Assay Details
Target Gene Details
Entrez Gene ID: | 81888 |
Gene Name: | hydroxypyruvate isomerase (putative) |
Gene Aliases: |
HT036 |
Location: |
Chr.1:43450607-43454241 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 8 - Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HYI | NM_001190880.2 | NP_001177809.1 | ||
| NM_001243526.1 | NP_001230455.1 | |||
| NM_031207.5 | NP_112484.3 | |||
| XM_005271239.4 | XP_005271296.1 | |||
| XM_005271240.4 | XP_005271297.1 | |||
| XM_006710937.3 | XP_006711000.1 | |||
| XM_011542222.2 | XP_011540524.1 | |||
| AF284750.1 | AAG59852.1 | |||
| AF284751.1 | AAG59853.1 | |||
| AI023272.1 | ||||
| AK096244.1 | ||||
| AY037165.1 | AAK67642.1 | |||
| AY775560.1 | AAV84474.1 | |||
| BC006140.1 | AAH06140.1 | |||
| BC019041.2 | AAH19041.1 | |||
| CA433653.1 | 1 | 296 | ||
| CD672533.1 | ||||
| JF911821.1 |
Target Gene Details
Entrez Gene ID: | 23334 |
Gene Name: | seizure threshold 2 homolog (mouse) |
Gene Aliases: |
C1orf84, EIEE18, KIAA0467, SZT2A, SZT2B |
Location: |
Chr.1:43389884-43454247 on Build GRCh38 |
Assay Gene Location: | Within Exon 75 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SZT2 | NM_015284.3 | 71 | 11162 | NP_056099.3 |
| AB007936.2 | 57 | 9014 | BAA32312.2 | |
| AK126972.1 | 10 | 3064 | BAC86771.1 | |
| BC151232.1 | 57 | 9014 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv527798 | Chr.1:43446919 - 43451738 on Build GRCh38 | Loss |
|
| nsv546128 | Chr.1:43301467 - 43451738 on Build GRCh38 | Loss |
|
| nsv950701 | Chr.1:43418430 - 43453929 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79439514] 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: |
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Genomic Map