Genomic Map
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Target Gene Details
Entrez Gene ID: | 4891 |
Gene Name: | solute carrier family 11 member 2 |
Gene Aliases: |
AHMIO1, DCT1, DMT1, NRAMP2 |
Location: |
Chr.12:50952263-51028335 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC11A2 | NM_001174126.1 | 17 | 1906 | NP_001167597.1 |
| NM_001174127.1 | 17 | 1901 | NP_001167598.1 | |
| NR_033422.1 | ||||
| XM_005268911.3 | 17 | 1958 | XP_005268968.1 | |
| XM_005268912.4 | 16 | 2083 | XP_005268969.1 | |
| XM_011538404.2 | 17 | 2282 | XP_011536706.1 | |
| XM_011538405.2 | 17 | 1890 | XP_011536707.1 | |
| XM_017019355.1 | 17 | 2166 | XP_016874844.1 | |
| XM_017019356.1 | 17 | 2096 | XP_016874845.1 | |
| AB062284.1 | 17 | 1823 | BAB93467.1 | |
| AF064484.1 | 17 | 1849 | AAC21459.1 | |
| AK128640.1 | 17 | 1880 | ||
| CD365137.1 | ||||
| KT455015.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv34039 | Chr.12:50932919 - 51278127 on Build GRCh38 | Loss |
 CSRNP2
LETMD1
POU6F1
PHBP19
SLC11A2
DAZAP2
HIGD1C
SMAGP
TFCP2
|
| nsv1053466 | Chr.12:50956502 - 50982186 on Build GRCh38 | Loss |
SLC11A2
HIGD1C
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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