Gene

Abhd17b

Species
Mus musculus
Symbol
Abhd17b
Name
abhydrolase domain containing 17B
Synonyms
  • 5730446C15Rik
  • Cgi67l
Biotype
protein coding gene
Automated Description
Enables palmitoyl-(protein) hydrolase activity. Involved in protein depalmitoylation; regulation of dendritic spine maintenance; and regulation of protein localization. Located in plasma membrane; postsynaptic density; and recycling endosome membrane. Orthologous to human ABHD17B (abhydrolase domain containing 17B, depalmitoylase).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR12277
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensABHD17B10 of 10YesYes  
Rattus norvegicusAbhd17b9 of 9YesYes   
Xenopus tropicalisabhd17b9 of 9YesYes   
Danio rerioabhd17b1 of 10YesYes  
Drosophila melanogasterCG330967 of 9YesNo   
Caenorhabditis elegansaho-38 of 9YesNo   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
Abhd17a130586747 of 9 
Abhd17c231283727 of 9 
Abhd12334937233 of 9 
Abhd12b430240243 of 9 
Abhd16b530137233 of 9 
Abhd13623147283 of 9 
Abhd16a724338213 of 9 

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
Phenotype Term
Annotation details
References
abnormal cornea morphology
abnormal retina morphology
decreased thigmotaxis
mydriasis
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Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

No mapped variant information available
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
Abhd17bem1(IMPC)J
  • Abhd17bem1J
allele
Yes
Abhd17bem2Gpt
  • Abhd17bem1Cd
allele
Abhd17bGt(OST230394)Lex
  • Fam108bGt(neo)88Lex
allele
Abhd17bem1Gpt
  • Abhd17bem1Cflox
allele
NC_000085.7:g.21657434C>Avariant
SNP
  • intron variant
NC_000085.7:g.21651908C>Gvariant
SNP
  • intron variant
NC_000085.7:g.21651469A>Cvariant
SNP
  • intron variant
NC_000085.7:g.21651950C>Tvariant
SNP
  • intron variant
NC_000085.7:g.21651511G>Avariant
SNP
  • intron variant
NC_000085.7:g.21654213C>Tvariant
SNP
  • intron variant
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Transgenic Alleles

No data available

Models

Model name
Experimental condition
Associated Human Diseases
Associated Phenotypes
Modifier
Source
Abhd17bem1(IMPC)J/Abhd17bem1(IMPC)J [background:] C57BL/6NJ-Abhd17bem1(IMPC)J/J
  • abnormal cornea morphology
  • abnormal retina morphology
MGI
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Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
21.635M21.640M21.645M21.650M21.655M21.660M

Sequence Details

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Expression

Primary Sources
None
Other Sources
Must provide at least one subject
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

No data available