MTX3
Metaxin-3
Also known as: MTX3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5HYI7
- Gene
- MTX3
- Ensembl
- ENSG00000177034
- Chromosome
- 5
- Canonical length
- 312 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Predicted to be involved in mitochondrion organization. Located in mitochondrion. Part of MIB complex and SAM complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
312 residues, UniProt reviewed canonical sequence.
>Q5HYI7|MTX3
1 MAAPLELSCW GGGWGLPSVH SESLVVMAYA KFSGAPLKVN VIDNTWRGSR GDVPILTTED
61 DMVSQPAKIL NFLRKQKYNA DYELSAKQGA DTLAYIALLE EKLLPAVLHT FWVESDNYFT
121 VTKPWFASQI PFPLSLILPG RMSKGALNRI LLTRGQPPLY HLREVEAQIY RDAKECLNLL
181 SNRLGTSQFF FGDTPSTLDA YVFGFLAPLY KVRFPKVQLQ EHLKQLSNLC RFCDDILSSY
241 FRLSLGGISP AGQETVDANL QKLTQLVNKE SNLIEKMDDN LRQSPQLPPR KLPTLKLTPA
301 EEENNSFQRL SPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MTX3 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
- 0
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 11 nTPM
- retina: 11 nTPM
- ovary: 9.4 nTPM
- basal ganglia: 8.2 nTPM
- cerebellum: 7.9 nTPM
- lymph node: 7.7 nTPM
Single-cell type
- cone photoreceptor cells: 50 nCPM
- gonadotrophs: 42 nCPM
- retinal pigment epithelial cells: 38 nCPM
- adrenal medulla cells: 32 nCPM
- bergmann glia: 32 nCPM
- brain inhibitory neurons: 30 nCPM
Immune cell
- memory B-cell: 0.8 nTPM
- naive CD4 T-cell: 0.8 nTPM
- gdT-cell: 0.6 nTPM
- memory CD4 T-cell: 0.6 nTPM
- naive CD8 T-cell: 0.6 nTPM
- memory CD8 T-cell: 0.5 nTPM
Brain region
- cerebral cortex: 18 nTPM
- basal ganglia: 18 nTPM
- hypothalamus: 18 nTPM
- pons: 18 nTPM
- hippocampal formation: 18 nTPM
- midbrain: 17 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)
- 1.04
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.12
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
- Mitochondrial outer membrane transport complex Sam37/metaxin, N-terminal domain
- Metaxin, glutathione S-transferase domain
- Glutathione S-transferase, C-terminal domain superfamily
- Glutathione transferase family
- Mitochondrial Protein Transport Metaxin
- Outer mitochondrial membrane transport complex protein
- Glutathione S-transferase, C-terminal domain
- Mitochondrial outer membrane transport complex protein Metaxin 1/3
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MTX3 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 MTX3 as an antibody target. Whether an autoantibody or antibody against MTX3 could matter depends on whether native MTX3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MTX3 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 MTX3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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