Human Gene MYB (uc003qfj.3)
  Description: Homo sapiens v-myb myeloblastosis viral oncogene homolog (avian) (MYB), transcript variant 5, mRNA.
RefSeq Summary (NM_001161657): This gene encodes a protein with three HTH DNA-binding domains that functions as a transcription regulator. This protein plays an essential role in the regulation of hematopoiesis. This gene may be aberrently expressed or rearranged or undergo translocation in leukemias and lymphomas, and is considered to be an oncogene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016].
Transcript (Including UTRs)
   Position: hg19 chr6:135,502,453-135,540,311 Size: 37,859 Total Exon Count: 15 Strand: +


Page IndexSequence and LinksPrimersGenetic AssociationsMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionOther SpeciesmRNA DescriptionsOther NamesModel Information
Methods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr6:135,502,453-135,540,311)mRNA (may differ from genome)No protein
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
BioGPSEnsemblExonPrimerHGNCLynxMalacards
PubMedTreefamWikipedia

-  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


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): MYB
CDC HuGE Published Literature: MYB
Positive Disease Associations: Beta thalassemia/hemoglobin E disease , hematocrit , hematological parameters , mean corpuscular hemoglobin , mean corpuscular volume , other erythrocyte phenotypes
Related Studies:
  1. Beta thalassemia/hemoglobin E disease
    Nuinoon ,et al. 2009, A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E, Human genetics 2009 . [PubMed 19924444]
  2. hematocrit
    Ganesh ,et al. 2009, Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium, Nature genetics 2009 41- 11 : 1191-8. [PubMed 19862010]
  3. hematological parameters
    Soranzo ,et al. 2009, A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium, Nature genetics 2009 41- 11 : 1182-90. [PubMed 19820697]
           more ... click here to view the complete list

-  MalaCards Disease Associations
  MalaCards Gene Search: MYB
Diseases sorted by gene-association score: angiocentric glioma* (260), acute basophilic leukemia* (247), precursor t-cell acute lymphoblastic leukemia* (106), leukemia, acute lymphoblastic* (30), tuberculous salpingitis (15), malignant histiocytosis (12), trachea adenoid cystic carcinoma (10), gallbladder adenocarcinoma (10), tracheal cancer (7), bone ewing's sarcoma (6), myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiency (5), polymorphous low-grade adenocarcinoma (5), leukemia, chronic myeloid, somatic (2), leukemia, acute myeloid (0)
* = Manually curated disease association

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

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 8.02 RPKM in Colon - Transverse
Total median expression: 34.49 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.

-  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
      
      
      
      
      

-  Descriptions from all associated GenBank mRNAs
  AJ606317 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 8A.
AJ606318 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 9Ai.
AJ606319 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 9Aii.
AJ606320 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 8.
AJ606321 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 8B.
AJ606322 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 10A.
AJ606323 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 13A.
AJ606324 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene), splice variant 14A.
FW340095 - Screening.
X52125 - Human alternatively spliced c-myb mRNA (clone=pMbm-1).
BC064955 - Homo sapiens v-myb myeloblastosis viral oncogene homolog (avian), mRNA (cDNA clone MGC:70781 IMAGE:6069320), complete cds.
AJ616235 - Homo sapiens mRNA for v-myb myeloblastosis viral oncogene homologue (avian), (c-myb gene).
M15024 - Human c-myb mRNA, complete cds.
AF104863 - Homo sapiens MYB proto-oncogene protein (MYB) mRNA, complete cds.
AB527731 - Synthetic construct DNA, clone: pF1KB6253, Homo sapiens MYB gene for v-myb myeloblastosis viral oncogene homolog, without stop codon, in Flexi system.
KJ891658 - Synthetic construct Homo sapiens clone ccsbBroadEn_01052 MYB gene, encodes complete protein.
AY787443 - Homo sapiens isolate DelE13 c-myb-like mRNA, complete sequence.
AY787444 - Homo sapiens isolate DelE3E5 c-myb-like mRNA, complete sequence.
AY787445 - Homo sapiens isolate DelE3E8A c-myb-like mRNA, complete sequence.
AY787446 - Homo sapiens isolate DelE5E8A c-myb-like mRNA, complete sequence.
AY787447 - Homo sapiens isolate DelE8 c-myb-like mRNA, complete sequence.
AY787448 - Homo sapiens isolate DelE9 c-myb-like mRNA, complete sequence.
AY787452 - Homo sapiens isolate E12L-2 c-myb-like mRNA, complete sequence.
AY787453 - Homo sapiens isolate E13A c-myb-like mRNA, complete sequence.
AY787454 - Homo sapiens isolate E8A c-myb-like mRNA, complete sequence.
AY787455 - Homo sapiens isolate E8A2E9B c-myb-like mRNA, complete sequence.
AY787459 - Homo sapiens isolate E8SE8A c-myb-like mRNA, complete sequence.
AY787460 - Homo sapiens isolate E8SE8AE9B c-myb-like mRNA, complete sequence.
AY787461 - Homo sapiens isolate E8SE9B c-myb-like mRNA, complete sequence.
AY787462 - Homo sapiens isolate E8SE9S-85E9AB c-myb-like mRNA, complete sequence.
AY787463 - Homo sapiens isolate E8SE9S-85E9B c-myb-like mRNA, complete sequence.
AY787464 - Homo sapiens isolate E9A c-myb-like mRNA, complete sequence.
AY787465 - Homo sapiens isolate E9AB c-myb-like mRNA, complete sequence.
AY787467 - Homo sapiens isolate E9B c-myb-like mRNA, complete sequence.
AY787468 - Homo sapiens isolate E9S-48E9B c-myb-like mRNA, complete sequence.
AY787470 - Homo sapiens isolate E9S-85 c-myb-like mRNA, complete sequence.
AY787472 - Homo sapiens isolate E9S-85E9A c-myb-like mRNA, complete sequence.
AY787473 - Homo sapiens isolate E9S-85E9AB c-myb-like mRNA, complete sequence.
AY787474 - Homo sapiens isolate E9S-85E9B c-myb-like mRNA, complete sequence.
AY787475 - Homo sapiens isolate M15024 c-myb-like mRNA, complete sequence.
AY787451 - Homo sapiens isolate E12L-1 c-myb-like mRNA, complete sequence.
AY787449 - Homo sapiens isolate DelE9E10A c-myb-like mRNA, complete sequence.
AY787450 - Homo sapiens isolate E10A c-myb-like mRNA, complete sequence.
AY787456 - Homo sapiens isolate E8AE10A.txt c-myb-like mRNA, complete sequence.
AY787457 - Homo sapiens isolate E8AE9S-85E10A c-myb-like mRNA, complete sequence.
AY787458 - Homo sapiens isolate E8SE10A c-myb-like mRNA, complete sequence.
AY787466 - Homo sapiens isolate E9AE10A c-myb-like mRNA, complete sequence.
AY787469 - Homo sapiens isolate E9S-48E9BE10A c-myb-like mRNA, complete sequence.
AY787471 - Homo sapiens isolate E9S-85E10A c-myb-like mRNA, complete sequence.
X52126 - Human alternatively spliced c-myb mRNA (clone=pMbm-2).
M13665 - Human c-myb mRNA, 3'end.
BC035996 - Homo sapiens, Similar to v-myb myeloblastosis viral oncogene homolog (avian), clone IMAGE:4686589, mRNA.
AJ616791 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 1 and joined CDS.
JD445418 - Sequence 426442 from Patent EP1572962.
JD173383 - Sequence 154407 from Patent EP1572962.
JD057050 - Sequence 38074 from Patent EP1572962.
AJ616792 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 2.
M13666 - Human c-myb mRNA, 3' end.
AJ616793 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 3.
AJ616794 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 4.
FJ969915 - Homo sapiens MYB/NFIB fusion protein variant 1 (MYB/NFIB fusion) mRNA, partial cds.
FJ969916 - Homo sapiens MYB/NFIB fusion protein variant 2 (MYB/NFIB fusion) mRNA, partial cds.
FJ969917 - Homo sapiens MYB/NFIB fusion protein variant 3 (MYB/NFIB fusion) mRNA, partial cds.
AJ616795 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 5.
AJ616796 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 6.
AJ616797 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 7.
AJ616798 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 8.
X17469 - Human mRNA for c-myb gene exon 9A.
AJ616800 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 10.
AJ616801 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 11.
AJ616802 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 12.
CQ873766 - Sequence 185 from Patent WO2004076622.
DD413603 - Regulation of Mammalian Cells.
AJ616803 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 13.
AJ616804 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 14.
AJ616805 - Homo sapiens c-myb gene for v-myb myeloblastosis viral oncogene homologue (avian), exon 15.
JD545763 - Sequence 526787 from Patent EP1572962.
JD333991 - Sequence 315015 from Patent EP1572962.
FW573307 - JP 2010529847-A/28: Oligonucleotides for modulation of target RNA activity.
HI463868 - Sequence 13 from Patent EP2124967.
JD557793 - Sequence 538817 from Patent EP1572962.
CQ873705 - Sequence 124 from Patent WO2004076622.
DD413542 - Regulation of Mammalian Cells.
HI463869 - Sequence 14 from Patent EP2124967.
HI463870 - Sequence 15 from Patent EP2124967.
FW573305 - JP 2010529847-A/26: Oligonucleotides for modulation of target RNA activity.
FW573306 - JP 2010529847-A/27: Oligonucleotides for modulation of target RNA activity.
HI463871 - Sequence 16 from Patent EP2124967.
HI463872 - Sequence 17 from Patent EP2124967.
FW573308 - JP 2010529847-A/29: Oligonucleotides for modulation of target RNA activity.
HI463873 - Sequence 18 from Patent EP2124967.
HI463874 - Sequence 19 from Patent EP2124967.
HI463875 - Sequence 20 from Patent EP2124967.
JD232050 - Sequence 213074 from Patent EP1572962.
HI463876 - Sequence 21 from Patent EP2124967.
HI463877 - Sequence 22 from Patent EP2124967.
JD182305 - Sequence 163329 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: AY787449
UCSC ID: uc003qfj.3
RefSeq Accession: NM_001161657

-  Gene Model Information
 
category: nearCoding nonsense-mediated-decay: yes RNA accession: AY787449.1
exon count: 15CDS single in 3' UTR: no RNA size: 2911
ORF size: 0CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1967.00frame shift in genome: no % Coverage: 100.00
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
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.