MLF1
Myeloid leukemia factor 1
Also known as: MLF1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P58340
- Gene
- MLF1
- Ensembl
- ENSG00000178053
- Chromosome
- 3
- Canonical length
- 268 aa
- Protein class
- Cancer-related genes, Disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Plasma membrane,Focal adhesion sites,Centrosome,Basal body,Cytosol,Mid piece,Principal piece,End piece
OverviewNCBI Gene
This gene encodes an oncoprotein which is thought to play a role in the phenotypic determination of hemopoetic cells. Translocations between this gene and nucleophosmin have been associated with myelodysplastic syndrome and acute myeloid leukemia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]
Canonical amino-acid sequenceUniProt
268 residues, UniProt reviewed canonical sequence.
>P58340|MLF1
1 MFRMLNSSFE DDPFFSESIL AHRENMRQMI RSFSEPFGRD LLSISDGRGR AHNRRGHNDG
61 EDSLTHTDVS SFQTMDQMVS NMRNYMQKLE RNFGQLSVDP NGHSFCSSSV MTYSKIGDEP
121 PKVFQASTQT RRAPGGIKET RKAMRDSDSG LEKMAIGHHI HDRAHVIKKS KNKKTGDEEV
181 NQEFINMNES DAHAFDEEWQ SEVLKYKPGR HNLGNTRMRS VGHENPGSRE LKRREKPQQS
241 PAIEHGRRSN VLGDKLHIKG SSVKSNKKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MLF1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 340 nTPM
Expression across tissuesHPA
Tissue
- testis: 340 nTPM
- skeletal muscle: 171 nTPM
- heart muscle: 118 nTPM
- tongue: 100 nTPM
- choroid plexus: 91 nTPM
- fallopian tube: 64 nTPM
Single-cell type
- late spermatids: 19,792 nCPM
- early spermatids: 5,555 nCPM
- late primary spermatocytes: 2,733 nCPM
- early primary spermatocytes: 484 nCPM
- fallopian tube ciliated cells: 467 nCPM
- epididymal efferent duct ciliated cells: 434 nCPM
Immune cell
- T-reg: 8.8 nTPM
- memory CD4 T-cell: 6.9 nTPM
- memory CD8 T-cell: 6.9 nTPM
- naive CD8 T-cell: 3.3 nTPM
- gdT-cell: 2.8 nTPM
- total PBMC: 2 nTPM
Brain region
- choroid plexus: 53 nTPM
- medulla oblongata: 34 nTPM
- midbrain: 33 nTPM
- white matter: 30 nTPM
- spinal cord: 26 nTPM
- basal ganglia: 21 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)
- 1.22
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.59
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA-templated transcription
- myeloid progenitor cell differentiation
- regulation of cell cycle G1/S phase transition
- regulation of DNA-templated transcription
- regulation of signal transduction by p53 class mediator
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MLF1 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 MLF1 as an antibody target. Whether an autoantibody or antibody against MLF1 could matter depends on whether native MLF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MLF1 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 MLF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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