Detailed description page of humcfs
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Humcfs_4901 details |
| Primary information | |
|---|---|
| Humcfs Id | Humcfs_4901 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000125650 |
| gene_name | PSPN |
| havana_transcript_id | OTTHUMT00000398031 |
| gene_location | 6375148-6379058 |
| gene_orientation | - |
| exon_id | ENSE00003183403 |
| exon_number | 1 |
| gene_description | persephin |
| disease_description | Hirschsprung Disease,Progressive supranuclear palsy,Pancreatitis,Prostate carcinoma,Malignant neoplasm of prostate,Impaired cognition,Pancreatic Ductal Adenocarcinoma,Multiple Endocrine Neoplasia Type 2a,Bipolar Disorder,Cerebral Infarction,Malignant neoplasm of mouth,Tauopathies,Cerebral Ischemia,Lip and Oral Cavity Carcinoma,Hirschsprung disease 1,Frontotemporal Lobar Degeneration |
| 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 |