Homo sapiens (human): 22808 Help Entry 22808             CDS       T01001                                  Symbol MRAS, M-RAs, NS11, R-RAS3, RRAS3 Name (RefSeq) muscle RAS oncogene homolog   KO K07831   Ras-related protein M-Ras Organism hsa  Homo sapiens (human) Pathway hsa04010   MAPK signaling pathway hsa04014   Ras signaling pathway hsa04015   Rap1 signaling pathway hsa04072   Phospholipase D signaling pathway hsa04137   Mitophagy - animal hsa04140   Autophagy - animal hsa04218   Cellular senescence hsa04371   Apelin signaling pathway hsa04625   C-type lectin receptor signaling pathway hsa04810   Regulation of actin cytoskeleton hsa05205   Proteoglycans in cancer Network nt06526  MAPK signaling   Element N01598   Regulation of GF-RTK-RAS-ERK signaling, MRAS-SHOC2-PP1 holophosphatase Disease H01738   Noonan syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04014 Ras signaling pathway     22808 (MRAS)    04015 Rap1 signaling pathway     22808 (MRAS)    04072 Phospholipase D signaling pathway     22808 (MRAS)  09140 Cellular Processes   09141 Transport and catabolism    04140 Autophagy - animal     22808 (MRAS)    04137 Mitophagy - animal     22808 (MRAS)  09160 Human Diseases   09161 Cancer: overview    05205 Proteoglycans in cancer     22808 (MRAS)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04031 GTP-binding proteins [BR:hsa04031]     22808 (MRAS) GTP-binding proteins [BR:hsa04031]  Small (monomeric) G-proteins   Ras Family    Ras [OT]     22808 (MRAS) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Ras Roc GTP_EFTU Arf RsgA_GTPase MMR_HSR1 ATP_bind_1 AAA_16 MMR_HSR1_Xtn Motif Other DBs NCBI-GeneID:  22808 NCBI-ProteinID:  NP_001078518 OMIM:  608435 HGNC:  7227 Ensembl:  ENSG00000158186 UniProt:  O14807 Q6FGP0 Q8WVM9 Structure PDBPDBj LinkDB All DBs Position 3:138347648..138405535 Genome browser AA seq 208 aa AA seqDB search MATSAVPSDNLPTYKLVVVGDGGVGKSALTIQFFQKIFVPDYDPTIEDSYLKHTEIDNQW AILDVLDTAGQEEFSAMREQYMRTGDGFLIVYSVTDKASFEHVDRFHQLILRVKDRESFP MILVANKVDLMHLRKITREQGKEMATKHNIPYIETSAKDPPLNVDKAFHDLVRVIRQQIP EKSQKKKKKTKWRGDRATGTHKLQCVIL NT seq 627 nt NT seq  +upstreamnt  +downstreamnt atggcaaccagcgccgtccccagtgacaacctccccacatacaagctggtggtggtgggg gatgggggtgtgggcaaaagtgccctcaccatccagtttttccagaagatctttgtgcct gactatgaccccaccattgaagactcctacctgaaacatacggagattgacaatcaatgg gccatcttggacgttctggacacagctgggcaggaggaattcagcgccatgcgggagcaa tacatgcgcacgggggatggcttcctcatcgtctactccgtcactgacaaggccagcttt gagcacgtggaccgcttccaccagcttatcctgcgcgtcaaagacagggagtcattcccg atgatcctcgtggccaacaaggtcgatttgatgcacttgaggaagatcaccagggagcaa ggaaaagaaatggcgaccaaacacaatattccgtacatagaaaccagtgccaaggaccca cctctcaatgtcgacaaagccttccatgacctcgttagagtaattaggcaacagattccg gaaaaaagccagaagaagaagaagaaaaccaaatggcggggagaccgggccacaggcacc cacaaactgcaatgtgtgatcttgtga

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