Human Gene LYL1 (ENST00000264824.5_7) from GENCODE V47lift37
  Description: LYL1 basic helix-loop-helix family member (from RefSeq NM_005583.5)
Gencode Transcript: ENST00000264824.5_7
Gencode Gene: ENSG00000104903.5_9
Transcript (Including UTRs)
   Position: hg19 chr19:13,209,847-13,213,672 Size: 3,826 Total Exon Count: 4 Strand: -
Coding Region
   Position: hg19 chr19:13,210,133-13,211,985 Size: 1,853 Coding Exon Count: 3 

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 (chr19:13,209,847-13,213,672)mRNA (may differ from genome)Protein (280 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
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HGNCMalacardsMGIOMIMPubMedUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: LYL1_HUMAN
DESCRIPTION: RecName: Full=Protein lyl-1; AltName: Full=Class A basic helix-loop-helix protein 18; Short=bHLHa18; AltName: Full=Lymphoblastic leukemia-derived sequence 1;
SUBUNIT: Efficient DNA binding requires dimerization with another bHLH protein.
SUBCELLULAR LOCATION: Nucleus (Potential).
DISEASE: Note=A chromosomal aberration involving LYL1 may be a cause of a form of T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(7;19)(q35;p13) with TCRB.
SIMILARITY: Contains 1 bHLH (basic helix-loop-helix) domain.
SEQUENCE CAUTION: Sequence=AAA88084.1; Type=Erroneous initiation; Sequence=AAA88085.1; Type=Erroneous initiation; Sequence=AAA92488.1; Type=Erroneous initiation;
WEB RESOURCE: Name=Atlas of Genetics and Cytogenetics in Oncology and Haematology; URL="http://atlasgeneticsoncology.org/Genes/LYL1ID51ch19p13.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: LYL1
Diseases sorted by gene-association score: lymphoblastic leukemia (40), leukemia (16), leukemia, acute lymphoblastic (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: 50.67 RPKM in Whole Blood
Total median expression: 235.43 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 -171.60352-0.488 Picture PostScript Text
3' UTR -113.50286-0.397 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
IPR011598 - HLH_dom

Pfam Domains:
PF00010 - Helix-loop-helix DNA-binding domain

SCOP Domains:
47459 - HLH, helix-loop-helix DNA-binding domain

ModBase Predicted Comparative 3D Structure on P12980
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 DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000977 RNA polymerase II regulatory region sequence-specific DNA binding
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
GO:0003677 DNA binding
GO:0005515 protein binding
GO:0046983 protein dimerization activity

Biological Process:
GO:0001955 blood vessel maturation
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0030183 B cell differentiation
GO:0045893 positive regulation of transcription, DNA-templated
GO:0060216 definitive hemopoiesis

Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  M22637 - Human LYL-1 protein mRNA, complete cds.
BC002796 - Homo sapiens lymphoblastic leukemia derived sequence 1, mRNA (cDNA clone MGC:3943 IMAGE:3619444), complete cds.
JD078733 - Sequence 59757 from Patent EP1572962.
JD184804 - Sequence 165828 from Patent EP1572962.
JD513432 - Sequence 494456 from Patent EP1572962.
JD324973 - Sequence 305997 from Patent EP1572962.
JD394538 - Sequence 375562 from Patent EP1572962.
AB463845 - Synthetic construct DNA, clone: pF1KB7572, Homo sapiens LYL1 gene for lymphoblastic leukemia derived sequence 1, without stop codon, in Flexi system.
JD035264 - Sequence 16288 from Patent EP1572962.
JD025069 - Sequence 6093 from Patent EP1572962.
LF212212 - JP 2014500723-A/19715: Polycomb-Associated Non-Coding RNAs.
AK311530 - Homo sapiens cDNA, FLJ18572.
JD483071 - Sequence 464095 from Patent EP1572962.
JD343557 - Sequence 324581 from Patent EP1572962.
JD057794 - Sequence 38818 from Patent EP1572962.
JD103477 - Sequence 84501 from Patent EP1572962.
JD401040 - Sequence 382064 from Patent EP1572962.
JD434347 - Sequence 415371 from Patent EP1572962.
JD128632 - Sequence 109656 from Patent EP1572962.
JD393891 - Sequence 374915 from Patent EP1572962.
JD056781 - Sequence 37805 from Patent EP1572962.
MA447789 - JP 2018138019-A/19715: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: BHLHA18, ENST00000264824.1, ENST00000264824.2, ENST00000264824.3, ENST00000264824.4, LYL1_HUMAN, NM_005583, O76102, P12980, uc317hvu.1, uc317hvu.2
UCSC ID: ENST00000264824.5_7
RefSeq Accession: NM_005583.5
Protein: P12980 (aka LYL1_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.