KEGG   Homo sapiens (human): 1604
Entry
1604              CDS       T01001                                 
Symbol
CD55, CHAPLE, CR, CROM, DAF, TC
Name
(RefSeq) CD55 molecule (Cromer blood group)
  KO
K04006  decay accelerating factor
Organism
hsa  Homo sapiens (human)
Pathway
hsa04610  Complement and coagulation cascades
hsa04640  Hematopoietic cell lineage
hsa05416  Viral myocarditis
Network
nt06513  Complement cascade
  Element
N01496  Alternative pathway of complement cascade, C3b breakdown
Disease
H00106  Complement regulatory protein defects
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09151 Immune system
   04640 Hematopoietic cell lineage
    1604 (CD55)
   04610 Complement and coagulation cascades
    1604 (CD55)
 09160 Human Diseases
  09166 Cardiovascular disease
   05416 Viral myocarditis
    1604 (CD55)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    1604 (CD55)
   04090 CD molecules [BR:hsa04090]
    1604 (CD55)
   00537 Glycosylphosphatidylinositol (GPI)-anchored proteins [BR:hsa00537]
    1604 (CD55)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   1604 (CD55)
  Exosomal proteins of other body fluids (saliva and urine)
   1604 (CD55)
  Exosomal proteins of colorectal cancer cells
   1604 (CD55)
CD molecules [BR:hsa04090]
 Proteins
  1604 (CD55)
Glycosylphosphatidylinositol (GPI)-anchored proteins [BR:hsa00537]
 Antigens
  1604 (CD55)
SSDB
Motif
Pfam: Sushi
Other DBs
NCBI-GeneID: 1604
NCBI-ProteinID: NP_000565
OMIM: 125240
HGNC: 2665
Ensembl: ENSG00000196352
UniProt: P08174
Structure
Position
1:207321678..207360966
AA seq 381 aa
MTVARPSVPAALPLLGELPRLLLLVLLCLPAVWGDCGLPPDVPNAQPALEGRTSFPEDTV
ITYKCEESFVKIPGEKDSVICLKGSQWSDIEEFCNRSCEVPTRLNSASLKQPYITQNYFP
VGTVVEYECRPGYRREPSLSPKLTCLQNLKWSTAVEFCKKKSCPNPGEIRNGQIDVPGGI
LFGATISFSCNTGYKLFGSTSSFCLISGSSVQWSDPLPECREIYCPAPPQIDNGIIQGER
DHYGYRQSVTYACNKGFTMIGEHSIYCTVNNDEGEWSGPPPECRGKSLTSKVPPTVQKPT
TVNVPTTEVSPTSQKTTTKTTTPNAQATRSTPVSRTTKHFHETTPNKGSGTTSGTTRLLS
GHTCFTLTGLLGTLVTMGLLT
NT seq 1146 nt   +upstreamnt  +downstreamnt
atgaccgtcgcgcggccgagcgtgcccgcggcgctgcccctcctcggggagctgccccgg
ctgctgctgctggtgctgttgtgcctgccggccgtgtggggtgactgtggccttccccca
gatgtacctaatgcccagccagctttggaaggccgtacaagttttcccgaggatactgta
ataacgtacaaatgtgaagaaagctttgtgaaaattcctggcgagaaggactcagtgatc
tgccttaagggcagtcaatggtcagatattgaagagttctgcaatcgtagctgcgaggtg
ccaacaaggctaaattctgcatccctcaaacagccttatatcactcagaattattttcca
gtcggtactgttgtggaatatgagtgccgtccaggttacagaagagaaccttctctatca
ccaaaactaacttgccttcagaatttaaaatggtccacagcagtcgaattttgtaaaaag
aaatcatgccctaatccgggagaaatacgaaatggtcagattgatgtaccaggtggcata
ttatttggtgcaaccatctccttctcatgtaacacagggtacaaattatttggctcgact
tctagtttttgtcttatttcaggcagctctgtccagtggagtgacccgttgccagagtgc
agagaaatttattgtccagcaccaccacaaattgacaatggaataattcaaggggaacgt
gaccattatggatatagacagtctgtaacgtatgcatgtaataaaggattcaccatgatt
ggagagcactctatttattgtactgtgaataatgatgaaggagagtggagtggcccacca
cctgaatgcagaggaaaatctctaacttccaaggtcccaccaacagttcagaaacctacc
acagtaaatgttccaactacagaagtctcaccaacttctcagaaaaccaccacaaaaacc
accacaccaaatgctcaagcaacacggagtacacctgtttccaggacaaccaagcatttt
catgaaacaaccccaaataaaggaagtggaaccacttcaggtactacccgtcttctatct
gggcacacgtgtttcacgttgacaggtttgcttgggacgctagtaaccatgggcttgctg
acttag

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