Detailed description page of humcfs

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Humcfs_4890 details
Primary information
Humcfs IdHumcfs_4890
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000198258
gene_nameUBL5
havana_transcript_idOTTHUMT00000450282
gene_location9827915-9830113
gene_orientation+
exon_idENSE00002896756, ENSE00002809142, ENSE00003661779, ENSE00002940847
exon_number4
gene_descriptionubiquitin-like 5
disease_descriptionHemophilia A,Fanconi Anemia,Metabolic Syndrome X,Coccidioidomycosis,Community acquired pneumonia,Adult T-Cell Lymphoma/Leukemia,Dermatitis, Phototoxic,Diabetes Mellitus,Tuberculosis, Multidrug-Resistant,HIV Infections,Malignant neoplasm of breast,Malignant neoplasm of pancreas,Breast Carcinoma,Coronary heart disease,Non-Small Cell Lung Carcinoma,Leukemia, T-Cell,FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Carcinoma of lung,Hemophilia, NOS,Malignant neoplasm of lung,Degenerative polyarthritis,Cystic Fibrosis,Tuberculosis,Mycoses,Diabetes,West Nile viral infection,Multiple Myeloma,Celiac Disease,Leukemia, Myelocytic, Acute,Hepatitis B,melanoma,Obesity,Dyslipidemias,Pancreatic carcinoma,Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site,MERRF Syndrome
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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