ZAP70

GENERAL INFORMATION

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Gene name

ZAP70

Gene description

Zeta-chain (TCR) associated protein kinase 70kDa

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins
RAS pathway related proteins

Predicted localization

Intracellular

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (lymph node)
GTEx:Group enriched (lung, small intestine, spleen)

Protein evidence

Evidence at protein level

Protein localization

Selective cytoplasmic expression in subsets of lymphoid cells.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA003134 , CAB002625
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (lymph node)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (lung, small intestine, spleen)

Organ

Expression



GENE INFORMATION

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Gene name

ZAP70 (HGNC Symbol)

Synonyms

SRK, STD, ZAP-70

Description

Zeta-chain (TCR) associated protein kinase 70kDa (HGNC Symbol)

Entrez gene summary

This gene encodes an enzyme belonging to the protein tyrosine kinase family, and it plays a role in T-cell development and lymphocyte activation. This enzyme, which is phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation, functions in the initial step of TCR-mediated signal transduction in combination with the Src family kinases, Lck and Fyn. This enzyme is also essential for thymocyte development. Mutations in this gene cause selective T-cell defect, a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells. Two transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Chromosome

2

Cytoband

q11.2

Chromosome location (bp)

97713560 - 97739862

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000115085 (version 78.38)

Entrez gene

7535

UniProt

P43403 (UniProt - Evidence at protein level)

neXtProt

NX_P43403

Antibodypedia

ZAP70 antibodies


PROTEIN BROWSER

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ENST00000264972
 
ENST00000451498
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ZAP70-001 ENSP00000264972
ENST00000264972
P43403
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Show » Show » 619 69.9 No 0
ZAP70-008 ENSP00000400475
ENST00000451498
P43403
Show all »
Show » Show » 312 35.6 No 0