Primary information |
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gene_name | WDPCP |
Humcfs Id | Humcfs_1098 |
chromosome_number | chromosome2 |
name | FRA2S |
chrlocation | 44100001-154900000 |
cytoband | 2q23.3 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENST00000409199 |
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 |