Genomic Map
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Target Gene Details
Entrez Gene ID: | 6556 |
Gene Name: | solute carrier family 11 member 1 |
Gene Aliases: |
LSH, NRAMP, NRAMP1 |
Location: |
Chr.2:218381766-218396894 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC11A1 | NM_000578.3 | 1 | 122 | NP_000569.3 |
| XM_005246793.3 | 1 | 385 | XP_005246850.1 | |
| XM_005246794.3 | 1 | 385 | XP_005246851.1 | |
| XM_006712709.3 | 1 | 385 | XP_006712772.1 | |
| XM_006712710.3 | 1 | 385 | XP_006712773.1 | |
| XM_006712711.3 | 1 | 385 | XP_006712774.1 | |
| XM_011511684.2 | 1 | 385 | XP_011509986.1 | |
| XM_011511685.2 | 1 | 385 | XP_011509987.1 | |
| XM_017004765.1 | 1 | 385 | XP_016860254.1 | |
| XM_017004766.1 | 1 | 385 | XP_016860255.1 | |
| AK307954.1 | 1 | 122 | ||
| D50402.1 | BAA08907.1 | |||
| DB284801.1 | 1 | 122 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv519829 | Chr.2:218286495 - 218403058 on Build GRCh38 | Loss |
 MIR26B
PNKD
MIR6810
CATIP-AS2
TMBIM1
CATIP-AS1
CATIP
CTDSP1
SLC11A1
|
| nsv3166 | Chr.2:218371765 - 218405183 on Build GRCh38 | Insertion |
MIR26B
CTDSP1
SLC11A1
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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