Primary information |
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Humcfs Id | Humcfs_2607 |
chromosome_number | chromosome10 |
name | FRA10A |
chrlocation | 97000000-1089500001 |
cytoband | 10q23.3 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000108039 |
gene_name | XPNPEP1 |
havana_transcript_id | OTTHUMT00000050253 |
gene_location | 109882548-109907819 |
gene_orientation | - |
exon_id | ENSE00001642640, ENSE00003506415, ENSE00003543665, ENSE00003557752, ENSE00003510669, ENSE00003613899, ENSE00001769426 |
exon_number | 7 |
gene_description | X-prolyl aminopeptidase (aminopeptidase P) 1, soluble |
disease_description | Cerebrovascular accident,Central neuroblastoma,Adenomatous Polyposis Coli,Neuroblastoma,Carcinogenesis,Coughing,Neurofibrillary degeneration (morphologic abnormality),Tobacco Use Disorder,Biliary Atresia,Senile Plaques,Down Syndrome,Alzheimer's Disease,Crohn Disease |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 3879149 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |