ARMCX3
Armadillo repeat-containing X-linked protein 3
Also known as: ALEX3, ARMX3_HUMAN, GASP6
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UH62
- Gene
- ARMCX3
- Ensembl
- ENSG00000102401
- Chromosome
- X
- Canonical length
- 379 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Cytosol
OverviewNCBI Gene
This gene encodes a member of the ALEX family of proteins which may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and a single Armadillo (arm) repeat. Other proteins containing the arm repeat are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is closely localized with other family members on the X chromosome. Three transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
379 residues, UniProt reviewed canonical sequence.
>Q9UH62|ARMCX3
1 MGYARKVGWV TAGLVIGAGA CYCIYRLTRG RKQNKEKMAE GGSGDVDDAG DCSGARYNDW
61 SDDDDDSNES KSIVWYPPWA RIGTEAGTRA RARARARATR ARRAVQKRAS PNSDDTVLSP
121 QELQKVLCLV EMSEKPYILE AALIALGNNA AYAFNRDIIR DLGGLPIVAK ILNTRDPIVK
181 EKALIVLNNL SVNAENQRRL KVYMNQVCDD TITSRLNSSV QLAGLRLLTN MTVTNEYQHM
241 LANSISDFFR LFSAGNEETK LQVLKLLLNL AENPAMTREL LRAQVPSSLG SLFNKKENKE
301 VILKLLVIFE NINDNFKWEE NEPTQNQFGE GSLFFFLKEF QVCADKVLGI ESHHDFLVKV
361 KVGKFMAKLA EHMFPKSQELocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARMCX3 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)
- 0.35
- Highest tissue expression
- 99 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 99 nTPM
- parathyroid gland: 97 nTPM
- tongue: 59 nTPM
- salivary gland: 56 nTPM
- adrenal gland: 56 nTPM
- pancreas: 51 nTPM
Single-cell type
- epididymal principal cells: 328 nCPM
- platelets: 283 nCPM
- syncytiotrophoblasts: 151 nCPM
- epididymal clear cells: 137 nCPM
- mast cells: 136 nCPM
- plasma cells: 136 nCPM
Immune cell
- basophil: 44 nTPM
- plasmacytoid DC: 26 nTPM
- MAIT T-cell: 18 nTPM
- non-classical monocyte: 17 nTPM
- intermediate monocyte: 16 nTPM
- myeloid DC: 16 nTPM
Brain region
- hypothalamus: 68 nTPM
- white matter: 64 nTPM
- spinal cord: 62 nTPM
- cerebral cortex: 62 nTPM
- cerebellum: 61 nTPM
- thalamus: 61 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)
- 0.84
- gnomAD pLI
- 0.46
- gnomAD missense Z
- 1.74
- DepMap mean gene effect
- 0.01
- 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
- axonal transport of mitochondrion
- intracellular protein localization
- mitochondrion organization
- positive regulation of transcription by RNA polymerase II
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARMCX3 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 ARMCX3 as an antibody target. Whether an autoantibody or antibody against ARMCX3 could matter depends on whether native ARMCX3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARMCX3 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 ARMCX3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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