Detailed description page of humcfs
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Humcfs_1157 details |
| Primary information | |
|---|---|
| Humcfs Id | Humcfs_1157 |
| chromosome_number | chromosome2 |
| name | FRA2S |
| chrlocation | 44100001-154900000 |
| cytoband | 2q23.3 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENST00000414712 |
| gene_name | PEX13 |
| havana_transcript_id | OTTHUMT00000325428 |
| gene_location | 61017730-61019080 |
| gene_orientation | + |
| exon_id | ENSE00001069926, ENSE00001675339 |
| exon_number | 2 |
| gene_description | peroxisomal biogenesis factor 13 |
| disease_description | Zellweger Spectrum,Zellweger Syndrome,Infantile Refsum Disease (disorder),Adrenoleukodystrophy,PEROXISOME BIOGENESIS DISORDER 11B,Peroxisome biogenesis disorders,Adrenoleukodystrophy, Neonatal,PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER),PEROXISOME BIOGENESIS DISORDER 2B,Cataract |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | Karyotyping |
| PMID | 20851513 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |