KEGG   Homo sapiens (human): 51569
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)
SSDB
Motif
Pfam: Ufm1
Other DBs
NCBI-GeneID: 51569
NCBI-ProteinID: NP_057701
OMIM: 610553
HGNC: 20597
Ensembl: ENSG00000120686
UniProt: P61960
Structure
Position
13:38349851..38363619
AA seq 85 aa
MSKVSFKITLTSDPRLPYKVLSVPESTPFTAVLKFAAEEFKVPAATSAIITNDGIGINPA
QTAGNVFLKHGSELRIIPRDRVGSC
NT seq 258 nt   +upstreamnt  +downstreamnt
atgtcgaaggtttcctttaagatcacgctgacgtcggacccacggctgccgtacaaagta
ctcagtgttcctgaaagtacacctttcacagcagtcttaaagtttgcagcagaagaattt
aaagttcctgctgcaacaagtgcaattattaccaatgatggaataggaataaatcctgca
cagactgctggaaatgtttttctaaaacatggttcagaactgcggattattcctagagat
cgtgttggaagttgttaa

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