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Gene : ABHD11 Homo sapiens

Name  ? abhydrolase domain containing 11 Cytological Location  7q11.23
Brief Description  abhydrolase domain containing 11
Description  This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]
  • synonyms:
  • ABHD11,
  • Williams Beuren syndrome chromosome region 21,
  • AF217971,
  • NM_001145364,
  • WBSCR21,
  • PP1226,
  • OTTHUMG00000130029,
  • HGNC:16407,
  • uc003tzb.4,
  • WBSCR21,
  • PP1226
  • identifiers:
  • 83451,
  • ENSG00000106077,
  • ABHD11

Genome feature

Region: gene ? Length: 2773  
Location: 7:73736094-73738866 reverse strand Cyto location: 7q11.23

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Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

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Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SNPs

4 Cross References

16 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results