Gene Information
|
Gene Name
|
GALNT17 |
|
Gene ID
|
64409
|
|
Gene Full Name
|
polypeptide N-acetylgalactosaminyltransferase 17 |
|
Gene Alias
|
GALNACT17|GALNT16|GALNT20|GALNTL3|GalNAc-T17|GalNAc-T19|GalNAc-T5L|WBSCR17 |
|
Transcripts
|
ENSG00000185274
|
|
Virus
|
HTLV1 |
|
Gene Type
|
protein-coding |
|
HPA Location Info
|
Nucleoplasm, Golgi apparatus;Nucleoli, Nuclear bodies; 
|
|
Membrane Info
|
Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins |
|
Uniport_ID
|
Q6IS24
|
|
HGNC ID
|
HGNC:16347
|
|
OMIM ID
|
615137 |
|
Summary
|
This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013] |
Target gene [GALNT17] related to VISs 
Integration Table: if previous studies reported that target gene was altered by virus integration events, the overlap between VISs in this literature and Cistrome factors was listed in this section
| DVID |
Chromosome |
HM |
TFBS |
CA |
Sum of Overlapped Records |
Detail |
| 6005515 |
chr7 |
1 |
36 |
49 |
86 |
View |
| 6023656 |
chr7 |
2 |
2 |
0 |
4 |
View |
| 6024150 |
chr7 |
4 |
0 |
0 |
4 |
View |
| 6027565 |
chr7 |
2 |
0 |
0 |
2 |
View |
Target gene [GALNT17] related to Omics data
| Data ID |
Experiment type |
Sample number |
Platform |
|
GSE52244
|
Expression array |
15 |
[HuEx-1_0-st] Affymetrix Human Exon 1.0 ST Array [probe set (exon) version] |
|
C GSE94732
|
Chip-seq |
24 |
Illumina NextSeq 500 (Homo sapiens);illumina Genome Analyzer IIx (Homo sapiens) |
When the gene can detect a peak in the dataset, a peak plot will be displayed.
> Dataset: GSE94732 - GALNT17 peak across samples
|
Peak Plot
|
|
|
HTLV1 Target gene Detail Information
