Detailed description page of humcfs

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Humcfs_3168 details
Primary information
Humcfs IdHumcfs_3168
chromosome_numberchromosome11
nameFRA11H
chrlocation63400001-77100000
cytoband11q13
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000175544
gene_nameCABP4
havana_transcript_idOTTHUMT00000397667
gene_location67452415-67459228
gene_orientation+
exon_idENSE00002276954, ENSE00002250598, ENSE00002301738, ENSE00001186018, ENSE00001186007, ENSE00001185997, ENSE00001287586
exon_number7
gene_descriptioncalcium binding protein 4
disease_descriptionNight blindness, congenital stationary,Night Blindness,Retinal Diseases,NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder),Neuroblastoma
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID23852038
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank