(Translated by https://www.hiragana.jp/)
KEGG T03372: 103747703
KEGG   Nannospalax galili (Upper Galilee mountains blind mole rat): 103747703
Entry
103747703         CDS       T03372                                 
Name
(RefSeq) HLA class II histocompatibility antigen, DP alpha 1 chain-like
  KO
K06752  MHC class II antigen
Organism
ngi  Nannospalax galili (Upper Galilee mountains blind mole rat)
Pathway
ngi04145  Phagosome
ngi04514  Cell adhesion molecules
ngi04612  Antigen processing and presentation
ngi04640  Hematopoietic cell lineage
ngi04658  Th1 and Th2 cell differentiation
ngi04659  Th17 cell differentiation
ngi04672  Intestinal immune network for IgA production
ngi04940  Type I diabetes mellitus
ngi05140  Leishmaniasis
ngi05145  Toxoplasmosis
ngi05150  Staphylococcus aureus infection
ngi05152  Tuberculosis
ngi05164  Influenza A
ngi05166  Human T-cell leukemia virus 1 infection
ngi05168  Herpes simplex virus 1 infection
ngi05169  Epstein-Barr virus infection
ngi05310  Asthma
ngi05320  Autoimmune thyroid disease
ngi05321  Inflammatory bowel disease
ngi05322  Systemic lupus erythematosus
ngi05323  Rheumatoid arthritis
ngi05330  Allograft rejection
ngi05332  Graft-versus-host disease
ngi05416  Viral myocarditis
Brite
KEGG Orthology (KO) [BR:ngi00001]
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    103747703
 09140 Cellular Processes
  09141 Transport and catabolism
   04145 Phagosome
    103747703
 09150 Organismal Systems
  09151 Immune system
   04640 Hematopoietic cell lineage
    103747703
   04612 Antigen processing and presentation
    103747703
   04658 Th1 and Th2 cell differentiation
    103747703
   04659 Th17 cell differentiation
    103747703
   04672 Intestinal immune network for IgA production
    103747703
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    103747703
   05164 Influenza A
    103747703
   05168 Herpes simplex virus 1 infection
    103747703
   05169 Epstein-Barr virus infection
    103747703
  09171 Infectious disease: bacterial
   05150 Staphylococcus aureus infection
    103747703
   05152 Tuberculosis
    103747703
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    103747703
   05140 Leishmaniasis
    103747703
  09163 Immune disease
   05310 Asthma
    103747703
   05322 Systemic lupus erythematosus
    103747703
   05323 Rheumatoid arthritis
    103747703
   05320 Autoimmune thyroid disease
    103747703
   05321 Inflammatory bowel disease
    103747703
   05330 Allograft rejection
    103747703
   05332 Graft-versus-host disease
    103747703
  09166 Cardiovascular disease
   05416 Viral myocarditis
    103747703
  09167 Endocrine and metabolic disease
   04940 Type I diabetes mellitus
    103747703
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:ngi04147]
    103747703
Exosome [BR:ngi04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   103747703
  Exosomal proteins of epithelial cells
   103747703
  Exosomal proteins of breast milk
   103747703
SSDB
Motif
Pfam: MHC_II_alpha C1-set Ig_3 Ig_2
Other DBs
NCBI-GeneID: 103747703
NCBI-ProteinID: XP_008848487
LinkDB
Position
Un
AA seq 260 aa
MCSEDRMFQTKAVVPRALFLALLLSLPGAEAIKADHVAMFDIFTQTQKPSGECLYEFDGD
EIFYVDQDKRETIWHLQQFGKDFSFDAQGGLANMAIAKTNLETLIQMSNHTQGRSEPPEV
TVFPKSPVELGQPNVLICHIDKFFPPVLNVTWLRNGQPVTEGASETIFLPSTEFRFHKFH
YLTFIPTAEDFYDCRVEHWGLDQPSVSHWDMQEPIQVTETTETVVCALGLVVGLVGIIVG
SMFIIRALHSSRDPRAQGPL
NT seq 783 nt   +upstreamnt  +downstreamnt
atgtgctctgaagacagaatgttccagaccaaggctgtggtcccgagagccctcttcctg
gctcttctgctgagtctcccaggagctgaggccatcaaggcggaccatgtagcaatgttt
gacatatttacacagacacaaaagccatctggagagtgcttgtatgagtttgatggagac
gagatattctacgtggatcaggacaagagggagaccatctggcatcttcagcagtttggc
aaagactttagctttgatgctcagggtggactggcaaatatggccatagcaaagacaaac
ttggaaaccttgatccagatgagcaaccacacccaggggagaagtgagcctcctgaagtg
actgtgtttcccaagagccctgtggagctgggccagcccaacgtcctcatctgtcacatt
gacaagttcttccccccggtgctcaatgtcacgtggctaagaaatggacagcccgtcact
gaaggagcttctgagaccatctttctgcccagcacagaattcagattccacaagttccat
tacctgaccttcattcccacggccgaggacttctatgactgccgggtagagcactggggc
ctggaccagccgagcgtcagtcactgggacatgcaggagccaatccaggtgacagagacg
acggagactgtggtctgtgcgctgggcctggtggtgggcctggtgggcatcattgtgggc
tccatgttcatcataagggctctgcactctagccgtgacccccgggcccagggacctctg
tga

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