Detailed description page of humcfs

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Humcfs_4714 details
Primary information
Humcfs IdHumcfs_4714
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000130175
gene_namePRKCSH
havana_transcript_idOTTHUMT00000458807
gene_location11435401-11436495
gene_orientation+
exon_idENSE00002882254, ENSE00003624440, ENSE00002781670
exon_number3
gene_descriptionprotein kinase C substrate 80K-H
disease_descriptionFenestration (morphologic abnormality),Seizures,Malignant neoplasm of stomach,Glioma,Liver cyst,Epilepsy, Temporal Lobe,Diabetes Mellitus, Insulin-Dependent,Carcinogenesis,Stomach Carcinoma,Colorectal Cancer,Hemiplegic migraine, familial type 1,Liver diseases,Polycystic liver disease,Colorectal Carcinoma,Situs Inversus,Polycystic Kidney Diseases,Cyst,Dysequilibrium syndrome,Non-Small Cell Lung Carcinoma,Breast Carcinoma,Polycystic Kidney, Autosomal Dominant
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank