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 | 2849 | NP_001167597.1 |
| NM_001174127.1 | 17 | 2844 | NP_001167598.1 | |
| NR_033422.1 | ||||
| XM_005268911.3 | 17 | 2901 | XP_005268968.1 | |
| XM_005268912.4 | 16 | 3026 | XP_005268969.1 | |
| XM_011538404.2 | 17 | 3225 | XP_011536706.1 | |
| XM_011538405.2 | 17 | 2833 | XP_011536707.1 | |
| XM_017019355.1 | 17 | 3109 | XP_016874844.1 | |
| XM_017019356.1 | 17 | 3039 | XP_016874845.1 | |
| AF064484.1 | 17 | 2792 | AAC21459.1 | |
| AK128640.1 | 17 | 2823 | ||
| CD365137.1 |
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 |
 SMAGP
HIGD1C
CSRNP2
TFCP2
POU6F1
LETMD1
SLC11A2
PHBP19
DAZAP2
|
| nsv1053466 | Chr.12:50956502 - 50982186 on Build GRCh38 | Loss |
HIGD1C
SLC11A2
|
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Additional Information:
For this assay, SNP(s) [rs77801666] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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