GARNL3
GTPase-activating Rap/Ran-GAP domain-like protein 3
Also known as: bA356B19.1, DKFZp761J1523, GARL3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VVW2
- Gene
- GARNL3
- Ensembl
- ENSG00000136895
- Chromosome
- 9
- Canonical length
- 1013 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1013 residues, UniProt reviewed canonical sequence.
>Q5VVW2|GARNL3
1 MVVDFCRRFV ARSLCIILMK HFCSSSVSED LGCRRGDFSR KHYGSVELLI SSDADGAIQR
61 AGRFRVENGS SDENATALPG TWRRTDVHLE NPEYHTRWYF KYFLGQVHQN YIGNDAEKSP
121 FFLSVTLSDQ NNQRVPQYRA ILWRKTGTQK ICLPYSPTKT LSVKSILSAM NLDKFEKGPR
181 EIFHPEIQKD LLVLEEQEGS VNFKFGVLFA KDGQLTDDEM FSNEIGSEPF QKFLNLLGDT
241 ITLKGWTGYR GGLDTKNDTT GIHSVYTVYQ GHEIMFHVST MLPYSKENKQ QVERKRHIGN
301 DIVTIVFQEG EESSPAFKPS MIRSHFTHIF ALVRYNQQND NYRLKIFSEE SVPLFGPPLP
361 TPPVFTDHQE FRDFLLVKLI NGEKATLETP TFAQKRRRTL DMLIRSLHQD LMPDLHKNML
421 NRRSFSDVLP ESPKSARKKE EARQAEFVRI GQALKLKSIV RGDAPSSLAA SGICKKEPWE
481 PQCFCSNFPH EAVCADPWGQ ALLVSTDAGV LLVDDDLPSV PVFDRTLPVK QMHVLETLDL
541 LVLRADKGKD ARLFVFRLSA LQKGLEGKQA GKSRSDCREN KLEKTKGCHL YAINTHHSRE
601 LRIVVAIRNK LLLITRKHNK PSGVTSTSLL SPLSESPVEE FQYIREICLS DSPMVMTLVD
661 GPAEESDNLI CVAYRHQFDV VNESTGEAFR LHHVEANRVN FVAAIDVYED GEAGLLLCYN
721 YSCIYKKVCP FNGGSFLVQP SASDFQFCWN QAPYAIVCAF PYLLAFTTDS MEIRLVVNGN
781 LVHTAVVPQL QLVASRSDIY FTATAAVNEV SSGGSSKGAS ARNSPQTPPG RDTPVFPSSL
841 GEGEIQSKNL YKIPLRNLVG RSIERPLKSP LVSKVITPPT PISVGLAAIP VTHSLSLSRM
901 EIKEIASRTR RELLGLSDEG GPKSEGAPKA KSKPRKRLEE SQGGPKPGAV RSSSSDRIPS
961 GSLESASTSE ANPEGHSASS DQDPVADREG SPVSGSSPFQ LTAFSDEDII DLKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GARNL3 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 20 nTPM
- blood vessel: 19 nTPM
- cerebral cortex: 12 nTPM
- heart muscle: 11 nTPM
- amygdala: 10 nTPM
- endometrium: 9 nTPM
Single-cell type
- adrenal medulla cells: 266 nCPM
- endometrial stromal cells: 236 nCPM
- cardiomyocytes: 221 nCPM
- astrocytes: 221 nCPM
- oligodendrocytes: 208 nCPM
- brain excitatory neurons: 204 nCPM
Immune cell
- plasmacytoid DC: 1 nTPM
- gdT-cell: 0.3 nTPM
- memory CD8 T-cell: 0.3 nTPM
- naive CD4 T-cell: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- myeloid DC: 0.1 nTPM
Brain region
- cerebellum: 34 nTPM
- white matter: 32 nTPM
- cerebral cortex: 24 nTPM
- pons: 22 nTPM
- basal ganglia: 21 nTPM
- hypothalamus: 20 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about GARNL3.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 129 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)
- 0.5
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.02
- DepMap mean gene effect
- -0.05
- 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
Molecular functions
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GARNL3 as an antibody target. Whether an autoantibody or antibody against GARNL3 could matter depends on whether native GARNL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GARNL3 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 GARNL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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