Genomic Map
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Target Gene Details
Entrez Gene ID: | 30061 |
Gene Name: | solute carrier family 40 member 1 |
Gene Aliases: |
FPN1, HFE4, IREG1, MST079, MSTP079, MTP1, SLC11A3 |
Location: |
Chr.2:189560590-189580811 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC40A1 | NM_014585.5 | 7 | 1703 | NP_055400.1 |
| XM_005246505.1 | 8 | 1838 | XP_005246562.1 | |
| XM_017003938.1 | 8 | 1952 | XP_016859427.1 | |
| AF215636.1 | 7 | 1656 | AAF80986.1 | |
| AF226614.1 | 7 | 1656 | AAF36697.1 | |
| AF231121.1 | 7 | 1656 | AAF44330.1 | |
| AK002038.1 | 2 | 638 | BAA92049.1 | |
| AK223236.1 | 7 | 1678 | BAD96956.1 | |
| AK292146.1 | 7 | 1678 | ||
| AK314827.1 | 7 | 1678 | ||
| AL136944.1 | 7 | 1666 | CAB66878.1 | |
| BC035893.1 | 7 | 1667 | AAH35893.1 | |
| BC037733.1 | 7 | 1782 | AAH37733.1 | |
| CR533564.1 | 7 | 1352 | CAG38595.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv954448 | Chr.2:189550075 - 189580174 on Build GRCh38 | Duplication |
 SLC40A1
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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