Genomic Map
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Target Gene Details
Entrez Gene ID: | 10672 |
Gene Name: | G protein subunit alpha 13 |
Gene Aliases: |
G13 |
Location: |
Chr.17:65009289-65056802 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GNA13 | NM_001282425.1 | NP_001269354.1 | ||
| NM_006572.5 | NP_006563.2 | |||
| AF493902.1 | AAM12616.1 | |||
| AK301699.1 | ||||
| AK302400.1 | ||||
| AK313672.1 | ||||
| BC036756.1 | AAH36756.1 | |||
| L22075.1 | AAA74235.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1066765 | Chr.17:64520760 - 65128185 on Build GRCh38 | Gain |
 MIR4315-2
CEP95
MIR6080
GNA13
LRRC37A3
LOC146880
PLEKHM1P1
AMZ2P1
SMURF2
LOC100507002
|
| nsv952361 | Chr.17:65009183 - 65052982 on Build GRCh38 | Duplication |
GNA13
|
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Additional Information:
For this assay, SNP(s) [rs114576022] 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
|
Panther Classification:
Gene Ontology Categories:
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