NEMF
Ribosome quality control complex subunit NEMF
Also known as: FLJ10051, NEMF_HUMAN, NY-CO-1, RQC2, SDCCAG1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60524
- Gene
- NEMF
- Ensembl
- ENSG00000165525
- Chromosome
- 14
- Canonical length
- 1076 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies,Cytosol
OverviewNCBI Gene
This gene encodes a component of the ribosome quality control complex. The encoded protein facilitates the recognition and ubiquitination of stalled 60S subunits by the ubiquitin ligase listerin. A similar protein in fly functions as a tumor suppressor. [provided by RefSeq, Jul 2016]
Canonical amino-acid sequenceUniProt
1076 residues, UniProt reviewed canonical sequence.
>O60524|NEMF
1 MKSRFSTIDL RAVLAELNAS LLGMRVNNVY DVDNKTYLIR LQKPDFKATL LLESGIRIHT
61 TEFEWPKNMM PSSFAMKCRK HLKSRRLVSA KQLGVDRIVD FQFGSDEAAY HLIIELYDRG
121 NIVLTDYEYV ILNILRFRTD EADDVKFAVR ERYPLDHARA AEPLLTLERL TEIVASAPKG
181 ELLKRVLNPL LPYGPALIEH CLLENGFSGN VKVDEKLETK DIEKVLVSLQ KAEDYMKTTS
241 NFSGKGYIIQ KREIKPSLEA DKPVEDILTY EEFHPFLFSQ HSQCPYIEFE SFDKAVDEFY
301 SKIEGQKIDL KALQQEKQAL KKLDNVRKDH ENRLEALQQA QEIDKLKGEL IEMNLQIVDR
361 AIQVVRSALA NQIDWTEIGL IVKEAQAQGD PVASAIKELK LQTNHVTMLL RNPYLLSEEE
421 DDDVDGDVNV EKNETEPPKG KKKKQKNKQL QKPQKNKPLL VDVDLSLSAY ANAKKYYDHK
481 RYAAKKTQKT VEAAEKAFKS AEKKTKQTLK EVQTVTSIQK ARKVYWFEKF LWFISSENYL
541 IIGGRDQQQN EIIVKRYLTP GDIYVHADLH GATSCVIKNP TGEPIPPRTL TEAGTMALCY
601 SAAWDARVIT SAWWVYHHQV SKTAPTGEYL TTGSFMIRGK KNFLPPSYLM MGFSFLFKVD
661 ESCVWRHQGE RKVRVQDEDM ETLASCTSEL ISEEMEQLDG GDTSSDEDKE EHETPVEVEL
721 MTQVDQEDIT LQSGRDELNE ELIQEESSED EGEYEEVRKD QDSVGEMKDE GEETLNYPDT
781 TIDLSHLQPQ RSIQKLASKE ESSNSSDSKS QSRRHLSAKE RREMKKKKLP SDSGDLEALE
841 GKDKEKESTV HIETHQNTSK NVAAVQPMKR GQKSKMKKMK EKYKDQDEED RELIMKLLGS
901 AGSNKEEKGK KGKKGKTKDE PVKKQPQKPR GGQRVSDNIK KETPFLEVIT HELQDFAVDD
961 PHDDKEEQDL DQQGNEENLF DSLTGQPHPE DVLLFAIPIC APYTTMTNYK YKVKLTPGVQ
1021 KKGKAAKTAL NSFMHSKEAT AREKDLFRSV KDTDLSRNIP GKVKVSAPNL LNVKRKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NEMF 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)
- 0.41
- Highest tissue expression
- 40 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 40 nTPM
- parathyroid gland: 23 nTPM
- esophagus: 21 nTPM
- skeletal muscle: 21 nTPM
- cerebral cortex: 21 nTPM
- tongue: 20 nTPM
Single-cell type
- esophageal apical cells: 306 nCPM
- myonuclei: 290 nCPM
- renal collecting duct intercalated cells: 205 nCPM
- retinal horizontal cells: 202 nCPM
- sertoli cells: 177 nCPM
- b-cells: 173 nCPM
Immune cell
- naive B-cell: 87 nTPM
- memory B-cell: 84 nTPM
- plasmacytoid DC: 80 nTPM
- basophil: 77 nTPM
- neutrophil: 62 nTPM
- naive CD8 T-cell: 59 nTPM
Brain region
- cerebellum: 62 nTPM
- white matter: 60 nTPM
- basal ganglia: 51 nTPM
- medulla oblongata: 49 nTPM
- pons: 49 nTPM
- midbrain: 49 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about NEMF.
Disease | AllUniProt
Conditions NEMF is implicated in, by any mechanism.
- Intellectual developmental disorder with speech delay and axonal peripheral neuropathy (IDDSAPN) MIM:619099
Disease | GeneticClinVar
29 pathogenic / likely-pathogenic of 233 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Intellectual developmental disorder with speech delay and axonal peripheral neuropathy
- See cases
- Inborn genetic diseases
- NEMF-related disorder
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)
- 0.42
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.19
- DepMap mean gene effect
- -0.18
- 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
- nuclear export
- protein-containing complex assembly
- rescue of stalled ribosome
- ribosome-associated ubiquitin-dependent protein catabolic process
- CAT tailing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- NFACT, RNA-binding domain
- NFACT protein RNA binding domain
- NFACT protein, C-terminal
- Ribosome Quality Control Complex Subunit NEMF
- NFACT N-terminal and middle domains
- NFACT protein C-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NEMF 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 NEMF as an antibody target. Whether an autoantibody or antibody against NEMF could matter depends on whether native NEMF is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NEMF 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 NEMF as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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