RUNDC3A
RUN domain-containing protein 3A
Also known as: RAP2IP, RPIP8, RUN3A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q59EK9
- Gene
- RUNDC3A
- Ensembl
- ENSG00000108309
- Chromosome
- 17
- Canonical length
- 446 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to enable GTPase regulator activity. Predicted to be involved in positive regulation of cGMP-mediated signaling. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
446 residues, UniProt reviewed canonical sequence.
>Q59EK9|RUNDC3A
1 MEASFVQTTM ALGLSSKKAS SRNVAVERKN LITVCRFSVK TLLEKYTAEP IDDSSEEFVN
61 FAAILEQILS HRFKACAPAG PVSWFSSDGQ RGFWDYIRLA CSKVPNNCVS SIENMENIST
121 ARAKGRAWIR VALMEKRMSE YITTALRDTR TTRRFYDSGA IMLRDEATIL TGMLIGLSAI
181 DFSFCLKGEV LDGKTPVVID YTPYLKFTQS YDYLTDEEER HSAESSTSED NSPEHPYLPL
241 VTDEDSWYSK WHKMEQKFRI VYAQKGYLEE LVRLRESQLK DLEAENRRLQ LQLEEAAAQN
301 QREKRELEGV ILELQEQLTG LIPSDHAPLA QGSKELTTPL VNQWPSLGTL NGAEGASNSK
361 LYRRHSFMST EPLSAEASLS SDSQRLGEGT RDEEPWGPIG KDPTPSMLGL CGSLASIPSC
421 KSLASFKSNE CLVSDSPEGS PALSPSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RUNDC3A 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)
- 0.5
- Highest tissue expression
- 298 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 298 nTPM
- hippocampal formation: 241 nTPM
- amygdala: 227 nTPM
- cerebellum: 180 nTPM
- basal ganglia: 154 nTPM
- hypothalamus: 112 nTPM
Single-cell type
- late spermatids: 150 nCPM
- brain excitatory neurons: 63 nCPM
- erythrocytes: 49 nCPM
- other brain neurons: 48 nCPM
- brain inhibitory neurons: 43 nCPM
- corticotrophs: 34 nCPM
Immune cell
- memory CD4 T-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 283 nTPM
- hippocampal formation: 260 nTPM
- amygdala: 222 nTPM
- basal ganglia: 214 nTPM
- white matter: 189 nTPM
- pons: 141 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)
- 0.44
- gnomAD pLI
- 0.64
- gnomAD missense Z
- 2.69
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
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
- RUN domain
- RUN domain superfamily
- RUN domain-containing protein 3A/B
- RUN domain
- RUN domain-containing protein 3A, RUN domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RUNDC3A 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 RUNDC3A as an antibody target. Whether an autoantibody or antibody against RUNDC3A could matter depends on whether native RUNDC3A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RUNDC3A 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 RUNDC3A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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