Detailed description page of humcfs

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WDPCP details
Primary information
gene_nameWDPCP
Humcfs IdHumcfs_1098
chromosome_numberchromosome2
nameFRA2S
chrlocation44100001-154900000
cytoband2q23.3
typeAphidicolin
frequencyCommon
gene_ensembl_idENST00000409199
havana_transcript_idOTTHUMT00000326826
gene_location63121402-63477934
gene_orientation-
exon_idENSE00001189589, ENSE00003563027, ENSE00003602509, ENSE00003554041, ENSE00001070039, ENSE00001365513, ENSE00003640264, ENSE00003581314, ENSE00003493306, ENSE00003579927, ENSE00003691421, ENSE000015871
exon_number12
gene_descriptionWD repeat containing planar cell polarity effector
disease_descriptionOrstavik 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_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID20851513
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank