Homo sapiens (human): 5375 Help Entry 5375              CDS       T01001                                  Symbol PMP2, CMT1G, FABP8, M-FABP, MP2, P2 Name (RefSeq) peripheral myelin protein 2   KO K24977   myelin P2 protein Organism hsa  Homo sapiens (human) Disease H00264   Charcot-Marie-Tooth disease Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99994 Others     5375 (PMP2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Lipocalin Lipocalin_7 SCVP Motif Other DBs NCBI-GeneID:  5375 NCBI-ProteinID:  NP_002668 OMIM:  170715 HGNC:  9117 Ensembl:  ENSG00000147588 UniProt:  P02689 Structure PDBPDBj LinkDB All DBs Position 8:complement(81440326..81447439) Genome browser AA seq 132 aa AA seqDB search MSNKFLGTWKLVSSENFDDYMKALGVGLATRKLGNLAKPTVIISKKGDIITIRTESTFKN TEISFKLGQEFEETTADNRKTKSIVTLQRGSLNQVQRWDGKETTIKRKLVNGKMVAECKM KGVVCTRIYEKV NT seq 399 nt NT seq  +upstreamnt  +downstreamnt atgagcaacaaattcctgggcacctggaaacttgtctctagtgagaactttgacgattac atgaaagctctgggtgtggggttagccaccagaaaactgggaaatttggccaaacccact gtgatcatcagcaagaaaggagatattataactatacgaactgaaagtacctttaaaaat acagaaatctccttcaagctaggccaggaatttgaagaaaccacagctgacaatagaaag accaagagcatcgtaaccctgcagagaggatcactgaatcaagtgcagagatgggatggc aaagagacaaccataaagagaaagctagtgaatgggaaaatggtagcggaatgtaaaatg aagggcgtggtgtgcaccagaatctatgagaaggtctga

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