| Primary information |
|---|
| Humcfs Id | Humcfs_1098 |
| chromosome_number | chromosome2 |
| name | FRA2S |
| chrlocation | 44100001-154900000 |
| cytoband | 2q23.3 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENST00000409199 |
| gene_name | WDPCP |
| havana_transcript_id | OTTHUMT00000326826 |
| gene_location | 63121402-63477934 |
| gene_orientation | - |
| exon_id | ENSE00001189589, ENSE00003563027, ENSE00003602509, ENSE00003554041, ENSE00001070039, ENSE00001365513, ENSE00003640264, ENSE00003581314, ENSE00003493306, ENSE00003579927, ENSE00003691421, ENSE000015871 |
| exon_number | 12 |
| gene_description | WD repeat containing planar cell polarity effector |
| disease_description | Orstavik Lindemann Solberg syndrome,Meckel-Gruber syndrome,Heart defect, tongue hamartoma and polysyndactyly,BARDET-BIEDL SYNDROME 15,Atrial Fibrillation,Bardet-Biedl Syndrome,Polysyndactyly,Obesity,Hamartoma of tongue |
| 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 |