Human Gene NDUFA13 (ENST00000507754.9_4) from GENCODE V47lift37
  Description: NADH:ubiquinone oxidoreductase subunit A13 (from RefSeq NM_015965.7)
Gencode Transcript: ENST00000507754.9_4
Gencode Gene: ENSG00000186010.19_8
Transcript (Including UTRs)
   Position: hg19 chr19:19,627,034-19,639,007 Size: 11,974 Total Exon Count: 5 Strand: +
Coding Region
   Position: hg19 chr19:19,627,048-19,638,935 Size: 11,888 Coding Exon Count: 5 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr19:19,627,034-19,639,007)mRNA (may differ from genome)Protein (144 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
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UniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: NDUAD_HUMAN
DESCRIPTION: RecName: Full=NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13; AltName: Full=Cell death regulatory protein GRIM-19; AltName: Full=Complex I-B16.6; Short=CI-B16.6; AltName: Full=Gene associated with retinoic and interferon-induced mortality 19 protein; Short=GRIM-19; Short=Gene associated with retinoic and IFN-induced mortality 19 protein; AltName: Full=NADH-ubiquinone oxidoreductase B16.6 subunit;
FUNCTION: Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Involved in the interferon/all-trans-retinoic acid (IFN/RA) induced cell death. This apoptotic activity is inhibited by interaction with viral IRF1. Prevents the transactivation of STAT3 target genes. May play a role in CARD15-mediated innate mucosal responses and serve to regulate intestinal epithelial cell responses to microbes.
SUBUNIT: Complex I is composed of 45 different subunits. Interacts with CARD15, but not with CARD4. Interacts with STAT3, but not with STAT1, STAT2 and STAT5A. Interacts with HHV-8 IRF1, in the nucleus, with HPV-16 E6 and SV40 LT. Interacts with OLFM4.
INTERACTION: O43464:HTRA2; NbExp=6; IntAct=EBI-372742, EBI-517086;
SUBCELLULAR LOCATION: Mitochondrion inner membrane; Single-pass membrane protein; Matrix side. Nucleus. Note=May be translocated into the nucleus upon IFN/RA treatment.
TISSUE SPECIFICITY: Widely expressed, with highest expression in heart, skeletal muscle, liver, kidney and placenta. In intestinal mucosa, down-regulated in areas involved in Crohn disease and ulcerative colitis.
DEVELOPMENTAL STAGE: Expressed in numerous fetal tissues.
INDUCTION: By IFNB1/IFN-beta combined with all-trans-retinoic acid (ATRA).
DISEASE: Defects in NDUFA13 may be a cause of susceptibility to Hurthle cell thyroid carcinoma (HCTC) [MIM:607464]. Hurthle cell thyroid carcinoma accounts for approximately 3% of all thyroid cancers. Although they are classified as variants of follicular neoplasms, they are more often multifocal and somewhat more aggressive and are less likely to take up iodine than are other follicular neoplasms.
SIMILARITY: Belongs to the complex I NDUFA13 subunit family.
SEQUENCE CAUTION: Sequence=AAD27748.1; Type=Erroneous initiation; Sequence=AAG44670.1; Type=Erroneous initiation; Sequence=AAH00589.2; 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.
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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: NDUFA13
Diseases sorted by gene-association score: thyroid carcinoma, hurthle cell* (950), differentiated thyroid carcinoma* (157), mitochondrial complex i deficiency* (80), leigh syndrome with leukodystrophy* (75), crohn's disease (4)
* = Manually curated disease association

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

+  Common Gene Haplotype Alleles
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+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
3' UTR -16.3072-0.226 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
IPR009346 - GRIM-19

Pfam Domains:
PF06212 - GRIM-19 protein

ModBase Predicted Comparative 3D Structure on Q9P0J0
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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 DetailsGene Details 
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 RGDEnsembl WormBase 
    Protein Sequence 
    Alignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0003954 NADH dehydrogenase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0008137 NADH dehydrogenase (ubiquinone) activity

Biological Process:
GO:0006915 apoptotic process
GO:0010952 positive regulation of peptidase activity
GO:0030308 negative regulation of cell growth
GO:0032981 mitochondrial respiratory chain complex I assembly
GO:0035458 cellular response to interferon-beta
GO:0043280 positive regulation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0045039 protein import into mitochondrial inner membrane
GO:0045732 positive regulation of protein catabolic process
GO:0045892 negative regulation of transcription, DNA-templated
GO:0055114 oxidation-reduction process
GO:0071300 cellular response to retinoic acid
GO:0072593 reactive oxygen species metabolic process
GO:0097190 apoptotic signaling pathway
GO:0097191 extrinsic apoptotic signaling pathway
GO:2001243 negative regulation of intrinsic apoptotic signaling pathway

Cellular Component:
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005746 mitochondrial respiratory chain
GO:0005747 mitochondrial respiratory chain complex I
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0031966 mitochondrial membrane
GO:0070469 respiratory chain


-  Descriptions from all associated GenBank mRNAs
  AF261134 - Homo sapiens CDA016 mRNA, complete cds.
AB528693 - Synthetic construct DNA, clone: pF1KB6924, Homo sapiens NDUFA13 gene for NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13, without stop codon, in Flexi system.
BC009189 - Homo sapiens NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13, mRNA (cDNA clone MGC:15163 IMAGE:3957082), complete cds.
AK298891 - Homo sapiens cDNA FLJ58045 complete cds, highly similar to NADH dehydrogenase (ubiquinone) 1 alpha subcomplex subunit 13 (EC 1.6.5.3).
AK293859 - Homo sapiens cDNA FLJ57958 complete cds, highly similar to NADH dehydrogenase (ubiquinone) 1 alpha subcomplex subunit 13 (EC 1.6.5.3).
AK293965 - Homo sapiens cDNA FLJ59191 complete cds, highly similar to NADH dehydrogenase (ubiquinone) 1 alpha subcomplex subunit 13 (EC 1.6.5.3).
BC000589 - Homo sapiens NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13, mRNA (cDNA clone IMAGE:3346444), partial cds.
AF286697 - Homo sapiens novel cell death-regulatory protein GRIM19 (GRIM19) mRNA, complete cds.
AF155662 - Homo sapiens putative 16.7 kDa protein mRNA, complete cds.
KJ893803 - Synthetic construct Homo sapiens clone ccsbBroadEn_03197 NDUFA13 gene, encodes complete protein.
KR710367 - Synthetic construct Homo sapiens clone CCSBHm_00011956 NDUFA13 (NDUFA13) mRNA, encodes complete protein.
AF132973 - Homo sapiens CGI-39 protein mRNA, complete cds.
CQ903807 - Sequence 9 from Patent WO2004094661.

-  Biochemical and Signaling Pathways
  BioCyc Knowledge Library
PWY-3781 - aerobic respiration I (cytochrome c)

Reactome (by CSHL, EBI, and GO)

Protein Q9P0J0 (Reactome details) participates in the following event(s):

R-HSA-6799178 Intermediate 1 binds HP subcomplex to form Intermediate 2
R-HSA-6799191 Intermediate 2 binds MT-ND1:NDUFAF5:NDUFAF6 to form a 315kDa subcomplex
R-HSA-6799202 The 315kDa subcomplex binds the 370kDa subcomplex to form the 550kDa complex
R-HSA-6799197 ND4, ND5 bind the 550kDa complex to form the 815kDa complex
R-HSA-6799179 Peripheral arm subunits bind the 815kDa complex to form a 980kDa complex
R-HSA-6799196 The MCIA complex, NDUFAF2-7 all dissociate from the 980kDa complex, resulting in Complex I
R-HSA-163217 Complex I oxidises NADH to NAD+, reduces CoQ to QH2
R-HSA-6799198 Complex I biogenesis
R-HSA-611105 Respiratory electron transport
R-HSA-163200 Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
R-HSA-1428517 The citric acid (TCA) cycle and respiratory electron transport
R-HSA-1430728 Metabolism

-  Other Names for This Gene
  Alternate Gene Symbols: B4DF76, CDA016, CGI-39, ENST00000507754.1, ENST00000507754.2, ENST00000507754.3, ENST00000507754.4, ENST00000507754.5, ENST00000507754.6, ENST00000507754.7, ENST00000507754.8, GRIM19, K7EK58, NDUAD_HUMAN, NM_015965, Q6PKI0, Q9H2L3, Q9P0J0, Q9Y327, uc323cup.1, uc323cup.2
UCSC ID: ENST00000507754.9_4
RefSeq Accession: NM_015965.7
Protein: Q9P0J0 (aka NDUAD_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.