RNF112
RING finger protein 112
Also known as: BFP, RN112_HUMAN, ZNF179
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9ULX5
- Gene
- RNF112
- Ensembl
- ENSG00000128482
- Chromosome
- 17
- Canonical length
- 631 aa
- Protein class
- Enzymes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
631 residues, UniProt reviewed canonical sequence.
>Q9ULX5|RNF112
1 MPRPALSVTS FCHRLGKRER KQSFMGNSGN SWSHTPFPKL ELGLGPQPMA PRELPTCSIC
61 LERLRDPISL DCGHDFCIRC FSTHRLPGCE PPCCPECRKI CKQKRGLRSL GEKMKLLPQR
121 PLPPALQETC PVRAEPLLLV RINASGGLIL RMGAINRCLK HPLARDTPVC LLAVLGEQHS
181 GKSFLLNHLL QGLPGLESGE GGRPRGGEAS LQGCRWGANG LARGIWMWSH PFLLGKEGKK
241 VAVFLVDTGD AMSPELSRET RIKLCALTTM LSSYQILSTS QELKDTDLDY LEMFVHVAEV
301 MGKHYGMVPI QHLDLLVRDS SHPNKAGQGH VGNIFQRLSG RYPKVQELLQ GKRARCCLLP
361 APGRRRMNQG HASPGDTDDD FRHLLGAYVS DVLSAAPQHA KSRCQGYWNE GRAVARGDRR
421 LLTGQQLAQE IKNLSGWMGR TGPGFTSPDE MAAQLHDLRK VEAAKREFEE YVRQQDVATK
481 RIFSALRVLP DTMRNLLSTQ KDAILARHGV ALLCKGRDQT LEALEAELQA TAKAFMDSYT
541 MRFCGHLAAV GGAVGAGLMG LAGGVVGAGM AAAALAAEAG MVAAGAAVGA TGAAVVGGGV
601 GAGLAATVGC MEKEEDERLL EGDREPLLQE ELocalizationUniProt · AlphaFold · HPA
Whether an antibody against RNF112 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
- 2
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 106 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 106 nTPM
- basal ganglia: 31 nTPM
- cerebral cortex: 31 nTPM
- hippocampal formation: 25 nTPM
- hypothalamus: 20 nTPM
- amygdala: 18 nTPM
Single-cell type
- brain excitatory neurons: 33 nCPM
- brain inhibitory neurons: 26 nCPM
- oligodendrocyte progenitor cells: 21 nCPM
- other brain neurons: 20 nCPM
- fibro-adipogenic progenitors: 11 nCPM
- müller glia: 11 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 59 nTPM
- cerebral cortex: 40 nTPM
- hippocampal formation: 40 nTPM
- white matter: 36 nTPM
- basal ganglia: 30 nTPM
- amygdala: 29 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)
- 0.54
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.5
- DepMap mean gene effect
- 0.26
- DepMap dependency class
- none
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
- embryonic brain development
- endoplasmic reticulum organization
- G1 to G0 transition involved in cell differentiation
- neuron differentiation
- positive regulation of glial cell differentiation
- positive regulation of neuron differentiation
- protein autoubiquitination
- protein homooligomerization
- regulation of cell cycle
- response to hydroperoxide
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, RING-type
- Zinc finger, RING/FYVE/PHD-type
- Guanylate-binding protein, N-terminal
- Zinc finger, C3HC4 RING-type
- P-loop containing nucleoside triphosphate hydrolase
- GB1/RHD3-type guanine nucleotide-binding (G) domain
- Zinc finger, C3HC4 type (RING finger)
- Guanylate-binding protein, N-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RNF112 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 RNF112 as an antibody target. Whether an autoantibody or antibody against RNF112 could matter depends on whether native RNF112 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RNF112 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 RNF112 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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