Genomic Map
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Target Gene Details
Entrez Gene ID: | 9232 |
Gene Name: | pituitary tumor-transforming 1 |
Gene Aliases: |
EAP1, HPTTG, PTTG, TUTR1 |
Location: |
Chr.5:160421807-160428744 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PTTG1 | NM_001282382.1 | NP_001269311.1 | ||
| NM_001282383.1 | NP_001269312.1 | |||
| NM_004219.3 | NP_004210.1 | |||
| AF062649.1 | AAC69752.1 | |||
| AF075242.1 | AAD19335.1 | |||
| AF095287.1 | AAC64409.1 | |||
| AJ223953.1 | CAA11683.1 | |||
| AK312209.1 | ||||
| BC101834.1 | AAI01835.1 | |||
| BC108894.1 | AAI08895.1 | |||
| BC108895.1 | AAI08896.1 | |||
| BC112071.1 | AAI12072.1 | |||
| BC113842.1 | AAI13843.1 | |||
| BC113896.1 | AAI13897.1 | |||
| BC128193.1 | ||||
| BC128194.1 | ||||
| BM990391.1 | ||||
| BU182149.1 | ||||
| CR457135.1 | CAG33416.1 | |||
| CR541685.1 | CAG46486.1 | |||
| HY006026.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1015634 | Chr.5:159750943 - 160620377 on Build GRCh38 | Gain |
 C1QTNF2
TTC1
ZBED8
MIR3142HG
LOC101927766
MIR146A
FABP6
LOC101927790
MIR3142
SLU7
ADRA1B
ATP10B
PWWP2A
CCNJL
PTTG1
|
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Additional Information:
For this assay, SNP(s) [rs73316384] 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
|
Gene Ontology Categories:
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