Homo sapiens (human): 83452 Help Entry 83452             CDS       T01001                                  Symbol RAB33B, SMC2 Name (RefSeq) ras-related protein Rab-33B   KO K07920   Ras-related protein Rab-33B Organism hsa  Homo sapiens (human) Pathway hsa04140   Autophagy - animal Disease H02497   Smith-McCort dysplasia Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04140 Autophagy - animal     83452 (RAB33B)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04131 Membrane trafficking [BR:hsa04131]     83452 (RAB33B)   09183 Protein families: signaling and cellular processes    04147 Exosome [BR:hsa04147]     83452 (RAB33B)    04031 GTP-binding proteins [BR:hsa04031]     83452 (RAB33B) Membrane trafficking [BR:hsa04131]  Endoplasmic reticulum (ER) - Golgi transport   Retrieval pathways    Rab GTPases     83452 (RAB33B)  Others   Specific organelles associated proteins    Auto phagosome     83452 (RAB33B) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of colorectal cancer cells    83452 (RAB33B) GTP-binding proteins [BR:hsa04031]  Small (monomeric) G-proteins   Rab Family    Rab33     83452 (RAB33B) SSDB OrthologParalogGFIT Motif Pfam:  Ras Roc Arf GTP_EFTU MMR_HSR1 Gtr1_RagA G-alpha SRPRB ATP_bind_1 TniB PduV-EutP Motif Other DBs NCBI-GeneID:  83452 NCBI-ProteinID:  NP_112586 OMIM:  605950 HGNC:  16075 Ensembl:  ENSP00000306496.5 UniProt:  Q9H082 Structure PDBPDBj LinkDB All DBs Position 4:139438376..139476609 Genome browser AA seq 229 aa AA seqDB search MAEEMESSLEASFSSSGAVSGASGFLPPARSRIFKIIVIGDSNVGKTCLTYRFCAGRFPD RTEATIGVDFRERAVEIDGERIKIQLWDTAGQERFRKSMVQHYYRNVHAVVFVYDMTNMA SFHSLPSWIEECKQHLLANDIPRILVGNKCDLRSAIQVPTDLAQKFADTHSMPLFETSAK NPNDNDHVEAIFMTLAHKLKSHKPLMLSQPPDNGIILKPEPKPAMTCWC NT seq 690 nt NT seq  +upstreamnt  +downstreamnt atggctgaggagatggagtcgtcgctcgaggcaagcttttcgtccagcggggcagtgtca ggggcctcagggtttttgcctcctgcccgctcccgcatcttcaagataatcgtgatcggc gactccaatgtgggcaagacatgcctgacctaccgcttctgcgctggccgcttccccgac cgcaccgaggccacgataggggtggatttccgagaacgagcggtggagattgatggggag cgcatcaagatccagctatgggacacagcaggacaagaacgattcagaaagagcatggtt cagcactactacagaaatgtacatgctgttgtcttcgtgtatgatatgaccaacatggct agttttcatagcctaccatcttggatagaagaatgcaaacaacatttgctagccaatgat ataccacggattcttgttggaaataaatgtgacttgagaagtgccatacaggtacccaca gacttggcacaaaaatttgctgacacacacagtatgcctttgtttgaaacgtctgctaaa aaccccaatgataatgaccatgtggaagctatatttatgaccttggctcataagcttaag agccacaaaccattaatgcttagtcagccccctgataatggaattatcctgaagcctgaa ccaaagcctgcaatgacgtgctggtgctaa

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