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    ABHD11 abhydrolase domain containing 11 [ Homo sapiens (human) ]

    Gene ID: 83451, updated on 27-Dec-2024

    Summary

    Official Symbol
    ABHD11provided by HGNC
    Official Full Name
    abhydrolase domain containing 11provided by HGNC
    Primary source
    HGNC:HGNC:16407
    See related
    Ensembl:ENSG00000106077 MIM:621050; AllianceGenome:HGNC:16407
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    PP1226; WBSCR21
    Summary
    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]
    Expression
    Ubiquitous expression in colon (RPKM 10.9), thyroid (RPKM 9.6) and 25 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See ABHD11 in Genome Data Viewer
    Location:
    7q11.23
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (73736094..73738802, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (74936993..74939701, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (73150424..73153132, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 8580 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26129 Neighboring gene RNA, 7SL, cytoplasmic 265, pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:73152931-73153588 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:73153589-73154245 Neighboring gene BICD family like 3, pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:73156848-73158047 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73175993-73176570 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73176571-73177148 Neighboring gene claudin 3 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:73213712-73214352 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18267 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:73234209-73234787 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr7:73236582-73237781 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73241685-73242332 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73242333-73242980 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73245012-73245714 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73245715-73246417 Neighboring gene claudin 4

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables carboxylic ester hydrolase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables lipase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in lipid metabolic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    located_in mitochondrial matrix IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in mitochondrion HTP PubMed 
    is_active_in mitochondrion IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in mitochondrion IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of oxoglutarate dehydrogenase complex IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    sn-1-specific diacylglycerol lipase ABHD11
    Names
    Williams Beuren syndrome chromosome region 21
    abhydrolase domain-containing protein 11
    alpha/beta hydrolase domain-containing protein 11
    protein ABHD11
    NP_001138836.2
    NP_001287987.2
    NP_683710.2
    NP_683711.2
    XP_024302716.1
    XP_024302717.2
    XP_047276840.1
    XP_047276841.1
    XP_047276842.1
    XP_054215090.1
    XP_054215091.1
    XP_054215092.1
    XP_054215093.1
    XP_054215094.1

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_001145364.3NP_001138836.2  sn-1-specific diacylglycerol lipase ABHD11 isoform 8

      Status: REVIEWED

      Description
      Transcript Variant: This variant (8) lacks a coding exon, compared to variant 1, resulting in a shorter protein (isoform 8).
      Source sequence(s)
      AC073846
      Consensus CDS
      CCDS47607.2
      Related
      ENSP00000378579.5, ENST00000395147.9
      Conserved Domains (1) summary
      PRK10673
      Location:44248
      PRK10673; esterase
    2. NM_001301058.2NP_001287987.2  sn-1-specific diacylglycerol lipase ABHD11 isoform 9

      Status: REVIEWED

      Description
      Transcript Variant: This variant (9) lacks two exons in the central coding region, which results in a frameshift, compared to variant 1. The encoded isoform (9) has a shorter and distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AC073846
      Consensus CDS
      CCDS75615.2
      UniProtKB/TrEMBL
      C9J7Q4
      Related
      ENSP00000397666.2, ENST00000458339.6
      Conserved Domains (1) summary
      PRK10673
      Location:44141
      PRK10673; esterase
    3. NM_148912.4NP_683710.2  sn-1-specific diacylglycerol lipase ABHD11 isoform 1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1, also known as A) encodes isoform 1.
      Source sequence(s)
      AC073846
      Consensus CDS
      CCDS5558.2
      UniProtKB/Swiss-Prot
      H7BYM8, Q6PJU0, Q8N722, Q8N723, Q8NFV2, Q8NFV3, Q8NFV4, Q9HBS8
      Related
      ENSP00000222800.4, ENST00000222800.8
      Conserved Domains (1) summary
      PRK10673
      Location:44305
      PRK10673; esterase
    4. NM_148913.4NP_683711.2  sn-1-specific diacylglycerol lipase ABHD11 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2, also known as D) lacks an alternate in-frame segment, compared to variant 1, resulting in a shorter isoform (2) than isoform 1.
      Source sequence(s)
      AC073846
      Consensus CDS
      CCDS47608.2
      Related
      ENSP00000416970.3, ENST00000437775.7
      Conserved Domains (1) summary
      PRK10673
      Location:53298
      PRK10673; esterase

    RNA

    1. NR_135627.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AC073846
    2. NR_169872.1 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AC073846
      Related
      ENST00000357419.9

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      73736094..73738802 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047420884.1XP_047276840.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X1

    2. XM_024446949.2XP_024302717.2  sn-1-specific diacylglycerol lipase ABHD11 isoform X1

    3. XM_024446948.2XP_024302716.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X2

      Conserved Domains (1) summary
      cl26326
      Location:130347
      PRK10673; acyl-CoA esterase; Provisional
    4. XM_047420886.1XP_047276842.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X4

    5. XM_047420885.1XP_047276841.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X3

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      74936993..74939701 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054359117.1XP_054215092.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X1

    2. XM_054359115.1XP_054215090.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X1

    3. XM_054359116.1XP_054215091.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X2

    4. XM_054359119.1XP_054215094.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X4

    5. XM_054359118.1XP_054215093.1  sn-1-specific diacylglycerol lipase ABHD11 isoform X3

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001145363.1: Suppressed sequence

      Description
      NM_001145363.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
    2. NM_001321383.1: Suppressed sequence

      Description
      NM_001321383.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.
    3. NM_148914.2: Suppressed sequence

      Description
      NM_148914.2: This RefSeq was permanently suppressed because the transcript represents use of non-consensus splice sites and there is insufficient supporting data.
    4. NM_148916.3: Suppressed sequence

      Description
      NM_148916.3: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
    5. NR_026912.2: Suppressed sequence

      Description
      NR_026912.2: This RefSeq was removed because currently there is insufficient support for the transcript.