Mus musculus Gene: Pafah1b1
Summary
InnateDB Gene IDBG-198862.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pafah1b1
Gene Name platelet-activating factor acetylhydrolase, isoform 1b, subunit 1
Synonyms LIS-1; Lis1; Mdsh; MMS10-U; Ms10u; Pafaha
Species Mus musculus
Ensembl Gene ENSMUSG00000020745
Encoded Proteins
platelet-activating factor acetylhydrolase, isoform 1b, subunit 1
platelet-activating factor acetylhydrolase, isoform 1b, subunit 1
platelet-activating factor acetylhydrolase, isoform 1b, subunit 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000007168:
This locus was identified as encoding a gene that when mutated or lost caused the lissencephaly associated with Miller-Dieker lissencephaly syndrome. This gene encodes the non-catalytic alpha subunit of the intracellular Ib isoform of platelet-activating factor acteylhydrolase, a heterotrimeric enzyme that specifically catalyzes the removal of the acetyl group at the SN-2 position of platelet-activating factor (identified as 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine). Two other isoforms of intracellular platelet-activating factor acetylhydrolase exist: one composed of multiple subunits, the other, a single subunit. In addition, a single-subunit isoform of this enzyme is found in serum. [provided by RefSeq, Apr 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:74673949-74724670
Strand Reverse strand
Band B5
Transcripts
ENSMUST00000102520 ENSMUSP00000099578
ENSMUST00000021091 ENSMUSP00000021091
ENSMUST00000126341
ENSMUST00000156794
ENSMUST00000155493 ENSMUSP00000118231
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 33 experimentally validated interaction(s) in this database.
They are also associated with 31 interaction(s) predicted by orthology.
Experimentally validated
Total 33 [view]
Protein-Protein 32 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 31 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008017 microtubule binding
GO:0032403 protein complex binding
GO:0042803 protein homodimerization activity
GO:0045502 dynein binding
GO:0045505 dynein intermediate chain binding
GO:0051219 phosphoprotein binding
Biological Process
GO:0000132 establishment of mitotic spindle orientation
GO:0000226 microtubule cytoskeleton organization
GO:0001667 ameboidal cell migration
GO:0001675 acrosome assembly
GO:0001764 neuron migration
GO:0001961 positive regulation of cytokine-mediated signaling pathway
GO:0007017 microtubule-based process
GO:0007067 mitotic nuclear division
GO:0007097 nuclear migration
GO:0007268 synaptic transmission
GO:0007405 neuroblast proliferation
GO:0007420 brain development
GO:0007611 learning or memory
GO:0008090 retrograde axon cargo transport
GO:0008344 adult locomotory behavior
GO:0009306 protein secretion
GO:0010977 negative regulation of neuron projection development
GO:0016042 lipid catabolic process
GO:0016477 cell migration
GO:0017145 stem cell division
GO:0019226 transmission of nerve impulse
GO:0021540 corpus callosum morphogenesis
GO:0021766 hippocampus development
GO:0021819 layer formation in cerebral cortex
GO:0021895 cerebral cortex neuron differentiation
GO:0021987 cerebral cortex development
GO:0030036 actin cytoskeleton organization
GO:0031023 microtubule organizing center organization
GO:0032319 regulation of Rho GTPase activity
GO:0036035 osteoclast development
GO:0045773 positive regulation of axon extension
GO:0045931 positive regulation of mitotic cell cycle
GO:0046329 negative regulation of JNK cascade
GO:0047496 vesicle transport along microtubule
GO:0048854 brain morphogenesis
GO:0050885 neuromuscular process controlling balance
GO:0051081 nuclear envelope disassembly
GO:0051660 establishment of centrosome localization
Cellular Component
GO:0000235 astral microtubule
GO:0000776 kinetochore
GO:0005635 nuclear envelope
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005829 cytosol
GO:0005871 kinesin complex
GO:0005875 microtubule associated complex
GO:0005938 cell cortex
GO:0015630 microtubule cytoskeleton
GO:0030424 axon
GO:0030426 growth cone
GO:0031252 cell leading edge
GO:0031512 motile primary cilium
GO:0031965 nuclear membrane
GO:0031982 vesicle
GO:0043005 neuron projection
GO:0043025 neuronal cell body
GO:0048471 perinuclear region of cytoplasm
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Recruitment of mitotic centrosome proteins and complexes pathway
G2/M Transition pathway
Cell Cycle, Mitotic pathway
Separation of Sister Chromatids pathway
Resolution of Sister Chromatid Cohesion pathway
Loss of Nlp from mitotic centrosomes pathway
Cell Cycle pathway
M Phase pathway
Mitotic G2-G2/M phases pathway
Loss of proteins required for interphase microtubule organization� from the centrosome pathway
Mitotic Metaphase and Anaphase pathway
Mitotic Prometaphase pathway
Regulation of PLK1 Activity at G2/M Transition pathway
Mitotic Anaphase pathway
Centrosome maturation pathway
KEGG
Ether lipid metabolism pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Resolution of Sister Chromatid Cohesion pathway
Mitotic Prometaphase pathway
Separation of Sister Chromatids pathway
Regulation of PLK1 Activity at G2/M Transition pathway
Loss of Nlp from mitotic centrosomes pathway
Loss of proteins required for interphase microtubule organization� from the centrosome pathway
Recruitment of mitotic centrosome proteins and complexes pathway
Cell Cycle pathway
M Phase pathway
Mitotic Anaphase pathway
Centrosome maturation pathway
G2/M Transition pathway
Cell Cycle, Mitotic pathway
Mitotic G2-G2/M phases pathway
Mitotic Metaphase and Anaphase pathway
KEGG
Ether lipid metabolism pathway
INOH
PID NCI
Reelin signaling pathway
Lissencephaly gene (LIS1) in neuronal migration and development
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.396952 Mm.397111 Mm.399647 Mm.409385 Mm.473922
RefSeq NM_013625
OMIM
CCDS CCDS25035
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas