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Gene : ASXL2 Homo sapiens

Name  ? ASXL transcriptional regulator 2 Cytological Location  2p23.3
Brief Description  ASXL transcriptional regulator 2
Description  This gene encodes a member of a family of epigenetic regulators that bind various histone-modifying enzymes and are involved in the assembly of transcription factors at specific genomic loci. Naturally occurring mutations in this gene are associated with cancer in several tissue types (breast, bladder, pancreas, ovary, prostate, and blood). This gene plays an important role in neurodevelopment, cardiac function, adipogenesis, and osteoclastogenesis. [provided by RefSeq, Feb 2017]
  • synonyms:
  • FLJ10898,
  • additional sex combs like 2 (Drosophila),
  • ASXL2,
  • NM_018263,
  • uc061hgj.1,
  • additional sex combs like 2, transcriptional regulator,
  • ASXH2,
  • OTTHUMG00000152176,
  • HGNC:23805,
  • KIAA1685,
  • ASXH2
  • identifiers:
  • 55252,
  • ENSG00000143970,
  • ASXL2

Genome feature

Region: gene ? Length: 144735  
Location: 2:25733753-25878487 reverse strand Cyto location: 2p23.3

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



481 SNPs

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results