Assay Details
Target Gene Details
Entrez Gene ID: | 80333 |
Gene Name: | potassium voltage-gated channel interacting protein 4 |
Gene Aliases: |
CALP, KCHIP4 |
Location: |
Chr.4:20728520-21948801 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KCNIP4 | NM_001035003.1 | NP_001030175.1 | ||
| NM_025221.5 | NP_079497.2 | |||
| NM_147181.3 | NP_671710.1 | |||
| NM_147182.3 | NP_671711.1 | |||
| XM_011513882.2 | XP_011512184.1 | |||
| XM_011513885.2 | XP_011512187.1 | |||
| XM_011513886.2 | XP_011512188.1 | |||
| AK289661.1 | ||||
| AK289922.1 | ||||
| AY029176.1 | AAK31594.1 | |||
| BX648990.1 | ||||
| DQ148490.1 | AAZ77807.1 |
Target Gene Details
Entrez Gene ID: | 105374516 |
Gene Name: | uncharacterized LOC105374516 |
Gene Aliases: |
- |
Location: |
Chr.4:21582096-21613722 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC105374516 | NR_134233.1 | |||
| CR743425.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv4268 | Chr.4:21574983 - 21598037 on Build GRCh38 | Insertion |
|
| nsv461289 | Chr.4:21586675 - 21637893 on Build GRCh38 | Gain |
|
| dgv5154n100 | Chr.4:21578800 - 21638727 on Build GRCh38 | Gain |
|
| nsv829879 | Chr.4:21416945 - 21609379 on Build GRCh38 | Gain |
|
| nsv1013365 | Chr.4:20832431 - 21607455 on Build GRCh38 | Gain |
|
| esv3599877 | Chr.4:21557212 - 21695003 on Build GRCh38 | Loss |
|
| esv3599878 | Chr.4:21557332 - 21651050 on Build GRCh38 | Loss |
|
| nsv829880 | Chr.4:21490803 - 21692193 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73254304] 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: |
|

Genomic Map