Genomic Map
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Target Gene Details
Entrez Gene ID: | 55022 |
Gene Name: | phosphotyrosine interaction domain containing 1 |
Gene Aliases: |
HMFN2073, NYGGF4, P-CLI1, PCLI1 |
Location: |
Chr.2:229023973-229271341 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PID1 | NM_001100818.1 | NP_001094288.1 | ||
| NM_017933.4 | NP_060403.3 | |||
| XM_011511384.2 | XP_011509686.1 | |||
| XM_017004404.1 | XP_016859893.1 | |||
| XM_017004405.1 | XP_016859894.1 | |||
| XM_017004406.1 | XP_016859895.1 | |||
| XM_017004407.1 | XP_016859896.1 | |||
| AB075874.1 | BAD38656.1 | |||
| AK000708.1 | BAA91333.1 | |||
| AK096636.1 | ||||
| AK125359.1 | BAC86145.1 | |||
| AY317148.1 | AAP79437.1 | |||
| BC040164.1 | AAH40164.1 | |||
| DB474424.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834563 | Chr.2:228864427 - 229064544 on Build GRCh38 | Gain |
 PID1
|
| nsv3196 | Chr.2:229039146 - 229069883 on Build GRCh38 | Insertion |
PID1
|
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Additional Information:
For this assay, SNP(s) [rs77340890] 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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