Genomic Map
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Target Gene Details
Entrez Gene ID: | 9063 |
Gene Name: | protein inhibitor of activated STAT 2 |
Gene Aliases: |
ARIP3, DIP, MIZ, MIZ1, PIASX, PIASX-ALPHA, PIASX-BETA, SIZ2, ZMIZ4 |
Location: |
Chr.18:46803224-46920167 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PIAS2 | NM_001324046.1 | NP_001310975.1 | ||
| NM_001324047.1 | NP_001310976.1 | |||
| NM_001324048.1 | NP_001310977.1 | |||
| NM_001324049.1 | NP_001310978.1 | |||
| NM_001324051.1 | 14 | 2422 | NP_001310980.1 | |
| NM_001324052.1 | 16 | 2612 | NP_001310981.1 | |
| NM_001324053.1 | 16 | 2771 | NP_001310982.1 | |
| NM_001324054.1 | 14 | 2402 | NP_001310983.1 | |
| NM_004671.4 | NP_004662.2 | |||
| NM_173206.3 | 13 | 2313 | NP_775298.1 | |
| NR_136684.1 | ||||
| NR_136685.1 | 12 | 1838 | ||
| XM_005258377.3 | XP_005258434.1 | |||
| XM_005258379.3 | XP_005258436.1 | |||
| XM_006722571.3 | XP_006722634.1 | |||
| XM_006722572.3 | XP_006722635.1 | |||
| XM_006722573.2 | 14 | 2296 | XP_006722636.1 | |
| XM_011526258.2 | XP_011524560.1 | |||
| XM_011526259.2 | XP_011524561.1 | |||
| XM_017026068.1 | XP_016881557.1 | |||
| XM_017026069.1 | XP_016881558.1 | |||
| XM_017026070.1 | XP_016881559.1 | |||
| XM_017026071.1 | 14 | 2227 | XP_016881560.1 | |
| AF077954.1 | AAC36705.1 | |||
| AK308143.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428355 | Chr.18:46580218 - 46826322 on Build GRCh38 | Gain |
 ST8SIA5
PIAS2
LOXHD1
|
| nsv9629 | Chr.18:46684730 - 47231140 on Build GRCh38 | Gain+Loss |
KATNAL2
HDHD2
ST8SIA5
PIAS2
TCEB3C
SKOR2
LOC107983955
TCEB3CL
TCEB3CL2
IER3IP1
TCEB3B
|
| dgv614e214 | Chr.18:46702717 - 46833888 on Build GRCh38 | Gain |
ST8SIA5
PIAS2
|
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Additional Information:
For this assay, SNP(s) [rs72907112] 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
Exonic
DGV Variation
|
Gene Ontology Categories:
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