Homo sapiens (human): 51569 Help Entry 51569             CDS       T01001                                  Symbol UFM1, BM-002, C13orf20, HLD14 Name (RefSeq) ubiquitin fold modifier 1   KO K12162   ubiquitin-fold modifier 1 Organism hsa  Homo sapiens (human) Disease H00679   Hypomyelinating leukodystrophy Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04121 Ubiquitin system [BR:hsa04121]     51569 (UFM1) Ubiquitin system [BR:hsa04121]  Ubiquitins and ubiquitin-like proteins   Ubiquitin-like proteins (UBLs)    51569 (UFM1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Ufm1 Motif Other DBs NCBI-GeneID:  51569 NCBI-ProteinID:  NP_057701 OMIM:  610553 HGNC:  20597 Ensembl:  ENSG00000120686 UniProt:  P61960 Structure PDBPDBj LinkDB All DBs Position 13:38349851..38363619 Genome browser AA seq 85 aa AA seqDB search MSKVSFKITLTSDPRLPYKVLSVPESTPFTAVLKFAAEEFKVPAATSAIITNDGIGINPA QTAGNVFLKHGSELRIIPRDRVGSC NT seq 258 nt NT seq  +upstreamnt  +downstreamnt atgtcgaaggtttcctttaagatcacgctgacgtcggacccacggctgccgtacaaagta ctcagtgttcctgaaagtacacctttcacagcagtcttaaagtttgcagcagaagaattt aaagttcctgctgcaacaagtgcaattattaccaatgatggaataggaataaatcctgca cagactgctggaaatgtttttctaaaacatggttcagaactgcggattattcctagagat cgtgttggaagttgttaa

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