idENSE00003085832, ENSE00002980934, ENSE00001795838
exon_number3
gene_descriptionPML-RARA regulated adaptor molecule 1
disease_descriptionadult acute promyelocytic leukemia (M3),Neoplasm, Residual,Chromosome 8, trisomy,Hereditary pancreatitis,Rheumatoid Arthritis,Refractory cancer,leukemia,Acute Promyelocytic Leukemia,Myeloid Leukemia,childhood acute promyelocytic leukemia (M3),Leukemogenesis,Promyelocytic leukemia,Leukemia, Myelocytic, Acute,Congenital chromosomal disease,Acute leukemia,Leukoencephalopathy, Progressive Multifocal,Multiple Myeloma,Thrombocythemia, Essential
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank