PLEKHG4B
Pleckstrin homology domain-containing family G member 4B
Also known as: KIAA1909, PKH4B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96PX9
- Gene
- PLEKHG4B
- Ensembl
- ENSG00000153404
- Chromosome
- 5
- Canonical length
- 1627 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a large protein that contains a pleckstrin homology domain and may function as a guanine nucleotide exchange factor. [provided by RefSeq, May 2017]
Canonical amino-acid sequenceUniProt
1627 residues, UniProt reviewed canonical sequence.
>Q96PX9|PLEKHG4B
1 MGFSTADGGG GPGARDLESL DACIQRTLSA LYPPFEATAA TVLWQLFSVA ERCHGGDGLH
61 CLTSFLLPAK RALQHLQQEA CARYRGLVFL HPGWPLCAHE KVVVQLASLH GVRLQPGDFY
121 LQVTSAGKQS ARLVLKCLSR LGRGTEEVTV PEAMYGCVFT GAFLEWVNRE RRHVPLQTCL
181 LTSGLAVHRA PWSDVTDPVF VPSPGAILQS YSSCTGPERL PSSPSEAPVP TQATAGPHFQ
241 GSASCPDTLT SPCRRGHTGS DQLRHLPYPE RAELGSPRTL SGSSDRDFEK VSPSEQGPRM
301 PPENCGGSGE RPDPMDQEDR PKALTFHTDL GIPSSRRRPP GDPTCVQPRR WFRESYMEAL
361 RNPMPLGSSE EALGDLACSS LTGASRDLGT GAVASGTQEE TSGPRGDPQQ TPSLEKERHT
421 PSRTGPGAAG RTLPRRSRSW ERAPRSSRGA QAAACHTSHH SAGSRPGGHL GGQAVGTPNC
481 VPVEGPGCTK EEDVLASSAC VSTDGGSLHC HNPSGPSDVP ARQPHPEQEG WPPGTGDFPS
541 QVPKQVLDVS QELLQSGVVT LPGTRDRHGR AVVQVRTRSL LWTREHSSCA ELTRLLLYFH
601 SIPRKEVRDL GLVVLVDARR SPAAPAVSQA LSGLQNNTSP IIHSILLLVD KESAFRPDKD
661 AIIQCEVVSS LKAVHKFVDS CQLTADLDGS FPYSHGDWIC FRQRLEHFAA NCEEAIIFLQ
721 NSFCSLNTHR TPRTAQEVAE LIDQHETMMK LVLEDPLLVS LRLEGGTVLA RLRREELGTE
781 DSRDTLEAAT SLYDRVDEEV HRLVLTSNNR LQQLEHLREL ASLLEGNDQQ SCQKGLQLAK
841 ENPQRTEEMV QDFRRGLSAV VSQAECREGE LARWTRSSEL CETVSSWMGP LDPEACPSSP
901 VAECLRSCHQ EATSVAAEAF PGAGVAVLKP HALGKPWASQ QDLWLQYPQT RLRLEEALSE
961 AAPDPSLPPL AQSPPKHERA QEAMRRHQKP PSFPSTDSGG GAWEPAQPLS GLPGRALLCG
1021 QDGETLRPGL CALWDPLSLL RGLPGAGATT AHLEDSSACS SEPTQTLASR PRKHPQKKMI
1081 KKTQSFEIPQ PDSGPRDSCQ PDHTSVFSKG LEVTSTVATE KKLPLWQHAR SPPVTQSRSL
1141 SSPSGLHPAE EDGRQQVGSS RLRHIMAEMI ATEREYIRCL GYVIDNYFPE MERMDLPQGL
1201 RGKHHVIFGN LEKLHDFHQQ HFLRELERCQ HCPLAVGRSF LRHEEQFGMY VIYSKNKPQS
1261 DALLSSHGNA FFKDKQRELG DKMDLASYLL RPVQRVAKYA LLLQDLLKEA SCGLAQGQEL
1321 GELRAAEVVV CFQLRHGNDL LAMDAIRGCD VNLKEQGQLR CRDEFIVCCG RKKYLRHVFL
1381 FEDLILFSKT QKVEGSHDVY LYKQSFKTAE IGMTENVGDS GLRFEIWFRR RRKSQDTYIL
1441 QASSAEVKSA WTDVIGRILW RQALKSRELR IQEMASMGIG NQPFMDVKPR DRTPDCAVIS
1501 DRAPKCAVMS DRVPDSIVKG TESQMRGSTA VSSSDHAAPF KRPHSTISDS STSSSSSQSS
1561 SILGSLGLLV SSSPAHPGLW SPAHSPWSSD IRACVEEDEP EPELETGTQA AVCEGAPAVL
1621 LSRTRQALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLEKHG4B 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)
- 0.48
- Highest tissue expression
- 7.9 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 7.9 nTPM
- pituitary gland: 3.4 nTPM
- thyroid gland: 3 nTPM
- testis: 2.8 nTPM
- salivary gland: 2.6 nTPM
- kidney: 2.3 nTPM
Single-cell type
- choroid plexus epithelial cells: 235 nCPM
- ependymal cells: 122 nCPM
- gonadotrophs: 108 nCPM
- pituitary stem cells: 68 nCPM
- renal collecting duct principal cells: 58 nCPM
- somatotrophs: 43 nCPM
Immune cell
- plasmacytoid DC: 1.9 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- choroid plexus: 21 nTPM
- thalamus: 5.9 nTPM
- amygdala: 4.2 nTPM
- white matter: 3.3 nTPM
- midbrain: 2.8 nTPM
- hypothalamus: 2.6 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)
- 1.22
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.27
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLEKHG4B 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 PLEKHG4B as an antibody target. Whether an autoantibody or antibody against PLEKHG4B could matter depends on whether native PLEKHG4B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLEKHG4B is annotated at the cell surface, where native PLEKHG4B 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 PLEKHG4B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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