| Primary information |
|---|
| Humcfs Id | Humcfs_5048 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000085872 |
| gene_name | CHERP |
| havana_transcript_id | OTTHUMT00000403372 |
| gene_location | 16517896-16542415 |
| gene_orientation | - |
| exon_id | ENSE00002345493, ENSE00003559233, ENSE00003576469, ENSE00003666164, ENSE00003518605, ENSE00003515488, ENSE00003635090, ENSE00003542976, ENSE00000873470, ENSE00000687040, ENSE00000687043, ENSE000024252 |
| exon_number | 17 |
| gene_description | calcium homeostasis endoplasmic reticulum protein |
| disease_description | Chronic Obstructive Airway Disease,Congenital anomaly of skeletal bone,Skeletal malformation,Promyelocytic leukemia,Leprosy, Lepromatous,nervous system disorder,leukemia,Acute Promyelocytic Leukemia,Leprosy, Paucibacillary,Schizophrenia,CAMPOMELIC DYSPLASIA |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | FISH |
| PMID | 3568428 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |