Human Gene HNRNPD (ENST00000313899.12_11) from GENCODE V47lift37
  Description: heterogeneous nuclear ribonucleoprotein D, transcript variant 1 (from RefSeq NM_031370.3)
Gencode Transcript: ENST00000313899.12_11
Gencode Gene: ENSG00000138668.20_20
Transcript (Including UTRs)
   Position: hg19 chr4:83,273,651-83,295,144 Size: 21,494 Total Exon Count: 9 Strand: -
Coding Region
   Position: hg19 chr4:83,276,487-83,294,831 Size: 18,345 Coding Exon Count: 8 

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 (chr4:83,273,651-83,295,144)mRNA (may differ from genome)Protein (355 aa)
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UniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: HNRPD_HUMAN
DESCRIPTION: RecName: Full=Heterogeneous nuclear ribonucleoprotein D0; Short=hnRNP D0; AltName: Full=AU-rich element RNA-binding protein 1;
FUNCTION: Binds with high affinity to RNA molecules that contain AU-rich elements (AREs) found within the 3'-UTR of many proto- oncogenes and cytokine mRNAs. Also binds to double- and single- stranded DNA sequences in a specific manner and functions a transcription factor. Each of the RNA-binding domains specifically can bind solely to a single-stranded non-monotonous 5'-UUAG-3' sequence and also weaker to the single-stranded 5'-TTAGGG-3' telomeric DNA repeat. Binds RNA oligonucleotides with 5'-UUAGGG-3' repeats more tightly than the telomeric single-stranded DNA 5'- TTAGGG-3' repeats. Binding of RRM1 to DNA inhibits the formation of DNA quadruplex structure which may play a role in telomere elongation. May be involved in translationally coupled mRNA turnover. Implicated with other RNA-binding proteins in the cytoplasmic deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of instability (mCRD) domain.
SUBUNIT: Identified in a mRNP granule complex, at least composed of ACTB, ACTN4, DHX9, ERG, HNRNPA1, HNRNPA2B1, HNRNPAB, HNRNPD, HNRNPL, HNRNPR, HNRNPU, HSPA1, HSPA8, IGF2BP1, ILF2, ILF3, NCBP1, NCL, PABPC1, PABPC4, PABPN1, RPLP0, RPS3, RPS3A, RPS4X, RPS8, RPS9, SYNCRIP, TROVE2, YBX1 and untranslated mRNAs. Part of a complex associated with the FOS mCRD domain and consisting of PABPC1, PAIP1, CSDE1/UNR and SYNCRIP. Interacts with IGF2BP2. Interacts with GTPBP1.
INTERACTION: Q04637:EIF4G1; NbExp=3; IntAct=EBI-432545, EBI-73711; Q9Y6M1:IGF2BP2; NbExp=4; IntAct=EBI-432545, EBI-1024419; Q9BYZ2:LDHAL6B; NbExp=2; IntAct=EBI-299674, EBI-1108377; P11940:PABPC1; NbExp=2; IntAct=EBI-432545, EBI-81531; P31947:SFN; NbExp=7; IntAct=EBI-432545, EBI-476295; O60506:SYNCRIP; NbExp=3; IntAct=EBI-432545, EBI-1024357; P67809:YBX1; NbExp=3; IntAct=EBI-432545, EBI-354065;
SUBCELLULAR LOCATION: Nucleus. Cytoplasm. Note=Localized in cytoplasmic mRNP granules containing untranslated mRNAs. Component of ribonucleosomes.
PTM: Arg-345 is dimethylated, probably to asymmetric dimethylarginine.
PTM: Methylated by PRMT1, in an insulin-dependent manner. The PRMT1-mediated methylation regulates tyrosine phosphorylation (By similarity).
SIMILARITY: Contains 2 RRM (RNA recognition motif) domains.
SEQUENCE CAUTION: Sequence=AAA35781.1; Type=Frameshift; Positions=45, 59, 355; Sequence=AAA35781.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Sequence of unknown origin in the N-terminal part; Sequence=CAA27544.1; Type=Miscellaneous discrepancy; Note=Several sequence conflicts;

-  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: HNRNPD
Diseases sorted by gene-association score: chromosome 4q21 deletion syndrome (8)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  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: 96.91 RPKM in Cells - EBV-transformed lymphocytes
Total median expression: 2158.70 RPKM



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

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -142.60313-0.456 Picture PostScript Text
3' UTR -387.201687-0.230 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
IPR012956 - CARG-binding_factor_N
IPR012677 - Nucleotide-bd_a/b_plait
IPR000504 - RRM_dom

Pfam Domains:
PF00076 - RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain)
PF08143 - CBFNT (NUC161) domain
PF16367 - RNA recognition motif

SCOP Domains:
54928 - RNA-binding domain, RBD

Protein Data Bank (PDB) 3-D Structure
MuPIT help
1HD0 - NMR MuPIT 1HD1 - NMR MuPIT 1IQT - NMR MuPIT 1WTB - NMR MuPIT 1X0F - NMR MuPIT 2Z5N - X-ray MuPIT


ModBase Predicted Comparative 3D Structure on Q14103
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-  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 orthologNo orthologNo ortholog
Gene DetailsGene Details    
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-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0003676 nucleic acid binding
GO:0003677 DNA binding
GO:0003680 AT DNA binding
GO:0003682 chromatin binding
GO:0003723 RNA binding
GO:0003729 mRNA binding
GO:0005515 protein binding
GO:0008134 transcription factor binding
GO:0035925 mRNA 3'-UTR AU-rich region binding
GO:0042162 telomeric DNA binding
GO:0042826 histone deacetylase binding

Biological Process:
GO:0000398 mRNA splicing, via spliceosome
GO:0001889 liver development
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006396 RNA processing
GO:0006401 RNA catabolic process
GO:0007420 brain development
GO:0010628 positive regulation of gene expression
GO:0010629 negative regulation of gene expression
GO:0016070 RNA metabolic process
GO:0021549 cerebellum development
GO:0032204 regulation of telomere maintenance
GO:0032355 response to estradiol
GO:0042752 regulation of circadian rhythm
GO:0042789 mRNA transcription from RNA polymerase II promoter
GO:0043488 regulation of mRNA stability
GO:0045727 positive regulation of translation
GO:0045893 positive regulation of transcription, DNA-templated
GO:0048255 mRNA stabilization
GO:0048511 rhythmic process
GO:0051592 response to calcium ion
GO:0051602 response to electrical stimulus
GO:0061158 3'-UTR-mediated mRNA destabilization
GO:0071230 cellular response to amino acid stimulus
GO:0071392 cellular response to estradiol stimulus
GO:0071732 cellular response to nitric oxide
GO:0097167 circadian regulation of translation
GO:1901355 response to rapamycin
GO:1904355 positive regulation of telomere capping
GO:1904383 response to sodium phosphate
GO:1904586 cellular response to putrescine
GO:1905663 positive regulation of telomerase RNA reverse transcriptase activity
GO:1990828 hepatocyte dedifferentiation

Cellular Component:
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:1990904 ribonucleoprotein complex


-  Descriptions from all associated GenBank mRNAs
  KJ891372 - Synthetic construct Homo sapiens clone ccsbBroadEn_00766 HNRNPD gene, encodes complete protein.
KJ905781 - Synthetic construct Homo sapiens clone ccsbBroadEn_15451 HNRNPD gene, encodes complete protein.
AF039575 - Homo sapiens heterogeneous nuclear ribonucleoprotein D0B mRNA, partial cds.
JD094515 - Sequence 75539 from Patent EP1572962.
JD046631 - Sequence 27655 from Patent EP1572962.
JD491402 - Sequence 472426 from Patent EP1572962.
JD025612 - Sequence 6636 from Patent EP1572962.
AL832723 - Homo sapiens mRNA; cDNA DKFZp313H039 (from clone DKFZp313H039).
BC002401 - Homo sapiens heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa), mRNA (cDNA clone MGC:8503 IMAGE:2822230), complete cds.
BC023977 - Homo sapiens heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa), mRNA (cDNA clone MGC:2158 IMAGE:2961272), complete cds.
BC026015 - Homo sapiens heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa), mRNA (cDNA clone MGC:3882 IMAGE:2961272), complete cds.
D55673 - Homo sapiens mRNA for heterogeneous nuclear ribonucleoprotein D (hnRNP D), partial cds, clone cDx8.
D55671 - Homo sapiens mRNA for heterogeneous nuclear ribonucleoprotein D (hnRNP D), partial cds, clone cDx4.
D55674 - Homo sapiens mRNA for heterogeneous nuclear ribonucleoprotein D (hnRNP D), complete cds, clone cDx9.
D55672 - Homo sapiens mRNA for heterogeneous nuclear ribonucleoprotein D (hnRNP D), complete cds, clone cDx7.
JD032977 - Sequence 14001 from Patent EP1572962.
JD080607 - Sequence 61631 from Patent EP1572962.
JD124009 - Sequence 105033 from Patent EP1572962.
JD166843 - Sequence 147867 from Patent EP1572962.
JD350884 - Sequence 331908 from Patent EP1572962.
M94630 - Homo sapiens DNA-binding protein mRNA, complete cds.
AK057836 - Homo sapiens cDNA FLJ25107 fis, clone CBR01496, highly similar to Human mRNA for heterogeneous nuclear ribonucleoprotein D (hnRNP D).
AK300149 - Homo sapiens cDNA FLJ54150 complete cds, highly similar to Heterogeneous nuclear ribonucleoprotein D0.
JD357813 - Sequence 338837 from Patent EP1572962.
AK292707 - Homo sapiens cDNA FLJ76462 complete cds, highly similar to Homo sapiens heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) (HNRPD), transcript variant 2, mRNA.
AK303552 - Homo sapiens cDNA FLJ61020 complete cds, highly similar to Heterogeneous nuclear ribonucleoprotein D0.
JD313690 - Sequence 294714 from Patent EP1572962.
DQ892240 - Synthetic construct clone IMAGE:100004870; FLH184421.01X; RZPDo839F10144D heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) (HNRPD) gene, encodes complete protein.
DQ895440 - Synthetic construct Homo sapiens clone IMAGE:100009900; FLH184417.01L; RZPDo839F10143D heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) (HNRPD) gene, encodes complete protein.
AB463729 - Synthetic construct DNA, clone: pF1KB8275, Homo sapiens HNRPD gene for heterogeneous nuclear ribonucleoprotein D, without stop codon, in Flexi system.
X03910 - Human mRNA for hnRNP C protein cross-reacting with C1 and C2 hnRNP core proteins.
JD462440 - Sequence 443464 from Patent EP1572962.
JD555131 - Sequence 536155 from Patent EP1572962.
JD107060 - Sequence 88084 from Patent EP1572962.
JD404564 - Sequence 385588 from Patent EP1572962.
JD477847 - Sequence 458871 from Patent EP1572962.
JD138132 - Sequence 119156 from Patent EP1572962.

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

Protein Q14103 (Reactome details) participates in the following event(s):

R-HSA-72103 Formation of pre-mRNPs
R-HSA-72107 Formation of the Spliceosomal E complex
R-HSA-72124 Formation of the Spliceosomal A Complex
R-HSA-72127 Formation of the Spliceosomal B Complex
R-HSA-72130 Formation of an intermediate Spliceosomal C (Bact) complex
R-HSA-72143 Lariat Formation and 5'-Splice Site Cleavage
R-HSA-72139 Formation of the active Spliceosomal C (B*) complex
R-HSA-156661 Formation of Exon Junction Complex
R-HSA-72203 Processing of Capped Intron-Containing Pre-mRNA
R-HSA-72163 mRNA Splicing - Major Pathway
R-HSA-8953854 Metabolism of RNA
R-HSA-72172 mRNA Splicing
R-HSA-450434 AUF1(hnRNP D0) dimers bind AU-rich element in 3' UTR of mRNA
R-HSA-450551 AUF1 binds translation and heat shock proteins
R-HSA-450408 AUF1 (hnRNP D0) binds and destabilizes mRNA
R-HSA-450531 Regulation of mRNA stability by proteins that bind AU-rich elements
R-HSA-8953854 Metabolism of RNA
R-HSA-450434 AUF1(hnRNP D0) dimers bind AU-rich element in 3' UTR of mRNA
R-HSA-450551 AUF1 binds translation and heat shock proteins
R-HSA-450408 AUF1 (hnRNP D0) binds and destabilizes mRNA
R-HSA-450531 Regulation of mRNA stability by proteins that bind AU-rich elements
R-HSA-8953854 Metabolism of RNA

-  Other Names for This Gene
  Alternate Gene Symbols: A8K9J2, AUF1, ENST00000313899.1, ENST00000313899.10, ENST00000313899.11, ENST00000313899.2, ENST00000313899.3, ENST00000313899.4, ENST00000313899.5, ENST00000313899.6, ENST00000313899.7, ENST00000313899.8, ENST00000313899.9, HNRPD, HNRPD_HUMAN, NM_031370, P07029, Q01858, Q14100, Q14101, Q14102, Q14103, Q4W5A1, Q9UCE8, Q9UCE9, uc317pmx.1, uc317pmx.2
UCSC ID: ENST00000313899.12_11
RefSeq Accession: NM_031370.3
Protein: Q14103 (aka HNRPD_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.