Assay Details
Target Gene Details
Entrez Gene ID: | 56171 |
Gene Name: | dynein axonemal heavy chain 7 |
Gene Aliases: |
- |
Location: |
Chr.2:195737604-196075188 on Build GRCh38 |
Assay Gene Location: | Within Exon 68 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DNAH7 | NM_018897.2 | NP_061720.2 | ||
| XM_011511487.2 | 66 | 12805 | XP_011509789.1 | |
| XM_011511488.2 | 64 | 13479 | XP_011509790.1 | |
| XM_011511489.2 | 64 | 12391 | XP_011509791.1 | |
| XM_011511490.2 | 64 | 13374 | XP_011509792.1 | |
| XM_011511497.2 | 32 | 6825 | XP_011509799.1 | |
| XM_017004504.1 | 64 | 13325 | XP_016859993.1 | |
| AB023161.2 | ||||
| AF327442.1 | AAL37427.1 | |||
| BC029567.1 | AAH29567.1 | |||
| BX117789.1 |
Target Gene Details
Entrez Gene ID: | 57181 |
Gene Name: | solute carrier family 39 member 10 |
Gene Aliases: |
LZT-Hs2 |
Location: |
Chr.2:195575949-195737702 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 17 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC39A10 | NM_001127257.1 | NP_001120729.1 | ||
| NM_020342.2 | NP_065075.1 | |||
| XM_005246689.4 | XP_005246746.2 | |||
| XM_011511504.2 | XP_011509806.1 | |||
| XM_011511505.2 | XP_011509807.1 | |||
| XM_011511506.2 | XP_011509808.1 | |||
| AB033091.1 | ||||
| AI693720.1 | ||||
| BC073909.1 | AAH73909.1 | |||
| CR749813.1 | CAH18673.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv3094 | Chr.2:195697571 - 195742409 on Build GRCh38 | Deletion |
|
| nsv834501 | Chr.2:195608503 - 195778199 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs200805801] 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: |
|

Genomic Map