Homo sapiens (human): 83636 Help Entry 83636             CDS       T01001                                  Symbol C19orf12, MPAN, NBIA3, NBIA4, SPG43 Name (RefSeq) protein C19orf12 isoform 2   KO K23168   protein MPAN Organism hsa  Homo sapiens (human) Disease H00266   Hereditary spastic paraplegia H00833   Neurodegeneration with brain iron accumulation Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:hsa03029]     83636 (C19orf12) Mitochondrial biogenesis [BR:hsa03029]  Mitochondrial quality control factors   Mitophagy factors    Other mitophagy factors     83636 (C19orf12) SSDB OrthologParalogGFIT Motif Pfam:  C19orf12 Gly-zipper_YMGG Y2009_N DUF5862 Motif Other DBs NCBI-GeneID:  83636 NCBI-ProteinID:  NP_001026896 OMIM:  614297 HGNC:  25443 UniProt:  Q9NSK7 LinkDB All DBs Position 19:complement(29698886..29715789) Genome browser AA seq 141 aa AA seqDB search MTIMVEDIMKLLCSLSGERKMKAAVKHSGKGALVTGAMAFVGGLVGGPPGLAVGGAVGGL LGAWMTSGQFKPVPQILMELPPAEQQRLFNEAAAIIRHLEWTDAVQLTALVMGSEALQQQ LLAMLVNYVTKELRAEIQYDD NT seq 426 nt NT seq  +upstreamnt  +downstreamnt atgactatcatggtggaggacatcatgaagctgctgtgctccctttctggggagaggaag atgaaggcggctgtcaagcactctgggaagggtgccctggtcacaggggccatggccttc gtcgggggtttggtgggcggcccaccgggactcgccgttgggggggctgtcggggggctg ttaggtgcctggatgacaagtggacagtttaagccggttcctcagatcctaatggagctg ccccctgccgagcaacagaggctctttaacgaagccgcagccatcatcaggcacctggag tggacggacgccgtgcagctgaccgcgctggtcatgggcagcgaggccctgcagcagcag ctgctggccatgctggtgaactacgtcaccaaggagctgcgggccgagatccagtatgat gactag

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