SRGAP1
SLIT-ROBO Rho GTPase-activating protein 1
Also known as: ARHGAP13, KIAA1304, SRGP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z6B7
- Gene
- SRGAP1
- Ensembl
- ENSG00000196935
- Chromosome
- 12
- Canonical length
- 1085 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Centrosome,Basal body,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a GTPase activator, working with the GTPase CDC42 to negatively regulate neuronal migration. The encoded protein interacts with the transmembrane receptor ROBO1 to inactivate CDC42. [provided by RefSeq, Sep 2016]
Canonical amino-acid sequenceUniProt
1085 residues, UniProt reviewed canonical sequence.
>Q7Z6B7|SRGAP1
1 MSTPSRFKKD KEIIAEYESQ VKEIRAQLVE QQKCLEQQTE MRVQLLQDLQ DFFRKKAEIE
61 TEYSRNLEKL AERFMAKTRS TKDHQQYKKD QNLLSPVNCW YLLLNQVRRE SKDHATLSDI
121 YLNNVIMRFM QISEDSTRMF KKSKEIAFQL HEDLMKVLNE LYTVMKTYHM YHAESISAES
181 KLKEAEKQEE KQIGRSGDPV FHIRLEERHQ RRSSVKKIEK MKEKRQAKYS ENKLKSIKAR
241 NEYLLTLEAT NASVFKYYIH DLSDLIDCCD LGYHASLNRA LRTYLSAEYN LETSRHEGLD
301 IIENAVDNLE PRSDKQRFME MYPAAFCPPM KFEFQSHMGD EVCQVSAQQP VQAELMLRYQ
361 QLQSRLATLK IENEEVKKTT EATLQTIQDM VTIEDYDVSE CFQHSRSTES VKSTVSETYL
421 SKPSIAKRRA NQQETEQFYF MKLREYLEGS NLITKLQAKH DLLQRTLGEG HRAEYMTTRP
481 PNVPPKPQKH RKSRPRSQYN TKLFNGDLET FVKDSGQVIP LIVESCIRFI NLYGLQHQGI
541 FRVSGSQVEV NDIKNSFERG ENPLADDQSN HDINSVAGVL KLYFRGLENP LFPKERFNDL
601 ISCIRIDNLY ERALHIRKLL LTLPRSVLIV MRYLFAFLNH LSQYSDENMM DPYNLAICFG
661 PTLMPVPEIQ DQVSCQAHVN EIIKTIIIHH ETIFPDAKEL DGPVYEKCMA GDDYCDSPYS
721 EHGTLEEVDQ DAGTEPHTSE DECEPIEAIA KFDYVGRSAR ELSFKKGASL LLYHRASEDW
781 WEGRHNGIDG LVPHQYIVVQ DMDDTFSDTL SQKADSEASS GPVTEDKSSS KDMNSPTDRH
841 PDGYLARQRK RGEPPPPVRR PGRTSDGHCP LHPPHALSNS SVDLGSPSLA SHPRGLLQNR
901 GLNNDSPERR RRPGHGSLTN ISRHDSLKKI DSPPIRRSTS SGQYTGFNDH KPLDPETIAQ
961 DIEETMNTAL NELRELERQS TAKHAPDVVL DTLEQVKNSP TPATSTESLS PLHNVALRSS
1021 EPQIRRSTSS SSDTMSTFKP MVAPRMGVQL KPPALRPKPA VLPKTNPTIG PAPPPQGPTD
1081 KSCTMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SRGAP1 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)
- 0.46
- Highest tissue expression
- 5.9 nTPM
Expression across tissuesHPA
Tissue
- lung: 5.9 nTPM
- parathyroid gland: 5.5 nTPM
- retina: 5.1 nTPM
- ovary: 4.5 nTPM
- pancreas: 4.5 nTPM
- endometrium: 4.1 nTPM
Single-cell type
- podocytes: 1,388 nCPM
- bergmann glia: 633 nCPM
- macrophages: 497 nCPM
- salivary acinar cells: 468 nCPM
- microglia: 412 nCPM
- monocytes: 404 nCPM
Immune cell
- basophil: 0.3 nTPM
- neutrophil: 0.3 nTPM
- intermediate monocyte: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
- memory B-cell: 0.1 nTPM
Brain region
- medulla oblongata: 29 nTPM
- midbrain: 29 nTPM
- thalamus: 26 nTPM
- basal ganglia: 22 nTPM
- cerebellum: 21 nTPM
- hypothalamus: 21 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SRGAP1.
Disease | AllUniProt
Conditions SRGAP1 is implicated in, by any mechanism.
- Thyroid cancer, non-medullary, 2 (NMTC2) MIM:188470
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 181 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.27
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.21
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell migration
- negative regulation of cell migration
- nervous system development
- regulation of synapse assembly
- Rho protein signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Rho GTPase-activating protein domain
- FCH domain
- SH3 domain
- Rho GTPase activation protein
- AH/BAR domain superfamily
- F-BAR domain
- srGAP1/2/3, SH3 domain
- SH3-like domain superfamily
- SLIT-ROBO Rho GTPase-activating
- SH3 domain
- Fes/CIP4, and EFC/F-BAR homology domain
- RhoGAP domain
- SLIT-ROBO Rho GTPase-activating protein 1, F-BAR domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SRGAP1 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 SRGAP1 as an antibody target. Whether an autoantibody or antibody against SRGAP1 could matter depends on whether native SRGAP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SRGAP1 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 SRGAP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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