Homo sapiens (human): 497661
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Entry
497661 CDS
T01001
Symbol
C18orf32, GPIBD25
Name
(RefSeq) chromosome 18 open reading frame 32
Organism
hsa
Homo sapiens (human)
Disease
H01489
Inherited glycosylphosphatidylinositol deficiencies
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF4512
Motif
Other DBs
NCBI-GeneID:
497661
NCBI-ProteinID:
NP_001030177
OMIM:
619979
HGNC:
31690
Ensembl:
ENSG00000177576
UniProt:
Q8TCD1
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All DBs
Position
18:complement(49477243..49487234)
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AA seq
76 aa
AA seq
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MVCIPCIVIPVLLWIYKKFLEPYIYPLVSPFVSRIWPKKAIQESNDTNKGKVNFKGADMN
GLPTKGPTEICDKKKD
NT seq
231 nt
NT seq
+upstream
nt +downstream
nt
atggtgtgcattccttgtatcgtcattccagttctgctctggatctacaaaaaattcctg
gagccatatatataccctctggtttcccccttcgttagtcgtatatggcctaagaaagca
atacaagaatccaatgatacaaacaaaggcaaagtaaactttaagggtgcagacatgaat
ggattaccaacaaaaggaccaacagaaatctgtgataaaaagaaagactaa
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