KEGG   Prionailurus bengalensis (leopard cat): 122489382
Entry
122489382         CDS       T07574                                 
Name
(RefSeq) HLA class II histocompatibility antigen, DM alpha chain
  KO
K06752  MHC class II antigen
Organism
pbg  Prionailurus bengalensis (leopard cat)
Pathway
pbg04145  Phagosome
pbg04514  Cell adhesion molecules
pbg04612  Antigen processing and presentation
pbg04640  Hematopoietic cell lineage
pbg04658  Th1 and Th2 cell differentiation
pbg04659  Th17 cell differentiation
pbg04672  Intestinal immune network for IgA production
pbg04940  Type I diabetes mellitus
pbg05140  Leishmaniasis
pbg05145  Toxoplasmosis
pbg05150  Staphylococcus aureus infection
pbg05152  Tuberculosis
pbg05164  Influenza A
pbg05166  Human T-cell leukemia virus 1 infection
pbg05168  Herpes simplex virus 1 infection
pbg05169  Epstein-Barr virus infection
pbg05310  Asthma
pbg05320  Autoimmune thyroid disease
pbg05321  Inflammatory bowel disease
pbg05322  Systemic lupus erythematosus
pbg05323  Rheumatoid arthritis
pbg05330  Allograft rejection
pbg05332  Graft-versus-host disease
pbg05416  Viral myocarditis
Brite
KEGG Orthology (KO) [BR:pbg00001]
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    122489382
 09140 Cellular Processes
  09141 Transport and catabolism
   04145 Phagosome
    122489382
 09150 Organismal Systems
  09151 Immune system
   04640 Hematopoietic cell lineage
    122489382
   04612 Antigen processing and presentation
    122489382
   04658 Th1 and Th2 cell differentiation
    122489382
   04659 Th17 cell differentiation
    122489382
   04672 Intestinal immune network for IgA production
    122489382
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122489382
   05164 Influenza A
    122489382
   05168 Herpes simplex virus 1 infection
    122489382
   05169 Epstein-Barr virus infection
    122489382
  09171 Infectious disease: bacterial
   05150 Staphylococcus aureus infection
    122489382
   05152 Tuberculosis
    122489382
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    122489382
   05140 Leishmaniasis
    122489382
  09163 Immune disease
   05310 Asthma
    122489382
   05322 Systemic lupus erythematosus
    122489382
   05323 Rheumatoid arthritis
    122489382
   05320 Autoimmune thyroid disease
    122489382
   05321 Inflammatory bowel disease
    122489382
   05330 Allograft rejection
    122489382
   05332 Graft-versus-host disease
    122489382
  09166 Cardiovascular disease
   05416 Viral myocarditis
    122489382
  09167 Endocrine and metabolic disease
   04940 Type I diabetes mellitus
    122489382
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:pbg04147]
    122489382
Exosome [BR:pbg04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   122489382
  Exosomal proteins of epithelial cells
   122489382
  Exosomal proteins of breast milk
   122489382
SSDB
Motif
Pfam: MHC_II_alpha C1-set
Other DBs
NCBI-GeneID: 122489382
NCBI-ProteinID: XP_043447048
LinkDB
Position
B2:complement(31474595..31478427)
AA seq 261 aa
MDHEQRQGAALLRFLHLLWLLPHSWTSPEAPTPVWQDELQNHTFLHTMYCQDWSPNIGLS
ETYDGDQLFSFDFSQNTRVPRLPEFADWAQKLGDTSAIFFDEAFCQAMIREIGPKLEGKI
PVSRGLPVVEVFTLKPLEFGKPNTLVCFVSNLFPPTLTVNWQHHLDPVEGVRPTFVSAVD
GLSFQAFSYLNFTPVPSDLYSCMVTHEIDNYSAIAFWVPHNALPSDLLENVLCGVAFGLG
MLGIIVGLVLIIYFRKPCSGD
NT seq 786 nt   +upstreamnt  +downstreamnt
atggatcatgagcagaggcagggagctgcactgctaaggtttttacacctcctgtggctg
ctgccccactcctggacctcccctgaagctcctaccccagtgtggcaggatgaactgcaa
aaccacacgttcctgcatacgatgtactgccaggactggagtcccaacattggactctct
gaaacctatgatggagaccagcttttctccttcgacttttcccagaatacccgagtgcct
cgcctgcctgaatttgctgactgggctcagaagcttggagatacttctgccattttcttt
gacgaagcattctgccaggctatgatccgggaaatagggccaaaacttgaagggaaaatc
cctgtgtctagagggttacctgttgttgaggtgttcacgctgaagcccctggagtttgga
aagcccaacacgctggtctgttttgtcagtaatctcttcccacccacgttgacggtgaac
tggcagcatcatttggaccctgtggaaggagtcaggcccacttttgtgtcagctgtggat
ggactcagcttccaggccttttcttacttaaacttcacaccagtaccctctgacctttac
tcctgcatggtaactcatgagattgacaactacagcgcaattgccttttgggtgccccat
aatgcactgccctctgatcttctggagaatgtgctgtgtggtgtggcctttggcctgggt
atgctgggcatcattgttggcttagtcctcatcatctacttccgaaagccttgctcaggt
gattga

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