KEGG   Ursus maritimus (polar bear): 103665509
Entry
103665509         CDS       T03271                                 
Name
(RefSeq) HLA class II histocompatibility antigen, DM beta chain isoform X1
  KO
K06752  MHC class II antigen
Organism
umr  Ursus maritimus (polar bear)
Pathway
umr04145  Phagosome
umr04514  Cell adhesion molecules
umr04612  Antigen processing and presentation
umr04640  Hematopoietic cell lineage
umr04658  Th1 and Th2 cell differentiation
umr04659  Th17 cell differentiation
umr04672  Intestinal immune network for IgA production
umr04940  Type I diabetes mellitus
umr05140  Leishmaniasis
umr05145  Toxoplasmosis
umr05150  Staphylococcus aureus infection
umr05152  Tuberculosis
umr05164  Influenza A
umr05166  Human T-cell leukemia virus 1 infection
umr05168  Herpes simplex virus 1 infection
umr05169  Epstein-Barr virus infection
umr05310  Asthma
umr05320  Autoimmune thyroid disease
umr05321  Inflammatory bowel disease
umr05322  Systemic lupus erythematosus
umr05323  Rheumatoid arthritis
umr05330  Allograft rejection
umr05332  Graft-versus-host disease
umr05416  Viral myocarditis
Brite
KEGG Orthology (KO) [BR:umr00001]
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    103665509
 09140 Cellular Processes
  09141 Transport and catabolism
   04145 Phagosome
    103665509
 09150 Organismal Systems
  09151 Immune system
   04640 Hematopoietic cell lineage
    103665509
   04612 Antigen processing and presentation
    103665509
   04658 Th1 and Th2 cell differentiation
    103665509
   04659 Th17 cell differentiation
    103665509
   04672 Intestinal immune network for IgA production
    103665509
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    103665509
   05164 Influenza A
    103665509
   05168 Herpes simplex virus 1 infection
    103665509
   05169 Epstein-Barr virus infection
    103665509
  09171 Infectious disease: bacterial
   05150 Staphylococcus aureus infection
    103665509
   05152 Tuberculosis
    103665509
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    103665509
   05140 Leishmaniasis
    103665509
  09163 Immune disease
   05310 Asthma
    103665509
   05322 Systemic lupus erythematosus
    103665509
   05323 Rheumatoid arthritis
    103665509
   05320 Autoimmune thyroid disease
    103665509
   05321 Inflammatory bowel disease
    103665509
   05330 Allograft rejection
    103665509
   05332 Graft-versus-host disease
    103665509
  09166 Cardiovascular disease
   05416 Viral myocarditis
    103665509
  09167 Endocrine and metabolic disease
   04940 Type I diabetes mellitus
    103665509
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:umr04147]
    103665509
Exosome [BR:umr04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   103665509
  Exosomal proteins of epithelial cells
   103665509
  Exosomal proteins of breast milk
   103665509
SSDB
Motif
Pfam: C1-set MHC_II_beta Ig_2 Ig_3 I-set C2-set_2 ig C2-set_3
Other DBs
NCBI-GeneID: 103665509
NCBI-ProteinID: XP_008691675
UniProt: A0A384CA42 A0A452U8Y9
LinkDB
Position
Unknown
AA seq 263 aa
MTTLLPLLLGLSLGSTTAGGFIAHVESACLLDDDGTPKDFAYCVSFNKDLLTCWDSVEGK
MAPCEFGALTFLAKYLSDYLNQQEPLLQRLSNGLQDCAARTQSFWGSLTRRTRPPTVQVA
KTTPFNTKEHVMLACYVWGFYPADVTISWRKNGQPVPPHSSAPKMAQPNGDWTYQTVSYL
ATTPSYGDTYTCVVEHIGAPEPVCEDWTAGLSPMQTVKVSLSAVTLGLGFIIFFLGLLSW
RRAGPSGYILLPGDSYPEGQHVN
NT seq 792 nt   +upstreamnt  +downstreamnt
atgaccacactcctgcccttgctgctgggcctcagcctgggctccaccacagcaggtggc
tttatagcccatgtggaaagcgcctgtctgttggatgatgatgggactccaaaggatttc
gcatattgtgtctccttcaacaaggatttgttgacctgctgggattcggtggagggcaaa
atggccccttgtgaatttggggcactgactttcttggccaagtacctctcagattacctc
aaccaacaggaacccctgctccagcgcttgtctaatgggctccaggactgtgctgcacgt
acccagtccttctggggatcactgacccgcaggacaaggccaccgactgtgcaagtagcc
aaaaccactccttttaacacgaaggagcatgtgatgctggcctgctacgtgtggggcttc
tatccagctgatgtgaccatctcgtggaggaagaacgggcagcctgtccctcctcacagt
agcgcccctaagatggcccagcccaatggagactggacataccagactgtctcctattta
gctaccaccccctcttacggggacacctacacctgtgtggtggagcacatcggggctcct
gagcccgtctgcgaggactggacagctgggctgtccccgatgcagacagtgaaggtttct
ctgtctgcagtgactctgggcctgggcttcatcattttctttcttggtttgctcagctgg
cggagagctggcccctctggctacattttgcttcctggggacagttatcctgaaggtcaa
cacgtcaattag

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