Bos taurus Gene: TYROBP
Summary
InnateDB Gene IDBG-636049.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TYROBP
Gene Name TYRO protein tyrosine kinase-binding protein
Synonyms dap12
Species Bos taurus
Ensembl Gene ENSBTAG00000007338
Encoded Proteins
TYRO protein tyrosine kinase-binding protein
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Mus musculus] Tyrobp impairs host defence during pneumococcal pneumonia at the primary site of infection by inhibiting phagocytosis by alveolar macrophages.
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000011600:
This gene encodes a transmembrane signaling polypeptide which contains an immunoreceptor tyrosine-based activation motif (ITAM) in its cytoplasmic domain. The encoded protein may associate with the killer-cell inhibitory receptor (KIR) family of membrane glycoproteins and may act as an activating signal transduction element. This protein may bind zeta-chain (TCR) associated protein kinase 70kDa (ZAP-70) and spleen tyrosine kinase (SYK) and play a role in signal transduction, bone modeling, brain myelination, and inflammation. Mutations within this gene have been associated with polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease. Its putative receptor, triggering receptor expressed on myeloid cells 2 (TREM2), also causes PLOSL. Multiple alternative transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 18:46779848-46782546
Strand Reverse strand
Band
Transcripts
ENSBTAT00000009652 ENSBTAP00000009652
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 9 interaction(s) predicted by orthology.
Predicted by orthology
Total 9 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005515 protein binding
GO:0016301 kinase activity
GO:0042802 identical protein binding
Biological Process
GO:0002281 macrophage activation involved in immune response
GO:0002283 neutrophil activation involved in immune response
GO:0007229 integrin-mediated signaling pathway
GO:0016310 phosphorylation
GO:2001204 regulation of osteoclast development
Cellular Component
GO:0009986 cell surface
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
DAP12 interactions pathway
Immune System pathway
Signal regulatory protein (SIRP) family interactions pathway
Cell-Cell communication pathway
Axon guidance pathway
Other semaphorin interactions pathway
Innate Immune System pathway
DAP12 signaling pathway
Semaphorin interactions pathway
Developmental Biology pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
RANKL pathway
REACTOME
DAP12 signaling pathway
DAP12 interactions pathway
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell pathway
Signal regulatory protein (SIRP) family interactions pathway
Other semaphorin interactions pathway
Developmental Biology pathway
Cell-Cell communication pathway
Semaphorin interactions pathway
Innate Immune System pathway
Axon guidance pathway
Adaptive Immune System pathway
Immune System pathway
Innate Immune System pathway
Immune System pathway
Signal regulatory protein (SIRP) family interactions pathway
Axon guidance pathway
Developmental Biology pathway
Semaphorin interactions pathway
Other semaphorin interactions pathway
Cell-Cell communication pathway
DAP12 interactions pathway
DAP12 signaling pathway
KEGG
Natural killer cell mediated cytotoxicity pathway
Osteoclast differentiation pathway
Natural killer cell mediated cytotoxicity pathway
Osteoclast differentiation pathway
INOH
PID NCI
Cross-References
SwissProt Q95J79
TrEMBL B2BBK0 Q95KU7
UniProt Splice Variant
Entrez Gene 282390
UniGene Bt.8939
RefSeq NM_174627 XM_005218906
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL AJ419227 AJ419230 BC126797 DAAA02046954 EF118674 EF118675 EF118676 EF118677 EF118678 EF118679 EF118680 EF118681 EF118684 EF118685 EF118686 EF118687 EF118688 EF118689 EF118692 EF118693 EF118696 EF118697 EF118698 EF118699 EF118700 EF118702 EF118704 EF118705 EF118706 EF118707 EF118708 EF118711 EF118712 EF118714 EF118715 EF118716 EF118717 EF118718 EF118719 EF118720 EF118721 EF118722 EF118723 EF118724 EF118725 EF118726 EF118727 EF118728 EF118729 EF118730 EF118731 EF118732 EF118734 EF118735
GenPept AAI26798 ABO69943 ABO69944 ABO69945 ABO69946 ABO69947 ABO69948 ABO69949 ABO69950 ABO69953 ABO69954 ABO69955 ABO69956 ABO69957 ABO69958 ABO69961 ABO69962 ABO69965 ABO69966 ABO69967 ABO69968 ABO69969 ABO69971 ABO69973 ABO69974 ABO69975 ABO69976 ABO69977 ABO69980 ABO69981 ABO69983 ABO69984 ABO69985 ABO69986 ABO69987 ABO69988 ABO69989 ABO69990 ABO69991 ABO69992 ABO69993 ABO69994 ABO69995 ABO69996 ABO69997 ABO69998 ABO69999 ABO70000 ABO70001 ABO70003 ABO70004 CAD11669 CAD11672
RNA Seq Atlas 282390