ARHGEF19
Rho guanine nucleotide exchange factor 19
Also known as: ARHGJ_HUMAN, FLJ33962, WGEF
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IW93
- Gene
- ARHGEF19
- Ensembl
- ENSG00000142632
- Chromosome
- 1
- Canonical length
- 802 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear bodies
OverviewNCBI Gene
Guanine nucleotide exchange factors (GEFs) such as ARHGEF19 accelerate the GTPase activity of Rho GTPases (see RHOA, MIM 165390).[supplied by OMIM, Dec 2008]
Canonical amino-acid sequenceUniProt
802 residues, UniProt reviewed canonical sequence.
>Q8IW93|ARHGEF19
1 MDCGPPATLQ PHLTGPPGTA HHPVAVCQQE SLSFAELPAL KPPSPVCLDL FPVAPEELRA
61 PGSRWSLGTP APLQGLLWPL SPGGSDTEIT SGGMRPSRAG SWPHCPGAQP PALEGPWSPR
121 HTQPQRRASH GSEKKSAWRK MRVYQREEVP GCPEAHAVFL EPGQVVQEQA LSTEEPRVEL
181 SGSTRVSLEG PERRRFSASE LMTRLHSSLR LGRNSAARAL ISGSGTGAAR EGKASGMEAR
241 SVEMSGDRVS RPAPGDSREG DWSEPRLDTQ EEPPLGSRST NERRQSRFLL NSVLYQEYSD
301 VASARELRRQ QREEEGPGDE AEGAEEGPGP PRANLSPSSS FRAQRSARGS TFSLWQDIPD
361 VRGSGVLATL SLRDCKLQEA KFELITSEAS YIHSLSVAVG HFLGSAELSE CLGAQDKQWL
421 FSKLPEVKST SERFLQDLEQ RLEADVLRFS VCDVVLDHCP AFRRVYLPYV TNQAYQERTY
481 QRLLLENPRF PGILARLEES PVCQRLPLTS FLILPFQRIT RLKMLVENIL KRTAQGSEDE
541 DMATKAFNAL KELVQECNAS VQSMKRTEEL IHLSKKIHFE GKIFPLISQA RWLVRHGELV
601 ELAPLPAAPP AKLKLSSKAV YLHLFNDCLL LSRRKELGKF AVFVHAKMAE LQVRDLSLKL
661 QGIPGHVFLL QLLHGQHMKH QFLLRARTES EKQRWISALC PSSPQEDKEV ISEGEDCPQV
721 QCVRTYKALH PDELTLEKTD ILSVRTWTSD GWLEGVRLAD GEKGWVPQAY VEEISSLSAR
781 LRNLRENKRV TSATSKLGEA PVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGEF19 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)
- 0.43
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- skin: 27 nTPM
- salivary gland: 16 nTPM
- esophagus: 15 nTPM
- thyroid gland: 11 nTPM
- vagina: 11 nTPM
- cervix: 10 nTPM
Single-cell type
- paneth cells: 27 nCPM
- esophageal basal cells: 23 nCPM
- prostatic hillock cells: 21 nCPM
- esophageal apical cells: 21 nCPM
- respiratory deuterosomal cells: 21 nCPM
- respiratory basal cells: 19 nCPM
Immune cell
- gdT-cell: 0.9 nTPM
- MAIT T-cell: 0.9 nTPM
- memory CD4 T-cell: 0.8 nTPM
- naive CD4 T-cell: 0.8 nTPM
- NK-cell: 0.8 nTPM
- memory B-cell: 0.7 nTPM
Brain region
- hypothalamus: 1.3 nTPM
- medulla oblongata: 1.3 nTPM
- amygdala: 1.2 nTPM
- choroid plexus: 1.1 nTPM
- midbrain: 1.1 nTPM
- cerebral cortex: 1 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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.97
- DepMap mean gene effect
- 0
- 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
- regulation of actin cytoskeleton organization
- regulation of small GTPase mediated signal transduction
- Wnt signaling pathway, planar cell polarity pathway
- wound healing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ARHGEF19 as an antibody target. Whether an autoantibody or antibody against ARHGEF19 could matter depends on whether native ARHGEF19 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGEF19 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 ARHGEF19 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...