Assay Details
Target Gene Details
Entrez Gene ID: | 3084 |
Gene Name: | neuregulin 1 |
Gene Aliases: |
ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF, NRG1-IT2, SMDF |
Location: |
Chr.8:31639222-32771716 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NRG1 | NM_001159995.2 | NP_001153467.1 | ||
NM_001159999.2 | NP_001153471.1 | |||
NM_001160001.2 | NP_001153473.1 | |||
NM_001322201.1 | NP_001309130.1 | |||
NM_001322202.1 | NP_001309131.1 | |||
NM_013962.2 | NP_039256.2 | |||
XM_011544512.2 | XP_011542814.1 | |||
XM_017013365.1 | XP_016868854.1 | |||
XM_017013366.1 | XP_016868855.1 | |||
XM_017013367.1 | XP_016868856.1 | |||
XM_017013371.1 | XP_016868860.1 | |||
XM_017013372.1 | XP_016868861.1 | |||
CN603652.1 | ||||
CN603654.1 | ||||
EF372273.1 | ||||
EF372274.1 | ||||
EF372275.1 | ||||
EF372276.1 | ||||
EF372277.1 | ||||
EF517295.1 | ||||
EF517296.1 | ||||
EF517297.1 | ||||
GQ983557.1 | ||||
GQ983558.1 | ||||
L12260.1 | AAB59622.1 |
Target Gene Details
Entrez Gene ID: | 100856811 |
Gene Name: | NRG1 intronic transcript 1 |
Gene Aliases: |
- |
Location: |
Chr.8:32025736-32139477 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NRG1-IT1 | NR_104156.1 | |||
NR_104157.1 | ||||
NR_104158.1 | ||||
AA394309.1 | ||||
HY002956.1 | ||||
HY047999.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831282 | Chr.8:31914080 - 32084948 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs75968202,rs77906903] 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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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)