Symbol
| SLC39A4
| contributors: snh - updated : 23-02-2009
|
HGNC name
| solute carrier family 39 (zinc transporter), member 4
|
HGNC id
| 17129
|
corresponding disease(s)
|
AEZ
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
|  
| --over
|  
|
significantly higher in pancreatic cancer cells than pancreatic ductal epithelium | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
|
System | Type | Disorder | Pubmed |
cancer | digestive | pancreas | |
targeted to control pancreatic cancer growth |
| | | |
| bovine hereditary zinc deficiency has a clinical presentation similar to acrodermatitis enteropathica in humans |