Homo sapiens Protein: LYL1
Summary
InnateDB Protein IDBP-31745.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LYL1
Protein Name lymphoblastic leukemia derived sequence 1
Synonyms bHLHa18;
Species Homo sapiens
Ensembl Protein ENSP00000264824
InnateDB Gene IDBG-31743 (LYL1)
Protein Structure
UniProt Annotation
Function
Subcellular Localization Nucleus {ECO:0000255PROSITE- ProRule:PRU00981}.
Disease Associations 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.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 89 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Experimentally validated
Total 89 [view]
Protein-Protein 11 [view]
Protein-DNA 78 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
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:0030183 B cell differentiation
GO:0045893 positive regulation of transcription, DNA-templated
GO:0060216 definitive hemopoiesis
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR011598 Myc-type, basic helix-loop-helix (bHLH) domain
PFAM PF00010
PRINTS
PIRSF
SMART SM00353
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P12980
PhosphoSite PhosphoSite-P12980
TrEMBL K7ER61
UniProt Splice Variant
Entrez Gene 4066
UniGene Hs.46446
RefSeq NP_005574
HUGO HGNC:6734
OMIM 151440
CCDS CCDS12292
HPRD 01046
IMGT
EMBL AC005546 AC007787 BC002796 M22637 M22638
GenPept AAA88084 AAA88085 AAA92488 AAC33149 AAH02796