Genomic Map
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Target Gene Details
Entrez Gene ID: | 3612 |
Gene Name: | inositol monophosphatase 1 |
Gene Aliases: |
IMP, IMPA |
Location: |
Chr.8:81656916-81686354 on Build GRCh38 |
Assay Gene Location: | Within Exon 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| IMPA1 | NM_001144878.1 | 10 | 2287 | NP_001138350.1 |
| NM_001144879.1 | 8 | 1977 | NP_001138351.1 | |
| NM_005536.3 | 9 | 2086 | NP_005527.1 | |
| AF042729.2 | 9 | 2057 | AAB97468.1 | |
| BC008381.1 | 9 | 2052 | AAH08381.1 | |
| BC009565.1 | 9 | 2056 | AAH09565.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv611607 | Chr.8:81405621 - 81768032 on Build GRCh38 | Gain |
 PMP2
FABP12
FABP4
SLC10A5
IMPA1
CHMP4C
ZFAND1
FABP9
|
| nsv831369 | Chr.8:81605833 - 81823586 on Build GRCh38 | Gain+Loss |
SNX16
SLC10A5
IMPA1
CHMP4C
ZFAND1
|
| nsv831368 | Chr.8:81554926 - 81697395 on Build GRCh38 | Gain |
FABP12
SLC10A5
IMPA1
|
| esv2737230 | Chr.8:81633446 - 81689714 on Build GRCh38 | Deletion |
IMPA1
|
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Additional Information:
For this assay, SNP(s) [rs75293486] 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
|
Panther Classification:
Gene Ontology Categories:
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