Homo sapiens Protein: WHSC1L1
Summary
InnateDB Protein IDBP-17580.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WHSC1L1
Protein Name Wolf-Hirschhorn syndrome candidate 1-like 1
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000313410
InnateDB Gene IDBG-17572 (WHSC1L1)
Protein Structure
UniProt Annotation
Function Histone methyltransferase. Preferentially methylates 'Lys-4' and 'Lys-27' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation, while 'Lys-27' is a mark for transcriptional repression. {ECO:0000269PubMed:16682010}.
Subcellular Localization Nucleus {ECO:0000250}. Chromosome {ECO:0000250}.
Disease Associations Note=Defects in WHSC1L1 may be involved in non small cell lung carcinomas (NSCLC). Amplified or overexpressed in NSCLC.Note=A chromosomal aberration involving WHSC1L1 is found in childhood acute myeloid leukemia. Translocation t(8;11)(p11.2;p15) with NUP98.
Tissue Specificity Highly expressed in brain, heart and skeletal muscle. Expressed at lower level in liver and lung. {ECO:0000269PubMed:11374904}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 36 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 36 [view]
Protein-Protein 36 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0018024 histone-lysine N-methyltransferase activity
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0016571 histone methylation
GO:0034968 histone lysine methylation
Cellular Component
GO:0005634 nucleus
GO:0005694 chromosome
Protein Structure and Domains
PDB ID
InterPro IPR000313 PWWP domain
PFAM PF00855
PRINTS
PIRSF
SMART SM00293
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9BZ95
PhosphoSite PhosphoSite-Q9BZ95
TrEMBL E9PQ95
UniProt Splice Variant
Entrez Gene 54904
UniGene Hs.722308
RefSeq NP_060248
HUGO HGNC:12767
OMIM 607083
CCDS CCDS6105
HPRD 06155
IMGT
EMBL AC087362 AC087623 AF255649 AF332468 AF332469 AJ295990 AJ295991 AJ295992 AK000360 AK022560 AK127594 BC012059 BC062631 BC101717 BC107734 BC113469 BC115006 BC143510 CH471080
GenPept AAG44637 AAH12059 AAH62631 AAI01718 AAI07735 AAI13470 AAI15007 AAI43511 AAK00354 AAK00355 BAA91110 BAB14099 CAC28350 CAC28351 CAC28352 EAW63320 EAW63321