Human Gene HOXA9 (ENST00000343483.7_7) from GENCODE V47lift37
  Description: homeobox A9 (from RefSeq NM_152739.4)
Gencode Transcript: ENST00000343483.7_7
Gencode Gene: ENSG00000078399.19_10
Transcript (Including UTRs)
   Position: hg19 chr7:27,202,057-27,205,156 Size: 3,100 Total Exon Count: 2 Strand: -
Coding Region
   Position: hg19 chr7:27,203,222-27,205,076 Size: 1,855 Coding Exon Count: 2 

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

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr7:27,202,057-27,205,156)mRNA (may differ from genome)Protein (272 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: HXA9_HUMAN
DESCRIPTION: RecName: Full=Homeobox protein Hox-A9; AltName: Full=Homeobox protein Hox-1G;
FUNCTION: Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. Required for induction of E-selectin and VCAM-1, on the endothelial cells surface at sites of inflammation.
SUBUNIT: Transiently interacts with PRMT5 in TNF-alpha stimulated endothelial cells.
INTERACTION: Q15654:TRIP6; NbExp=4; IntAct=EBI-742314, EBI-742327;
SUBCELLULAR LOCATION: Nucleus.
PTM: Methylated on Arg-140 by PRMT5; methylation is critical for E-selectin induction.
DISEASE: Note=A chromosomal aberration involving HOXA9 is found in a form of acute myeloid leukemia. Translocation t(7;11)(p15;p15) with NUP98.
DISEASE: Note=A chromosomal aberration involving HOXA9 may contribute to disease progression in chronic myeloid leukemia. Translocation t(7;17)(p15;q23) with MSI2.
SIMILARITY: Belongs to the Abd-B homeobox family.
SIMILARITY: Contains 1 homeobox DNA-binding domain.
SEQUENCE CAUTION: Sequence=AAC50364.1; Type=Erroneous initiation;
WEB RESOURCE: Name=Atlas of Genetics and Cytogenetics in Oncology and Haematology; URL="http://atlasgeneticsoncology.org/Genes/HOXA9.html";

-  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: HOXA9
Diseases sorted by gene-association score: myeloid leukemia (10), myelodysplastic syndrome (3), clivus chordoma (2), leukemia, chronic myeloid, somatic (2), leukemia, acute myeloid (1)

-  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: 1.30 RPKM in Kidney - Cortex
Total median expression: 15.64 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 -24.0080-0.300 Picture PostScript Text
3' UTR -288.701165-0.248 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
IPR017970 - Homeobox_CS
IPR017112 - Homeobox_Hox9
IPR020479 - Homeobox_metazoa
IPR001356 - Homeodomain
IPR009057 - Homeodomain-like
IPR006711 - Hox9_activation_N

Pfam Domains:
PF00046 - Homeodomain
PF04617 - Hox9 activation region

SCOP Domains:
46689 - Homeodomain-like

ModBase Predicted Comparative 3D Structure on P31269
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 orthologNo orthologNo ortholog
Gene Details  Gene Details  
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-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
GO:0003677 DNA binding
GO:0005515 protein binding
GO:0019899 enzyme binding
GO:0043565 sequence-specific DNA binding

Biological Process:
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007275 multicellular organism development
GO:0042118 endothelial cell activation
GO:0045638 negative regulation of myeloid cell differentiation

Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  KJ891379 - Synthetic construct Homo sapiens clone ccsbBroadEn_00773 HOXA9 gene, encodes complete protein.
LF207143 - JP 2014500723-A/14646: Polycomb-Associated Non-Coding RNAs.
BC006537 - Homo sapiens homeobox A9, mRNA (cDNA clone MGC:1934 IMAGE:2987903), complete cds.
BC010023 - Homo sapiens homeobox A9, mRNA (cDNA clone MGC:19648 IMAGE:2987818), complete cds.
U41813 - Human class I homeoprotein (HOXA9) mRNA, partial cds.
JD082958 - Sequence 63982 from Patent EP1572962.
JD312493 - Sequence 293517 from Patent EP1572962.
LF362370 - JP 2014500723-A/169873: Polycomb-Associated Non-Coding RNAs.
JD345926 - Sequence 326950 from Patent EP1572962.
LF362371 - JP 2014500723-A/169874: Polycomb-Associated Non-Coding RNAs.
JD109833 - Sequence 90857 from Patent EP1572962.
JD434644 - Sequence 415668 from Patent EP1572962.
JD359417 - Sequence 340441 from Patent EP1572962.
JD052542 - Sequence 33566 from Patent EP1572962.
JD126499 - Sequence 107523 from Patent EP1572962.
JD520771 - Sequence 501795 from Patent EP1572962.
U82759 - Human homeodomain protein HoxA9 mRNA, complete cds.
JD219204 - Sequence 200228 from Patent EP1572962.
JD302405 - Sequence 283429 from Patent EP1572962.
JD316128 - Sequence 297152 from Patent EP1572962.
JD306241 - Sequence 287265 from Patent EP1572962.
BT006990 - Homo sapiens homeo box A9 mRNA, complete cds.
DQ892748 - Synthetic construct clone IMAGE:100005378; FLH189329.01X; RZPDo839D1274D homeobox A9 (HOXA9) gene, encodes complete protein.
DQ895994 - Synthetic construct Homo sapiens clone IMAGE:100010454; FLH189325.01L; RZPDo839D1264D homeobox A9 (HOXA9) gene, encodes complete protein.
AB463749 - Synthetic construct DNA, clone: pF1KB8338, Homo sapiens HOXA9 gene for homeobox A9, without stop codon, in Flexi system.
AM393527 - Synthetic construct Homo sapiens clone IMAGE:100002159 for hypothetical protein (HOXA9 gene).
JD332581 - Sequence 313605 from Patent EP1572962.
JD175178 - Sequence 156202 from Patent EP1572962.
JD099067 - Sequence 80091 from Patent EP1572962.
DQ655931 - Homo sapiens clone UGL14a03, mRNA sequence.
U41814 - Human NUP98-HOXA9 fusion protein mRNA, partial cds.
LF212033 - JP 2014500723-A/19536: Polycomb-Associated Non-Coding RNAs.
JD119045 - Sequence 100069 from Patent EP1572962.
MA442720 - JP 2018138019-A/14646: Polycomb-Associated Non-Coding RNAs.
MA597947 - JP 2018138019-A/169873: Polycomb-Associated Non-Coding RNAs.
MA597948 - JP 2018138019-A/169874: Polycomb-Associated Non-Coding RNAs.
MA447610 - JP 2018138019-A/19536: Polycomb-Associated Non-Coding RNAs.
MF139050 - Homo sapiens pri-hsa-miRNA 196b variant 1 miRNA gene, partial sequence.
MF139051 - Homo sapiens pri-hsa-miRNA 196b spliced variant 1 miRNA gene, partial sequence.

-  Other Names for This Gene
  Alternate Gene Symbols: ENST00000343483.1, ENST00000343483.2, ENST00000343483.3, ENST00000343483.4, ENST00000343483.5, ENST00000343483.6, HOX1G, HXA9_HUMAN, NM_152739, O43369, O43429, P31269, Q99820, uc317wqt.1, uc317wqt.2
UCSC ID: ENST00000343483.7_7
RefSeq Accession: NM_152739.4
Protein: P31269 (aka HXA9_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.