SRGAP2
SLIT-ROBO Rho GTPase-activating protein 2
Also known as: ARHGAP34, FNBP2, KIAA0456, SRGAP2A, SRGP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75044
- Gene
- SRGAP2
- Ensembl
- ENSG00000266028
- Chromosome
- 1
- Canonical length
- 1071 aa
- Protein class
- Disease related genes, Predicted intracellular proteins
- Subcellular location
- Centrosome,Basal body,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This locus encodes a member of the SLIT-ROBO Rho GTPase activating protein family. The encoded protein stimulates GTPase activity of Rac1, and plays a role in cortical neuron development. This locus has several paralogs on human chromosome 1 resulting from segmental duplication. While this locus itself is conserved among various species, the paralogs are found only in the genus Homo, and not in the genomes of non-human great apes. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Jul 2014]
Canonical amino-acid sequenceUniProt
1071 residues, UniProt reviewed canonical sequence.
>O75044|SRGAP2
1 MTSPAKFKKD KEIIAEYDTQ VKEIRAQLTE QMKCLDQQCE LRVQLLQDLQ DFFRKKAEIE
61 MDYSRNLEKL AERFLAKTRS TKDQQFKKDQ NVLSPVNCWN LLLNQVKRES RDHTTLSDIY
121 LNNIIPRFVQ VSEDSGRLFK KSKEVGQQLQ DDLMKVLNEL YSVMKTYHMY NADSISAQSK
181 LKEAEKQEEK QIGKSVKQED RQTPRSPDST ANVRIEEKHV RRSSVKKIEK MKEKRQAKYT
241 ENKLKAIKAR NEYLLALEAT NASVFKYYIH DLSDLIDQCC DLGYHASLNR ALRTFLSAEL
301 NLEQSKHEGL DAIENAVENL DATSDKQRLM EMYNNVFCPP MKFEFQPHMG DMASQLCAQQ
361 PVQSELVQRC QQLQSRLSTL KIENEEVKKT MEATLQTIQD IVTVEDFDVS DCFQYSNSME
421 SVKSTVSETF MSKPSIAKRR ANQQETEQFY FTKMKEYLEG RNLITKLQAK HDLLQKTLGE
481 SQRTDCSLAR RSSTVRKQDS SQAIPLVVES CIRFISRHGL QHEGIFRVSG SQVEVNDIKN
541 AFERGEDPLA GDQNDHDMDS IAGVLKLYFR GLEHPLFPKD IFHDLMACVT MDNLQERALH
601 IRKVLLVLPK TTLIIMRYLF AFLNHLSQFS EENMMDPYNL AICFGPSLMS VPEGHDQVSC
661 QAHVNELIKT IIIQHENIFP SPRELEGPVY SRGGSMEDYC DSPHGETTSV EDSTQDVTAE
721 HHTSDDECEP IEAIAKFDYV GRTARELSFK KGASLLLYQR ASDDWWEGRH NGIDGLIPHQ
781 YIVVQDTEDG VVERSSPKSE IEVISEPPEE KVTARAGASC PSGGHVADIY LANINKQRKR
841 PESGSIRKTF RSDSHGLSSS LTDSSSPGVG ASCRPSSQPI MSQSLPKEGP DKCSISGHGS
901 LNSISRHSSL KNRLDSPQIR KTATAGRSKS FNNHRPMDPE VIAQDIEATM NSALNELREL
961 ERQSSVKHTP DVVLDTLEPL KTSPVVAPTS EPSSPLHTQL LKDPEPAFQR SASTAGDIAC
1021 AFRPVKSVKM AAPVKPPATR PKPTVFPKTN ATSPGVNSST SPQSTDKSCT VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SRGAP2 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
- 0
- Mean surface accessibility (rSASA)
- 0.45
- Highest tissue expression
- 123 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 123 nTPM
- skin: 40 nTPM
- spinal cord: 27 nTPM
- parathyroid gland: 23 nTPM
- spleen: 22 nTPM
- cerebral cortex: 21 nTPM
Single-cell type
- microglia: 2,480 nCPM
- podocytes: 1,255 nCPM
- macrophages: 323 nCPM
- brain excitatory neurons: 273 nCPM
- cdc: 211 nCPM
- monocytes: 208 nCPM
Immune cell
- non-classical monocyte: 10 nTPM
- intermediate monocyte: 8.6 nTPM
- plasmacytoid DC: 8.4 nTPM
- classical monocyte: 6.7 nTPM
- myeloid DC: 6.1 nTPM
- neutrophil: 5.9 nTPM
Brain region
- cerebellum: 196 nTPM
- pons: 113 nTPM
- white matter: 108 nTPM
- medulla oblongata: 96 nTPM
- cerebral cortex: 94 nTPM
- spinal cord: 91 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)
- 0.31
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 3.19
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin filament severing
- dendritic spine development
- excitatory synapse assembly
- extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration
- filopodium assembly
- inhibitory synapse assembly
- negative regulation of cell migration
- negative regulation of neuron migration
- nervous system development
- neuron projection morphogenesis
- positive regulation of GTPase activity
- regulation of small GTPase mediated signal transduction
- regulation of synapse assembly
- signal transduction
- substrate adhesion-dependent cell spreading
- lamellipodium assembly involved in ameboidal cell migration
Molecular functions
- GTPase activator activity
- identical protein binding
- protein homodimerization activity
- small GTPase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SRGAP2 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 SRGAP2 as an antibody target. Whether an autoantibody or antibody against SRGAP2 could matter depends on whether native SRGAP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SRGAP2 is annotated at the cell surface, where native SRGAP2 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 SRGAP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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