Gene: Abhd16a

Order

Name abhydrolase domain containing 16A

Synonyms
  • NG26
  • Bat5
  • D17H6S82E

Status ES CellsMice
tm1a
phenotype data available

Links MGI:99476    Ensembl Gene    Ensembl Orthologs    My Genes   

Viability Homozygous - Subviable

Phenotype associations for Abhd16a

Significant     Not Significant     Not tested    
All Phenotypes Summary

Based on automated MP annotations supported by experiments on knockout mouse models. Click on icons to go to all Abhd16a data for that phenotype.

Significant Phenotypes

System Phenotype Allele Zyg Sex Life Stage P Value Data
male infertility Abhd16atm1a(EUCOMM)Wtsi HOM Male postpartum stage 0.0
preweaning lethality, incomplete penetrance Abhd16atm1a(EUCOMM)Wtsi HOM Female Male n/a 0.0
decreased circulating alanine transaminase level Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 2.01E-7
increased lean body mass Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 6.04E-7
decreased circulating cholesterol level Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 9.64E-7
decreased effector memory CD8-positive, alpha-beta T cell number Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 4.0E-6
decreased circulating insulin level Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 8.23E-6
decreased body length Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 2.07E-5
decreased circulating glucose level Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 2.59E-5
decreased total body fat amount Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 3.56E-5
decreased circulating potassium level Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 6.0E-5
increased bone mineral content Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 7.89E-5
abnormal bone structure Abhd16atm1a(EUCOMM)Wtsi HOM Female Male postnatal 8.77E-5

Download data as: TSV XLS



Expression

Expression data not available

Associated Images

Associated Images
  • DSS Histology
    6 Images
Legacy Phenotype Associated Images
Xray (15)
  • Abhd16atm1a(EUCOMM)Wtsi
    WT, Female, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    WT, Female, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    WT, Female, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    WT, Female, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    WT, Female, WTSI

show all 15 images

Dysmorphology (4)
  • Abhd16atm1a(EUCOMM)Wtsi
    eye, abnormal eye morphology, narrow eye opening, HOM, Female, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    abnormal tail morphology, abnormal tail tip morphology, HOM, Male, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    head, upturned snout, short snout, snout, abnormal snout morphology, HOM, Male, WTSI
  • Abhd16atm1a(EUCOMM)Wtsi
    abnormal coat/hair pigmentation, abnormal ventral coat pigmentation, HOM, Female, WTSI

Disease Models

No associations by disease annotation and gene orthology found.

Order Mouse and ES Cells

Targeting Detail Product Ordering
MGI Allele Allele Type Type Map Seq Vector ES Cell Mouse Tissue Enquiry
Abhd16atm1a(EUCOMM)Wtsi KO first allele (reporter-tagged insertion with conditional potential)
Vector
Gene