TAGAP
T-cell activation Rho GTPase-activating protein
Also known as: ARHGAP47, FLJ32631, IDDM21, TAGAP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N103
- Gene
- TAGAP
- Ensembl
- ENSG00000164691
- Chromosome
- 6
- Canonical length
- 731 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a member of the Rho GTPase-activator protein superfamily. The encoded protein may function as a Rho GTPase-activating protein. Alterations in this gene may be associated with several diseases, including rheumatoid arthritis, celiac disease, and multiple sclerosis. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013]
Canonical amino-acid sequenceUniProt
731 residues, UniProt reviewed canonical sequence.
>Q8N103|TAGAP
1 MKLRSSHNAS KTLNANNMET LIECQSEGDI KEHPLLASCE SEDSICQLIE VKKRKKVLSW
61 PFLMRRLSPA SDFSGALETD LKASLFDQPL SIICGDSDTL PRPIQDILTI LCLKGPSTEG
121 IFRRAANEKA RKELKEELNS GDAVDLERLP VHLLAVVFKD FLRSIPRKLL SSDLFEEWMG
181 ALEMQDEEDR IEALKQVADK LPRPNLLLLK HLVYVLHLIS KNSEVNRMDS SNLAICIGPN
241 MLTLENDQSL SFEAQKDLNN KVKTLVEFLI DNCFEIFGEN IPVHSSITSD DSLEHTDSSD
301 VSTLQNDSAY DSNDPDVESN SSSGISSPSR QPQVPMATAA GLDSAGPQDA REVSPEPIVS
361 TVARLKSSLA QPDRRYSEPS MPSSQECLES RVTNQTLTKS EGDFPVPRVG SRLESEEAED
421 PFPEEVFPAV QGKTKRPVDL KIKNLAPGSV LPRALVLKAF SSSSLDASSD SSPVASPSSP
481 KRNFFSRHQS FTTKTEKGKP SREIKKHSMS FTFAPHKKVL TKNLSAGSGK SQDFTRDHVP
541 RGVRKESQLA GRIVQENGCE THNQTARGFC LRPHALSVDD VFQGADWERP GSPPSYEEAM
601 QGPAARLVAS ESQTVGSMTV GSMRARMLEA HCLLPPLPPA HHVEDSRHRG SKEPLPGHGL
661 SPLPERWKQS RTVHASGDSL GHVSGPGRPE LLPLRTVSES VQRNKRDCLV RRCSQPVFEA
721 DQFQYAKESY ILocalizationUniProt · AlphaFold · HPA
Whether an antibody against TAGAP can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.59
- Highest tissue expression
- 139 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 139 nTPM
- tonsil: 45 nTPM
- lymph node: 37 nTPM
- appendix: 27 nTPM
- smooth muscle: 24 nTPM
- thymus: 23 nTPM
Single-cell type
- neutrophils: 837 nCPM
- neutrophil progenitors: 162 nCPM
- t-cells: 150 nCPM
- b-cells: 134 nCPM
- nk-cells: 125 nCPM
- plasma cells: 120 nCPM
Immune cell
- neutrophil: 170 nTPM
- basophil: 164 nTPM
- eosinophil: 89 nTPM
- memory CD4 T-cell: 74 nTPM
- memory CD8 T-cell: 65 nTPM
- MAIT T-cell: 63 nTPM
Brain region
- white matter: 13 nTPM
- hypothalamus: 11 nTPM
- choroid plexus: 9.9 nTPM
- medulla oblongata: 9.4 nTPM
- spinal cord: 8.4 nTPM
- thalamus: 8.3 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.42
- gnomAD pLI
- 0.85
- gnomAD missense Z
- 1.4
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 1% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- regulation of Rho protein signal transduction
- regulation of small GTPase mediated signal transduction
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TAGAP as an antibody target. Whether an autoantibody or antibody against TAGAP could matter depends on whether native TAGAP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TAGAP is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TAGAP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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