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Summary Expression Phenotypes Gene Literature (2) GO Terms (44) Nucleotides (170) Proteins (36) Interactants (131) Wiki
XB-GENEPAGE-6035626
???displayGene.symbol???:
 ash1l

???displayGene.name???: 
ash1 (absent, small, or homeotic)-like

???displayGene.synonyms???
LOC108699167 , LOC108700623 ( Nomenclature history )

???displayGene.geneFunction???
transcription factor

AI Protein Function :
The gene ash1l encodes a histone-lysine n-methyltransferase, a transcription factor with a set domain that methylates histone h3 on lysine 36 (h3k36me). It is localized to the nucleus. Its function is ...[+]


InterPro :
AT hook DNA-bd motif, AWS dom, BAH dom, BAH sf, [+]

???displayGene.geneInteractants???
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Diseases: 


Disease Ontology:
autosomal dominant intellectual developmental disorder 52

MIM:
INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 52; MRD52

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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