Detailed description page of humcfs
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Humcfs_3973 details |
Primary information | |
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Humcfs Id | Humcfs_3973 |
chromosome_number | chromosome18 |
name | FRA18B |
chrlocation | 53800001-61600000 |
cytoband | 18q21.3 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENSG00000081923 |
gene_name | ATP8B1 |
havana_transcript_id | OTTHUMT00000450459 |
gene_location | 57731775-57740965 |
gene_orientation | - |
exon_id | ENSE00002970530, ENSE00002736665 |
exon_number | 2 |
gene_description | ATPase, aminophospholipid transporter, class I, type 8B, member 1 |
disease_description | Idiopathic chronic pancreatitis,Colorectal Cancer,Pruritus,Cholestasis,Diarrhea,Liver diseases,Alagille Syndrome,Dwarfism,Benign recurrent intrahepatic cholestasis,Diarrheal disorder,Cholera,Vitiligo,Attention Deficit and Disruptive Behavior Disorders,Cystic Fibrosis,Neonatal hepatitis,Intrahepatic Cholestasis,Cholestatic liver disease,Liver Failure,Hepatoblastoma,Colorectal Carcinoma,Cholestasis of pregnancy,Progressive intrahepatic cholestasis (disorder),CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1,Pancreatitis,Cholestasis, chronic,Pancreatitis, Chronic,Malabsorption Syndrome,Hearing Loss, Mixed Conductive-Sensorineural |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 25238782 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |