Genomic Map
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Target Gene Details
Entrez Gene ID: | 3702 |
Gene Name: | IL2 inducible T-cell kinase |
Gene Aliases: |
EMT, LPFS1, LYK, PSCTK2 |
Location: |
Chr.5:157180896-157255185 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ITK | NM_005546.3 | NP_005537.3 | ||
| AB209622.1 | BAD92859.1 | |||
| AK303609.1 | ||||
| AK312846.1 | ||||
| BC109077.2 | AAI09078.1 | |||
| BC109078.1 | AAI09079.1 | |||
| D13720.1 | BAA02873.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv1662e212 | Chr.5:157183659 - 157186764 on Build GRCh38 | Gain |
 ITK
|
| esv3575895 | Chr.5:157183660 - 157192169 on Build GRCh38 | Gain |
ITK
|
| esv3575892 | Chr.5:156975204 - 157220778 on Build GRCh38 | Gain |
HAVCR2
MED7
HAVCR1
ITK
FAM71B
|
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Additional Information:
For this assay, SNP(s) [rs76585787] 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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