Atlastin-1: Difference between revisions
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{{PBB|geneid=51062}} |
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. --> |
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{{GNF_Protein_box |
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| image = |
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| image_source = |
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| PDB = |
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| Name = Spastic paraplegia 3A (autosomal dominant) |
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| HGNCid = 11231 |
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| Symbol = SPG3A |
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| AltSymbols =; GBP3; AD-FSP; ATL1; FSP1; SPG3; atlastin1 |
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| OMIM = 606439 |
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| ECnumber = |
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| Homologene = 9302 |
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| MGIid = 1921241 |
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| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0003924 |text = GTPase activity}} {{GNF_GO|id=GO:0005525 |text = GTP binding}} |
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| Component = |
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| Process = {{GNF_GO|id=GO:0006955 |text = immune response}} |
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| Orthologs = {{GNF_Ortholog_box |
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| Hs_EntrezGene = 51062 |
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| Hs_Ensembl = ENSG00000198513 |
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| Hs_RefseqProtein = NP_056999 |
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| Hs_RefseqmRNA = NM_015915 |
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| Hs_GenLoc_db = |
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| Hs_GenLoc_chr = 14 |
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| Hs_GenLoc_start = 50096593 |
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| Hs_GenLoc_end = 50169532 |
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| Hs_Uniprot = Q8WXF7 |
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| Mm_EntrezGene = 73991 |
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| Mm_Ensembl = ENSMUSG00000021066 |
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| Mm_RefseqmRNA = NM_178628 |
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| Mm_RefseqProtein = NP_848743 |
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| Mm_GenLoc_db = |
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| Mm_GenLoc_chr = 12 |
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| Mm_GenLoc_start = 70811874 |
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| Mm_GenLoc_end = 70882636 |
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| Mm_Uniprot = Q8BH66 |
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}} |
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}} |
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'''Spastic paraplegia 3A (autosomal dominant)''', also known as '''SPG3A''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51062| accessdate = }}</ref> |
'''Spastic paraplegia 3A (autosomal dominant)''', also known as '''SPG3A''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51062| accessdate = }}</ref> |
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Revision as of 10:19, 9 July 2008
Template:PBB Spastic paraplegia 3A (autosomal dominant), also known as SPG3A, is a human gene.[1]