SIRPG
Signal-regulatory protein gamma
Also known as: bA77C3.1, CD172g, SIRP-B2, SIRPB2, SIRPG_HUMAN, SIRPgamma
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P1W8
- Gene
- SIRPG
- Ensembl
- ENSG00000089012
- Chromosome
- 20
- Canonical length
- 387 aa
- Protein class
- CD markers, Predicted membrane proteins
OverviewNCBI Gene
The protein encoded by this gene is a member of the signal-regulatory protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
387 residues, UniProt reviewed canonical sequence.
>Q9P1W8|SIRPG
1 MPVPASWPHP PGPFLLLTLL LGLTEVAGEE ELQMIQPEKL LLVTVGKTAT LHCTVTSLLP
61 VGPVLWFRGV GPGRELIYNQ KEGHFPRVTT VSDLTKRNNM DFSIRISSIT PADVGTYYCV
121 KFRKGSPENV EFKSGPGTEM ALGAKPSAPV VLGPAARTTP EHTVSFTCES HGFSPRDITL
181 KWFKNGNELS DFQTNVDPTG QSVAYSIRST ARVVLDPWDV RSQVICEVAH VTLQGDPLRG
241 TANLSEAIRV PPTLEVTQQP MRVGNQVNVT CQVRKFYPQS LQLTWSENGN VCQRETASTL
301 TENKDGTYNW TSWFLVNISD QRDDVVLTCQ VKHDGQLAVS KRLALEVTVH QKDQSSDATP
361 GPASSLTALL LIAVLLGPIY VPWKQKTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SIRPG 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 36 nTPM
Expression across tissuesHPA
Tissue
- thymus: 36 nTPM
- lymph node: 32 nTPM
- tonsil: 26 nTPM
- appendix: 12 nTPM
- spleen: 8.8 nTPM
- small intestine: 5.3 nTPM
Single-cell type
- late primary spermatocytes: 61 nCPM
- t-cells: 44 nCPM
- early spermatids: 30 nCPM
- late spermatids: 13 nCPM
- nk-cells: 10 nCPM
- melanocytes: 2.7 nCPM
Immune cell
- T-reg: 370 nTPM
- naive CD4 T-cell: 217 nTPM
- memory CD4 T-cell: 208 nTPM
- MAIT T-cell: 187 nTPM
- naive CD8 T-cell: 177 nTPM
- memory CD8 T-cell: 158 nTPM
Brain region
- cerebral cortex: 0.5 nTPM
- white matter: 0.5 nTPM
- medulla oblongata: 0.4 nTPM
- basal ganglia: 0.2 nTPM
- pons: 0.2 nTPM
- spinal cord: 0.2 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)
- 1.75
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.27
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell adhesion
- cell-cell signaling
- intracellular signal transduction
- negative regulation of cell population proliferation
- positive regulation of cell population proliferation
- positive regulation of cell-cell adhesion
- positive regulation of phagocytosis
- positive regulation of T cell activation
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SIRPG in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SIRPG as an antibody target. Whether an autoantibody or antibody against SIRPG could matter depends on whether native SIRPG is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SIRPG is annotated at the cell surface, where native SIRPG is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SIRPG as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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