Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 6569 |
Gene Name: | solute carrier family 34 member 1 |
Gene Aliases: |
FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2 |
Location: |
Chr.5:177384431-177412021 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC34A1 | NM_001167579.1 | NP_001161051.1 | ||
| NM_003052.4 | NP_003043.3 | |||
| XM_005265975.1 | XP_005266032.1 | |||
| XM_017009773.1 | XP_016865262.1 | |||
| XM_017009775.1 | XP_016865264.1 | |||
| AK096088.1 | BAC04699.1 | |||
| AK298299.1 | ||||
| BC035294.1 | ||||
| BC050385.1 | AAH50385.1 | |||
| BC053349.1 | AAH53349.1 | |||
| L13258.1 | AAA36354.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv471057 | Chr.5:177310308 - 177469411 on Build GRCh38 | Loss |
 PRR7
GRK6
F12
PRR7-AS1
LMAN2
SLC34A1
MXD3
PFN3
RGS14
DBN1
|
| nsv509103 | Chr.5:177308751 - 177414575 on Build GRCh38 | Insertion |
F12
LMAN2
SLC34A1
MXD3
PFN3
RGS14
|
| nsv600364 | Chr.5:177299634 - 177432847 on Build GRCh38 | Loss |
PRELID1
GRK6
F12
LMAN2
SLC34A1
MXD3
NSD1
PFN3
RAB24
RGS14
|
| dgv10184n54 | Chr.5:177357511 - 177469411 on Build GRCh38 | Loss |
PRR7
GRK6
F12
PRR7-AS1
SLC34A1
PFN3
RGS14
DBN1
|
| nsv1161313 | Chr.5:177356552 - 177463415 on Build GRCh38 | Duplication |
PRR7
GRK6
F12
PRR7-AS1
SLC34A1
PFN3
RGS14
DBN1
|
| nsv1161312 | Chr.5:177322159 - 177405557 on Build GRCh38 | Deletion |
F12
LMAN2
SLC34A1
PFN3
RGS14
|
| nsv1161311 | Chr.5:177305104 - 177546474 on Build GRCh38 | Duplication |
GRK6
PDLIM7
F12
PRR7-AS1
SLC34A1
PFN3
RGS14
PRR7
PRELID1
DOK3
FAM193B
LMAN2
MXD3
DDX41
DBN1
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top