Bos taurus Gene: SEMA4A | |||||||||||||||||
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Summary | |||||||||||||||||
InnateDB Gene | IDBG-631665.3 | ||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||
Gene Symbol | SEMA4A | ||||||||||||||||
Gene Name | semaphorin-4A precursor | ||||||||||||||||
Synonyms | |||||||||||||||||
Species | Bos taurus | ||||||||||||||||
Ensembl Gene | ENSBTAG00000012228 | ||||||||||||||||
Encoded Proteins |
semaphorin-4A precursor
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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 ENSG00000196189:
This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010] |
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Gene Information | |||||||||||||||||
Type | Protein coding | ||||||||||||||||
Genomic Location | Chromosome 3:14659269-14679216 | ||||||||||||||||
Strand | Reverse 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 5 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 | |||||||||||||||||
REACTOME |
Other semaphorin interactions pathway
Developmental Biology pathway
Semaphorin interactions pathway
Axon guidance pathway
Axon guidance pathway
Developmental Biology pathway
Semaphorin interactions pathway
Other semaphorin interactions pathway
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KEGG |
Axon guidance pathway
Axon guidance pathway
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INOH | |||||||||||||||||
PID NCI |
Plexin-D1 Signaling
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Cross-References | |||||||||||||||||
SwissProt | |||||||||||||||||
TrEMBL | F1MY79 | ||||||||||||||||
UniProt Splice Variant | |||||||||||||||||
Entrez Gene | 510239 | ||||||||||||||||
UniGene | Bt.3339 | ||||||||||||||||
RefSeq | NM_001075440 XM_005203689 XM_005203690 XM_005203691 XM_005203692 | ||||||||||||||||
HUGO | HGNC:10729 | ||||||||||||||||
OMIM | |||||||||||||||||
CCDS | |||||||||||||||||
HPRD | |||||||||||||||||
IMGT | |||||||||||||||||
EMBL | DAAA02007141 DAAA02007142 DAAA02007143 | ||||||||||||||||
GenPept | |||||||||||||||||
RNA Seq Atlas | 510239 | ||||||||||||||||