Detailed description page of humcfs

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PIGV details
Primary information
gene_namePIGV
Humcfs IdHumcfs_32
chromosome_numberchromosome1
nameFRA1A
chrlocation1-28000000
cytoband1p36
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000060642
havana_transcript_idOTTHUMT00000011703
gene_location26788098-26794396
gene_orientation+
exon_idENSE00001694565, ENSE00003476293, ENSE00001780863
exon_number3
gene_descriptionphosphatidylinositol glycan anchor biosynthesis, class V
disease_descriptionHirschsprung Disease,Seizures,Vitamin B 6 Deficiency,Congenital Abnormality,Congenital malformation syndrome,Congenital anomaly of the kidney,Intellectual Disability,Hyperphosphatasia with Mental Retardation,ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1,Hirschsprung disease 1,Mental Retardation
miRNA_location187931-187953
miRNA_strand-
miRNA_idMIMAT00276181
miRNA_namehsa-miR-6859-5p
miRNA_derived MI0026420
TechniqueKaryotyping
PMID1322577
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