GENE REFERENCE / HGNC:12858
ZAP70
zeta chain of T cell receptor associated protein kinase 70
What does this gene do?
The ZAP70 gene provides instructions for making a protein called zeta-chain-associated protein kinase. This protein is part of a signaling pathway that directs the development of and turns on (activates) immune system cells called T cells. T cells identify foreign substances and defend the body against infection.
The ZAP70 gene is important for the development and function of several types of T cells. These include cytotoxic T cells (CD8+ T cells), whose functions include destroying cells infected by viruses. The ZAP70 gene is also involved in the activation of helper T cells (CD4+ T cells). These cells direct and assist the functions of the immune system by influencing the activities of other immune system cells.
Related condition topics
MedlinePlus mentions this gene in the condition pages below. These links alone do not show that the gene causes a condition.
ClinGen reviews
ClinGen reviews the evidence linking a particular gene to a condition. Each rating below describes the strength of that link. It does not classify a variant in your DNA file.
| Condition | Inheritance | Evidence |
|---|---|---|
| combined immunodeficiency due to ZAP70 deficiencyMONDO:0010023 · Evaluated 2022-02-08 | Autosomal recessive | DefinitiveSCID-CID Gene Curation Expert Panel |
ClinVar records
These numbers show what has been submitted to ClinVar. They cannot tell you how likely you are to have a condition.
- Submitted alleles
- 615
- Submissions for variants in or overlapping this gene
- 924
- Submissions explicitly reporting this gene
- 882
- Alleles reported pathogenic / likely pathogenic
- 38
- VariationIDs with uncertain significance
- 229
- VariationIDs with conflicting classifications
- 23
The rows count different things: alleles, submissions or VariationIDs. Their categories can overlap, so do not add them together. Pathogenic/likely pathogenic counts exclude structural variants that merely overlap a gene. A dash in the source means “not reported,” not zero.
NCBI produces the gene-summary file each week using counts recorded at the start of the month. The numbers may differ from those on the live ClinVar website. Read the field definitions ↗
YOUR DNA FILE
Can your DNA file tell you about ZAP70?
From a DNA test kit (such as 23andMe, AncestryDNA or MyHeritage). These kits check a fixed list of about 600,000 to 700,000 positions across your whole genome. ClinVar lists 38 alleles in ZAP70 reported as pathogenic or likely pathogenic. A kit checks only some of these positions, and often none of them.
From whole genome sequencing (a VCF file). Sequencing reads most of your genome. Your file lists the places where your DNA differs from the reference genome. Some regions are hard to sequence, including parts of some genes that have near-identical copies elsewhere, and a VCF file does not record which positions were read well.
If a variant is not in your file, that does not mean you don’t have it.
What BioDecode checks
BioDecode compares every variant in your file with ClinVar, on your own computer. For each match, it shows the ClinVar classification, the review status and the condition it was reported for. Your file is not uploaded.
A ClinVar classification applies to one particular variant and the condition it was reported for. It does not tell you about other variants in ZAP70.
BioDecode cannot fill gaps in your test, diagnose a condition or replace clinical testing.
Sources and dates
The source information on this page last changed on 2026-10-10.
HGNC Source details
Source release: Fri, 09 Oct 2026 13:40:45 GMT
Source record updated: 2023-01-20
SHA-256: e4cd9c6d7120051b80e5e61d2aeb98bd6a541ddd21f428a6eab922c11242e053
MedlinePlus Source details
Source release: Sat, 10 Oct 2026 05:16:07 GMT
Source publication: 2020-08-18
Source review: 2009-11
SHA-256: fdc8bd614310c12718379cef6569962e5d0e791cecabcc355b53a72816ac263a
ClinVar Source details
Source release: Sun, 04 Oct 2026 13:15:29 GMT
SHA-256: 126d9e5bded1d43c0380ac6684c86f9aab056d2ff2be93d743e408ed917ae558
ClinGen Source details
Source release: Sat, 10 Oct 2026 09:49:14 GMT
SHA-256: 5bbc9404c72cc21d80e36ea4c49380231755850af5c34064262adceb74881af6
About the library sources · Latest validated release · Record cd0eb6ab7de4