| Primary information |
|---|
| gene_name | PEX1 |
| Humcfs Id | Humcfs_2041 |
| chromosome_number | chromosome7 |
| name | FRA7E |
| chrlocation | 91100001-92800000 |
| cytoband | 7q21.2 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENSG00000127980 |
| havana_transcript_id | OTTHUMT00000342657 |
| gene_location | 92487020-92528441 |
| gene_orientation | - |
| exon_id | ENSE00001748791, ENSE00003620142, ENSE00003614712, ENSE00003529841, ENSE00003651842, ENSE00003671483, ENSE00003594027, ENSE00003687712, ENSE00003659773, ENSE00003562198, ENSE00003671296, ENSE000036834 |
| exon_number | 21 |
| gene_description | peroxisomal biogenesis factor 1 |
| disease_description | Peroxisomal Disorders,Zellweger Spectrum,Infantile Refsum Disease (disorder),Zellweger Syndrome,nervous system disorder,Leber Congenital Amaurosis,Peroxisome biogenesis disorders,Adrenoleukodystrophy, Neonatal,Fatty Liver,PEROXISOME BIOGENESIS DISORDER 2B,Deafness enamel hypoplasia nail defects |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | FISH |
| PMID | 14517285 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |