Detailed description page of humcfs
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Humcfs_4714 details |
Primary information | |
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Humcfs Id | Humcfs_4714 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000130175 |
gene_name | PRKCSH |
havana_transcript_id | OTTHUMT00000458807 |
gene_location | 11435401-11436495 |
gene_orientation | + |
exon_id | ENSE00002882254, ENSE00003624440, ENSE00002781670 |
exon_number | 3 |
gene_description | protein kinase C substrate 80K-H |
disease_description | Fenestration (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_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | FISH |
PMID | 3568428 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |