METTL17
Ribosome assembly protein METTL17, mitochondrial
Also known as: FLJ20859, MET17_HUMAN, METT11D1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H7H0
- Gene
- METTL17
- Ensembl
- ENSG00000165792
- Chromosome
- 14
- Canonical length
- 456 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables 4 iron, 4 sulfur cluster binding activity. Involved in mitochondrial small ribosomal subunit assembly. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
456 residues, UniProt reviewed canonical sequence.
>Q9H7H0|METTL17
1 MAAALKCLLT LGRWCPGLGV APQARALAAL VPGVTQVDNK SGFLQKRPHR QHPGILKLPH
61 VRLPQALANG AQLLLLGSAG PTMENQVQTL TSYLWSRHLP VEPEELQRRA RHLEKKFLEN
121 PDLSQTEEKL RGAVLHALRK TTYHWQELSY TEGLSLVYMA ARLDGGFAAV SRAFHEIRAR
181 NPAFQPQTLM DFGSGTGSVT WAAHSIWGQS LREYMCVDRS AAMLVLAEKL LKGGSESGEP
241 YIPGVFFRQF LPVSPKVQFD VVVSAFSLSE LPSKADRTEV VQTLWRKTGH FLVLVENGTK
301 AGHSLLMDAR DLVLKGKEKS PLDPRPGFVF APCPHELPCP QLTNLACSFS QAYHPIPFSW
361 NKKPKEEKFS MVILARGSPE EAHRWPRITQ PVLKRPRHVH CHLCCPDGHM QHAVLTARRH
421 GRDLYRCARV SSWGDLLPVL TPSAFPPSTA QDPSESLocalizationUniProt · AlphaFold · HPA
Whether an antibody against METTL17 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)
- 0.3
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 34 nTPM
- tongue: 27 nTPM
- heart muscle: 26 nTPM
- skeletal muscle: 26 nTPM
- bone marrow: 25 nTPM
- spleen: 23 nTPM
Single-cell type
- ocular epithelial cells: 108 nCPM
- adrenal cortex cells: 107 nCPM
- early spermatids: 49 nCPM
- tuft cells: 46 nCPM
- leydig cells: 45 nCPM
- esophageal basal cells: 44 nCPM
Immune cell
- basophil: 29 nTPM
- myeloid DC: 17 nTPM
- memory B-cell: 14 nTPM
- memory CD8 T-cell: 13 nTPM
- memory CD4 T-cell: 13 nTPM
- naive CD4 T-cell: 12 nTPM
Brain region
- choroid plexus: 13 nTPM
- cerebral cortex: 12 nTPM
- cerebellum: 11 nTPM
- white matter: 11 nTPM
- medulla oblongata: 10 nTPM
- thalamus: 10 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)
- 1.06
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- -0.51
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- 4 iron, 4 sulfur cluster binding
- metal ion binding
- mitochondrial ribosome binding
- S-adenosyl-L-methionine binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- S-adenosyl-L-methionine-dependent methyltransferase superfamily
- Ribosomal protein Rsm22-like
- Mitochondrial RNA Methyltransferase
- Mitochondrial small ribosomal subunit Rsm22
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of METTL17 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 METTL17 as an antibody target. Whether an autoantibody or antibody against METTL17 could matter depends on whether native METTL17 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
METTL17 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 METTL17 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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