MEAK7
MTOR-associated protein MEAK7
Also known as: KIAA1609, mEAK-7, MEAK7_HUMAN, TLDC1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P9B6
- Gene
- MEAK7
- Ensembl
- ENSG00000140950
- Chromosome
- 16
- Canonical length
- 456 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Cytosol
OverviewNCBI Gene
Involved in several processes, including TOR signaling; positive regulation of protein localization to lysosome; and response to insulin. Located in cytosol; lysosomal membrane; and nuclear lumen. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
456 residues, UniProt reviewed canonical sequence.
>Q6P9B6|MEAK7
1 MGNSRSRVGR SFCSQFLPEE QAEIDQLFDA LSSDKNSPNV SSKSFSLKAL QNHVGEALPP
61 EMVTRLYDGM RRVDLTGKAK GPSENVSQEQ FTASMSHLLK GNSEEKSLMI MKMISATEGP
121 VKAREVQKFT EDLVGSVVHV LSHRQELRGW TGKEAPGPNP RVQVLAAQLL SDMKLQDGKR
181 LLGPQWLDYD CDRAVIEDWV FRVPHVAIFL SVVICKGFLI LCSSLDLTTL VPERQVDQGR
241 GFESILDVLS VMYINAQLPR EQRHRWCLLF SSELHGHSFS QLCGHITHRG PCVAVLEDHD
301 KHVFGGFASC SWEVKPQFQG DNRCFLFSIC PSMAVYTHTG YNDHYMYLNH GQQTIPNGLG
361 MGGQHNYFGL WVDVDFGKGH SRAKPTCTTY NSPQLSAQEN FQFDKMEVWA VGDPSEEQLA
421 KGNKSILDAD PEAQALLEIS GHSRHSEGLR EVPDDELocalizationUniProt · AlphaFold · HPA
Whether an antibody against MEAK7 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)
- 0.28
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 12 nTPM
- placenta: 10 nTPM
- skin: 7.2 nTPM
- parathyroid gland: 6.9 nTPM
- urinary bladder: 6.8 nTPM
- cervix: 6.3 nTPM
Single-cell type
- cone photoreceptor cells: 149 nCPM
- rod photoreceptor cells: 96 nCPM
- esophageal suprabasal cells: 77 nCPM
- syncytiotrophoblasts: 75 nCPM
- esophageal apical cells: 65 nCPM
- cytotrophoblasts: 61 nCPM
Immune cell
- basophil: 17 nTPM
- T-reg: 7.9 nTPM
- naive CD4 T-cell: 6.1 nTPM
- memory CD4 T-cell: 5.6 nTPM
- memory CD8 T-cell: 4.6 nTPM
- eosinophil: 3.9 nTPM
Brain region
- pons: 18 nTPM
- choroid plexus: 18 nTPM
- hippocampal formation: 17 nTPM
- amygdala: 16 nTPM
- basal ganglia: 16 nTPM
- white matter: 15 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)
- 1.78
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.05
- 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
- negative regulation of cellular response to oxidative stress
- positive regulation of protein localization to lysosome
- regulation of cell migration
- regulation of cell population proliferation
- response to amino acid
- response to insulin
- response to nutrient levels
- response to oxidative stress
- TOR signaling
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MEAK7 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 MEAK7 as an antibody target. Whether an autoantibody or antibody against MEAK7 could matter depends on whether native MEAK7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MEAK7 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 MEAK7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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