ABHD11, abhydrolase domain containing 11

ABHD11, abhydrolase domain containing 11

• 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]

• Gene Synonyms (protein ABHD11, Williams Beuren syndrome chromosome region 21, abhydrolase domain-containing protein 11, alpha/beta hydrolase domain-containing protein 11, PP1226, WBSCR21,)
• NCBI Gene ID: 83451
• Species: Homo sapiens (Human)
• UNIPROT ID#>>D3DXF2
  UNIPROT ID#>>C9J7Q4
  UNIPROT ID#>>Q8NFV4
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

abhydrolase domain containing 11 interacts with:

• 4-hydroxy-2-oxoglutarate aldolase 1
  abhydrolase domain containing 11
  alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
  bolA family member 3
  coiled-coil-helix-coiled-coil-helix domain containing 4
  deltex E3 ubiquitin ligase 2
  docking protein 6
  MORN repeat containing 3
  peptidyl-tRNA hydrolase domain containing 1
  proline rich 35
  USH1 protein network component harmonin binding protein 1

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.