KEGG   Homo sapiens (human): 497661
Entry
497661            CDS       T01001                                 
Symbol
C18orf32, GPIBD25
Name
(RefSeq) chromosome 18 open reading frame 32
  KO
K28352  UPF0729 protein C18orf32
Organism
hsa  Homo sapiens (human)
Disease
H01489  Inherited glycosylphosphatidylinositol deficiencies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    497661 (C18orf32)
Membrane trafficking [BR:hsa04131]
 Others
  Specific organelles associated proteins
   Lipid droplets
    497661 (C18orf32)
SSDB
Motif
Pfam: DUF4512
Other DBs
NCBI-GeneID: 497661
NCBI-ProteinID: NP_001030177
OMIM: 619979
HGNC: 31690
Ensembl: ENSG00000177576
UniProt: Q8TCD1
LinkDB
Position
18:complement(49477243..49487234)
AA seq 76 aa
MVCIPCIVIPVLLWIYKKFLEPYIYPLVSPFVSRIWPKKAIQESNDTNKGKVNFKGADMN
GLPTKGPTEICDKKKD
NT seq 231 nt   +upstreamnt  +downstreamnt
atggtgtgcattccttgtatcgtcattccagttctgctctggatctacaaaaaattcctg
gagccatatatataccctctggtttcccccttcgttagtcgtatatggcctaagaaagca
atacaagaatccaatgatacaaacaaaggcaaagtaaactttaagggtgcagacatgaat
ggattaccaacaaaaggaccaacagaaatctgtgataaaaagaaagactaa

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