Human Gene RNF19A (ENST00000341084.7_7) from GENCODE V47lift37
  Description: ring finger protein 19A, RBR E3 ubiquitin protein ligase, transcript variant 1 (from RefSeq NM_183419.4)
Gencode Transcript: ENST00000341084.7_7
Gencode Gene: ENSG00000034677.13_11
Transcript (Including UTRs)
   Position: hg19 chr8:101,269,295-101,322,181 Size: 52,887 Total Exon Count: 10 Strand: -
Coding Region
   Position: hg19 chr8:101,270,784-101,300,402 Size: 29,619 Coding Exon Count: 9 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr8:101,269,295-101,322,181)mRNA (may differ from genome)Protein (838 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsHGNC
MalacardsMGIOMIMPubMedReactomeUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: RN19A_HUMAN
DESCRIPTION: RecName: Full=E3 ubiquitin-protein ligase RNF19A; EC=6.3.2.-; AltName: Full=Double ring-finger protein; Short=Dorfin; AltName: Full=RING finger protein 19A; AltName: Full=p38;
FUNCTION: E3 ubiquitin-protein ligase which accepts ubiquitin from E2 ubiquitin-conjugating enzymes UBE2L3 and UBE2L6 in the form of a thioester and then directly transfers the ubiquitin to targeted substrates, such as SNCAIP or CASR. Specifically ubiquitinates pathogenic SOD1 variants, which leads to their proteasomal degradation and to neuronal protection.
PATHWAY: Protein modification; protein ubiquitination.
SUBUNIT: Interacts with UBE2L3 and UBE2L6. Interacts with transcription factor Sp1. Interacts with VCP, CASR, SNCAIP and with some SOD1 variants which cause amyotrophic lateral sclerosis, but not with wild-type SOD1.
SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein (Potential). Cytoplasm, cytoskeleton, centrosome. Note=Present in the hyaline inclusion bodies specifically found in motor neurons from amyotrophic lateral sclerosis patients. Present in the Lewy bodies specifically found in neurons from Parkinson disease patients.
TISSUE SPECIFICITY: Widely expressed, with highest levels in heart. Ubiquitously expressed in the central nervous system.
PTM: Phosphorylated upon DNA damage, probably by ATM or ATR.
SIMILARITY: Belongs to the RBR family. RNF19 subfamily.
SIMILARITY: Contains 1 IBR-type zinc finger.
SIMILARITY: Contains 2 RING-type zinc fingers.
SEQUENCE CAUTION: Sequence=BAB14581.1; Type=Erroneous initiation; Sequence=BAB15647.1; Type=Erroneous initiation;

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: RNF19A
Diseases sorted by gene-association score: lateral sclerosis (14), amyotrophic lateral sclerosis 1 (4), parkinson disease, late-onset (2)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 30.55 RPKM in Cells - EBV-transformed lymphocytes
Total median expression: 427.45 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -51.70180-0.287 Picture PostScript Text
3' UTR -339.901489-0.228 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR002867 - Znf_C6HC
IPR001841 - Znf_RING
IPR013083 - Znf_RING/FYVE/PHD

Pfam Domains:
PF01485 - IBR domain, a half RING-finger domain

SCOP Domains:
57850 - RING/U-box

ModBase Predicted Comparative 3D Structure on Q9NV58
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologGenome BrowserNo ortholog
Gene DetailsGene Details  Gene Details 
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 RGDEnsembl WormBase 
    Protein Sequence 
    Alignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0004842 ubiquitin-protein transferase activity
GO:0008134 transcription factor binding
GO:0016740 transferase activity
GO:0031624 ubiquitin conjugating enzyme binding
GO:0046872 metal ion binding
GO:0061630 ubiquitin protein ligase activity

Biological Process:
GO:0000209 protein polyubiquitination
GO:0000226 microtubule cytoskeleton organization
GO:0016567 protein ubiquitination
GO:0032436 positive regulation of proteasomal ubiquitin-dependent protein catabolic process

Cellular Component:
GO:0000151 ubiquitin ligase complex
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005815 microtubule organizing center
GO:0005829 cytosol
GO:0005856 cytoskeleton
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  BC062676 - Homo sapiens ring finger protein 19, mRNA (cDNA clone IMAGE:6652005).
BC105300 - Homo sapiens ring finger protein 19A, mRNA (cDNA clone IMAGE:6557603), partial cds.
AB029316 - Homo sapiens mRNA for ring-IBR-ring domain containing protein Dorfin, complete cds.
BC043648 - Homo sapiens ring finger protein 19A, mRNA (cDNA clone IMAGE:5277287), partial cds.
AL110253 - Homo sapiens mRNA; cDNA DKFZp566B1346 (from clone DKFZp566B1346).
AK023455 - Homo sapiens cDNA FLJ13393 fis, clone PLACE1001294, moderately similar to Mus musculus XY body protein (Xybp) mRNA.
AL122096 - Homo sapiens mRNA; cDNA DKFZp434M1115 (from clone DKFZp434M1115).
AK027070 - Homo sapiens cDNA: FLJ23417 fis, clone HEP20868.
JD062935 - Sequence 43959 from Patent EP1572962.
JD550855 - Sequence 531879 from Patent EP1572962.
JD429376 - Sequence 410400 from Patent EP1572962.
JD042571 - Sequence 23595 from Patent EP1572962.
JD082233 - Sequence 63257 from Patent EP1572962.
BC093938 - Homo sapiens ring finger protein 19A, mRNA (cDNA clone MGC:120973 IMAGE:7939783), complete cds.
BC093940 - Homo sapiens ring finger protein 19A, mRNA (cDNA clone MGC:120975 IMAGE:7939785), complete cds.
JD284864 - Sequence 265888 from Patent EP1572962.
KJ898566 - Synthetic construct Homo sapiens clone ccsbBroadEn_07960 RNF19A gene, encodes complete protein.
AJ242975 - Homo sapiens partial mRNA for putative protein p38 interacting with transcription factor Sp1.
AK001774 - Homo sapiens cDNA FLJ10912 fis, clone OVARC1000151, weakly similar to partial mRNA for putative protein p38 interacting with transcription factor Sp1.
AK057699 - Homo sapiens cDNA FLJ33137 fis, clone UTERU1000077, moderately similar to GAMETOGENESIS EXPRESSED PROTEIN GEG-154.
AB271913 - Homo sapiens RNF19 mRNA for RING finger protein 19 isoform, partial cds, isolate: RNF19-Iso1.
AB271914 - Homo sapiens RNF19 mRNA for RING finger protein 19 isoform, partial cds, isolate: RNF19-Iso2.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein Q9NV58 (Reactome details) participates in the following event(s):

R-HSA-983157 Interaction of E3 with substrate and E2-Ub complex
R-HSA-983147 Release of E3 from polyubiquitinated substrate
R-HSA-983140 Transfer of Ub from E2 to substrate and release of E2
R-HSA-983168 Antigen processing: Ubiquitination & Proteasome degradation
R-HSA-983169 Class I MHC mediated antigen processing & presentation
R-HSA-1280218 Adaptive Immune System
R-HSA-168256 Immune System

-  Other Names for This Gene
  Alternate Gene Symbols: A3KCU9, ENST00000341084.1, ENST00000341084.2, ENST00000341084.3, ENST00000341084.4, ENST00000341084.5, ENST00000341084.6, NM_183419, Q52LG1, Q9H5H9, Q9H8M8, Q9NV58, Q9UFG0, Q9UFX6, Q9Y4Y1, RN19A_HUMAN, RNF19, uc317vxi.1, uc317vxi.2
UCSC ID: ENST00000341084.7_7
RefSeq Accession: NM_183419.4
Protein: Q9NV58 (aka RN19A_HUMAN)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.