ARMH3
Armadillo-like helical domain-containing protein 3
Also known as: ARMD3_HUMAN, C10orf76, FLJ13114
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5T2E6
- Gene
- ARMH3
- Ensembl
- ENSG00000120029
- Chromosome
- 10
- Canonical length
- 689 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Involved in regulation of Golgi organization. Located in Golgi membrane and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
689 residues, UniProt reviewed canonical sequence.
>Q5T2E6|ARMH3
1 MAQVEKRGGL LRKSSASKKP LKEKVVLMYD EIFMTEDPSK CSPRFWEELF LMKVNLEYLE
61 GKLESLDGEE LMKIKDNINC LFQHCIQALG EEHPIRVVNA LQTLCALIRG VHQKNKSTSG
121 FDIINMLMGF DKAELCMKNL MESLDSLLCA EGSESLKSLC LKLLLCLVTV TDNISQNTIL
181 EYVMINSIFE AILQILSHPP SRREHGYDAV VLLALLVNYR KYESVNPYIV KLSIVDDEAT
241 LNGMGLVIAQ ALSEYNRQYK DKEEEHQSGF FSALTNMVGS MFIADAHEKI SVQTNEAILL
301 ALYEAVHLNR NFITVLAQSH PEMGLVTTPV SPAPTTPVTP LGTTPPSSDV ISSVELPLDA
361 DVQTSNLLIT FLKYSSIVMQ DTKDEHRLHS GKLCLIILTC IAEDQYANAF LHDDNMNFRV
421 NLHRMPMRHR KKAADKNLPC RPLVCAVLDL MVEFIVTHMM KEFPMDLYIR CIQVVHKLLC
481 YQKKCRVRLH YTWRELWSAL INLLKFLMSN ETVLLAKHNI FTLALMIVNL FNMFITYGDT
541 FLPTPSSYDE LYYEIIRMHQ SFDNLYSMVL RLSTNAGQWK EAASKVTHAL VNIRAIINHF
601 NPKIESYAAV NHISQLSEEQ VLEVVRANYD TLTLKLQDGL DQYERYSEQH KEAAFFKELV
661 RSISTNVRRN LAFHTLSQEV LLKEFSTISLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARMH3 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 21 nTPM
- tongue: 19 nTPM
- skeletal muscle: 19 nTPM
- heart muscle: 16 nTPM
- parathyroid gland: 15 nTPM
- retina: 15 nTPM
Single-cell type
- myonuclei: 357 nCPM
- cone photoreceptor cells: 273 nCPM
- adipocytes: 268 nCPM
- microglia: 225 nCPM
- neutrophil progenitors: 209 nCPM
- cardiomyocytes: 195 nCPM
Immune cell
- basophil: 20 nTPM
- non-classical monocyte: 11 nTPM
- intermediate monocyte: 8.7 nTPM
- myeloid DC: 7.7 nTPM
- eosinophil: 7.5 nTPM
- plasmacytoid DC: 7.4 nTPM
Brain region
- cerebellum: 33 nTPM
- midbrain: 30 nTPM
- choroid plexus: 29 nTPM
- basal ganglia: 28 nTPM
- white matter: 27 nTPM
- hypothalamus: 27 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)
- 0.57
- gnomAD pLI
- 0
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Armadillo-type fold
- Armadillo-like helical domain-containing protein 3, C-terminal
- Armadillo-like helical domain-containing protein 3-like
- Armadillo-like helical domain-containing protein 3, C-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARMH3 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 ARMH3 as an antibody target. Whether an autoantibody or antibody against ARMH3 could matter depends on whether native ARMH3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARMH3 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 ARMH3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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