Primary information |
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gene_name | CHERP |
Humcfs Id | Humcfs_5048 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000085872 |
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 |