Bos taurus Gene: BT.102247 | |||||||||||||
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Summary | |||||||||||||
InnateDB Gene | IDBG-646529.3 | ||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||
Gene Symbol | BT.102247 | ||||||||||||
Gene Name | ras GTPase-activating protein 1 | ||||||||||||
Synonyms | |||||||||||||
Species | Bos taurus | ||||||||||||
Ensembl Gene | ENSBTAG00000009565 | ||||||||||||
Encoded Proteins |
ras GTPase-activating protein 1
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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 ENSG00000145715:
The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues. [provided by RefSeq, May 2012] |
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Gene Information | |||||||||||||
Type | Protein coding | ||||||||||||
Genomic Location | Chromosome 7:89281002-89391377 | ||||||||||||
Strand | Forward strand | ||||||||||||
Band | |||||||||||||
Transcripts |
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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 53 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||
Species
Homo sapiens
Mus musculus
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Gene ID
Gene Order
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Pathway Predictions based on Human Orthology Data | |||||||||||||
NETPATH |
EGFR1 pathway
KitReceptor pathway
TCR pathway
BCR pathway
IL4 pathway
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REACTOME |
Downstream signal transduction pathway
Signaling by PDGF pathway
Developmental Biology pathway
EPHB-mediated forward signaling pathway
Signaling by VEGF pathway
Axon guidance pathway
Signal Transduction pathway
VEGFR2 mediated cell proliferation pathway
VEGFA-VEGFR2 Pathway pathway
EPH-Ephrin signaling pathway
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KEGG |
MAPK signaling pathway pathway
Axon guidance pathway
Axon guidance pathway
MAPK signaling pathway pathway
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INOH |
PDGF signaling pathway pathway
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PID NCI |
Syndecan-2-mediated signaling events
IL2-mediated signaling events
Aurora A signaling
Signaling events mediated by focal adhesion kinase
EPHB forward signaling
Neurotrophic factor-mediated Trk receptor signaling
BCR signaling pathway
Angiopoietin receptor Tie2-mediated signaling
Regulation of Ras family activation
Signaling events regulated by Ret tyrosine kinase
Fc-epsilon receptor I signaling in mast cells
Aurora B signaling
VEGFR1 specific signals
PDGFR-beta signaling pathway
Insulin Pathway
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Cross-References | |||||||||||||
SwissProt | |||||||||||||
TrEMBL | F1N7N8 | ||||||||||||
UniProt Splice Variant | |||||||||||||
Entrez Gene | 282032 | ||||||||||||
UniGene | Bt.102247 | ||||||||||||
RefSeq | NM_174449 | ||||||||||||
HUGO | HGNC:9871 | ||||||||||||
OMIM | |||||||||||||
CCDS | |||||||||||||
HPRD | |||||||||||||
IMGT | |||||||||||||
EMBL | DAAA02021163 DAAA02021164 DAAA02021165 | ||||||||||||
GenPept | |||||||||||||
RNA Seq Atlas | 282032 | ||||||||||||