Detailed description page of humcfs

This page displays user query in tabular form.

Humcfs_4228 details
Primary information
Humcfs IdHumcfs_4228
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000075702
gene_nameWDR62
havana_transcript_idOTTHUMT00000457437
gene_location36054990-36071562
gene_orientation+
exon_idENSE00001804790, ENSE00003699148, ENSE00001606439, ENSE00003702285, ENSE00003700548, ENSE00003697091, ENSE00003697976, ENSE00003701607, ENSE00002867967
exon_number9
gene_descriptionWD repeat domain 62
disease_descriptionAutosomal Recessive Primary Microcephaly,Hypoplasia of corpus callosum,Malonic aciduria,Congenital Abnormality,Congenital anomaly of brain,Carcinogenesis,Intellectual Disability,Neurodevelopmental Disorders,Mild Mental Retardation,Stomach Carcinoma,Microlissencephaly,Malignant neoplasm of stomach,MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder),Microcephaly,Macular dystrophy, corneal type 1,Kuzniecky syndrome,Primary microcephaly
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank