Assay Details
Target Gene Details
Entrez Gene ID: | 22854 |
Gene Name: | netrin G1 |
Gene Aliases: |
Lmnt1 |
Location: |
Chr.1:107139918-107484899 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NTNG1 | NM_001312688.1 | NP_001299617.1 | ||
NM_014917.3 | NP_055732.2 | |||
XM_006710455.2 | XP_006710518.1 | |||
XM_006710456.3 | XP_006710519.1 | |||
XM_011541021.1 | XP_011539323.1 | |||
XM_011541024.2 | XP_011539326.1 | |||
XM_011541025.1 | XP_011539327.1 | |||
XM_017000680.1 | XP_016856169.1 | |||
XM_017000681.1 | XP_016856170.1 | |||
XM_017000682.1 | XP_016856171.1 | |||
XM_017000683.1 | XP_016856172.1 | |||
XM_017000684.1 | XP_016856173.1 | |||
XM_017000685.1 | XP_016856174.1 | |||
XM_017000686.1 | XP_016856175.1 | |||
AB023193.1 | BAA76820.2 | |||
AK296533.1 | ||||
BC030220.1 | AAH30220.1 | |||
BX538348.1 | CAD98143.1 | |||
DA195069.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2758957 | Chr.1:106941006 - 107298261 on Build GRCh38 | Loss | NTNG1 PRMT6 |
nsv1001678 | Chr.1:107117748 - 107155038 on Build GRCh38 | Loss | NTNG1 |
nsv830982 | Chr.1:107108954 - 107292352 on Build GRCh38 | Gain | NTNG1 |
nsv547330 | Chr.1:107006123 - 107375697 on Build GRCh38 | Gain | NTNG1 PRMT6 |
More Information
Additional Information:
For this assay, SNP(s) [rs76335573] 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 Intronic Non-exonic DGV Variation |