MTX1
Metaxin-1
Also known as: MTX, MTX1_HUMAN, MTXN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13505
- Gene
- MTX1
- Ensembl
- ENSG00000173171
- Chromosome
- 1
- Canonical length
- 466 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Predicted to be involved in mitochondrion organization. Located in mitochondrion. Part of SAM complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
466 residues, UniProt reviewed canonical sequence.
>Q13505|MTX1
1 MLLGGPPRSP RSGTSPKGPW SSTGHVQFGK SPQTWPRRTR PRSPEPAAPS GVRGSTWTRR
61 RDSPRRAGPT ALSRYVGHLW MGRRPPSPEA RGPVPRSSAA SRARRSLASP GISPGPLTAT
121 IGGAVAGGGP RQGRAEAHKE VFPGQRVGKM AAPMELFCWS GGWGLPSVDL DSLAVLTYAR
181 FTGAPLKVHK ISNPWQSPSG TLPALRTSHG EVISVPHKII THLRKEKYNA DYDLSARQGA
241 DTLAFMSLLE EKLLPVLVHT FWIDTKNYVE VTRKWYAEAM PFPLNFFLPG RMQRQYMERL
301 QLLTGEHRPE DEEELEKELY REARECLTLL SQRLGSQKFF FGDAPASLDA FVFSYLALLL
361 QAKLPSGKLQ VHLRGLHNLC AYCTHILSLY FPWDGAEVPP QRQTPAGPET EEEPYRRRNQ
421 ILSVLAGLAA MVGYALLSGI VSIQRATPAR APGTRTLGMA EEDEEELocalizationUniProt · AlphaFold · HPA
Whether an antibody against MTX1 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)
- 0.46
- Highest tissue expression
- 87 nTPM
Expression across tissuesHPA
Tissue
- testis: 87 nTPM
- choroid plexus: 47 nTPM
- liver: 43 nTPM
- bone marrow: 37 nTPM
- parathyroid gland: 35 nTPM
- kidney: 33 nTPM
Single-cell type
- epicardial cells: 39 nCPM
- cardiomyocytes: 19 nCPM
- late spermatids: 12 nCPM
- kupffer cells: 8.2 nCPM
- adipocytes: 8.1 nCPM
- early spermatids: 7.8 nCPM
Immune cell
- neutrophil: 115 nTPM
- classical monocyte: 69 nTPM
- myeloid DC: 61 nTPM
- memory B-cell: 42 nTPM
- total PBMC: 41 nTPM
- T-reg: 39 nTPM
Brain region
- choroid plexus: 22 nTPM
- cerebellum: 13 nTPM
- white matter: 13 nTPM
- thalamus: 12 nTPM
- medulla oblongata: 12 nTPM
- midbrain: 12 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)
- 0.72
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.19
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- inner mitochondrial membrane organization
- lactation
- mitochondrion organization
- protein insertion into mitochondrial outer membrane
- protein transport
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
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MTX1 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 MTX1 as an antibody target. Whether an autoantibody or antibody against MTX1 could matter depends on whether native MTX1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MTX1 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 MTX1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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