Assay Details
Target Gene Details
Entrez Gene ID: | 285 |
Gene Name: | angiopoietin 2 |
Gene Aliases: |
AGPT2, ANG2 |
Location: |
Chr.8:6499651-6563420 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ANGPT2 | NM_001118887.1 | 3 | 826 | NP_001112359.1 |
NM_001118888.1 | 2 | 670 | NP_001112360.1 | |
NM_001147.2 | 3 | 826 | NP_001138.1 | |
XM_017013318.1 | 2 | 827 | XP_016868807.1 | |
AB009865.1 | 3 | 525 | BAA95590.1 | |
AF004327.1 | 3 | 846 | AAB63190.1 | |
AF187858.1 | 2 | 361 | AAF76526.1 | |
AF218015.1 | 3 | 579 | AAG17257.1 | |
AK075219.1 | 3 | 808 | ||
AK225698.1 | 3 | 808 | ||
AK290070.1 | 3 | 808 | ||
AK310171.1 | 3 | 808 | ||
AK312541.1 | 3 | 808 | ||
BC126200.1 | 3 | 554 | ||
BC126202.1 | 3 | 554 | ||
BC143902.1 | 3 | 554 |
Target Gene Details
Entrez Gene ID: | 79648 |
Gene Name: | microcephalin 1 |
Gene Aliases: |
BRIT1, MCT |
Location: |
Chr.8:6406592-6648505 on Build GRCh38 |
Assay Gene Location: | Within Intron 14 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MCPH1 | NM_001322042.1 | NP_001308971.1 | ||
NM_024596.4 | NP_078872.2 | |||
XM_011534755.2 | XP_011533057.1 | |||
XM_011534756.2 | XP_011533058.1 | |||
XM_011534757.2 | XP_011533059.1 | |||
XM_011534759.2 | XP_011533061.1 | |||
XM_011534760.2 | XP_011533062.1 | |||
XM_017013829.1 | XP_016869318.1 | |||
XM_017013830.1 | XP_016869319.1 | |||
XM_017013831.1 | XP_016869320.1 | |||
XM_017013832.1 | XP_016869321.1 | |||
XM_017013833.1 | XP_016869322.1 | |||
XM_017013834.1 | XP_016869323.1 | |||
AI480294.1 | ||||
AK022909.1 | BAB14304.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1021684 | Chr.8:6492570 - 6951933 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
dgv2029e212 | Chr.8:6527035 - 6530695 on Build GRCh38 | Loss |
![]() ![]() |
esv2422383 | Chr.8:6504868 - 6924071 on Build GRCh38 | Duplication |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv1022895 | Chr.8:6497692 - 6557353 on Build GRCh38 | Loss |
![]() ![]() |
esv3891314 | Chr.8:6508098 - 6604281 on Build GRCh38 | Gain |
![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs115556798] 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: |
![]() ![]() ![]() ![]() ![]() |
Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)