Neogale vison (American mink): 122904716
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Entry
122904716 CDS
T08764
Name
(RefSeq) H-2 class II histocompatibility antigen, E-S beta chain-like
KO
K06752
MHC class II antigen
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04145
Phagosome
nvs04514
Cell adhesion molecules
nvs04612
Antigen processing and presentation
nvs04640
Hematopoietic cell lineage
nvs04658
Th1 and Th2 cell differentiation
nvs04659
Th17 cell differentiation
nvs04672
Intestinal immune network for IgA production
nvs04940
Type I diabetes mellitus
nvs05140
Leishmaniasis
nvs05145
Toxoplasmosis
nvs05150
Staphylococcus aureus infection
nvs05152
Tuberculosis
nvs05164
Influenza A
nvs05166
Human T-cell leukemia virus 1 infection
nvs05168
Herpes simplex virus 1 infection
nvs05169
Epstein-Barr virus infection
nvs05310
Asthma
nvs05320
Autoimmune thyroid disease
nvs05321
Inflammatory bowel disease
nvs05322
Systemic lupus erythematosus
nvs05323
Rheumatoid arthritis
nvs05330
Allograft rejection
nvs05332
Graft-versus-host disease
nvs05416
Viral myocarditis
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecules
122904716
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
122904716
09150 Organismal Systems
09151 Immune system
04640 Hematopoietic cell lineage
122904716
04612 Antigen processing and presentation
122904716
04658 Th1 and Th2 cell differentiation
122904716
04659 Th17 cell differentiation
122904716
04672 Intestinal immune network for IgA production
122904716
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
122904716
05164 Influenza A
122904716
05168 Herpes simplex virus 1 infection
122904716
05169 Epstein-Barr virus infection
122904716
09171 Infectious disease: bacterial
05150 Staphylococcus aureus infection
122904716
05152 Tuberculosis
122904716
09174 Infectious disease: parasitic
05145 Toxoplasmosis
122904716
05140 Leishmaniasis
122904716
09163 Immune disease
05310 Asthma
122904716
05322 Systemic lupus erythematosus
122904716
05323 Rheumatoid arthritis
122904716
05320 Autoimmune thyroid disease
122904716
05321 Inflammatory bowel disease
122904716
05330 Allograft rejection
122904716
05332 Graft-versus-host disease
122904716
09166 Cardiovascular disease
05416 Viral myocarditis
122904716
09167 Endocrine and metabolic disease
04940 Type I diabetes mellitus
122904716
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
nvs04147
]
122904716
Exosome [BR:
nvs04147
]
Exosomal proteins
Exosomal proteins of haemopoietic cells (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
122904716
Exosomal proteins of epithelial cells
122904716
Exosomal proteins of breast milk
122904716
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MHC_II_beta
C1-set
Ig_3
ig
Ig_2
MHC_I
DUF202
Motif
Other DBs
NCBI-GeneID:
122904716
NCBI-ProteinID:
XP_044101799
LinkDB
All DBs
Position
1:119950048..119963414
Genome browser
AA seq
317 aa
AA seq
DB search
MACLWFPRGFWMVALTVILMVLSPPMAWARDTPSRDPVAASPAARRGKTGCVCWWLGAPG
RASEGAAVSVFQEPAGDRIVSVPTAHFLLLTTSECYFTNGTERVRFLDRYFYNGEEYVRF
DSDVGEFRPVTELGRPDAPYWNSQKDFMERARAAVDTYCRHNYGVFESFTVQRRVEPIVT
VYPAKTQPLKHHNLLVCSVNGFYPGHIEVRWFRNGQEEESGVVSTGLICNGDWTFQTLVM
LETVPQSGEVYTCQVEHPSLISPVTVEWRAQTGSAQSKILSGTGGFVLGLLFLVVGLFIY
FRNQKGHSGLQPTGLLN
NT seq
954 nt
NT seq
+upstream
nt +downstream
nt
atggcatgtctgtggttccctagaggcttctggatggtggctctgacagtgatactgatg
gtgctgagccctcccatggcttgggccagggataccccatcccgggacccagtggccgcc
tctcccgccgcccgcagagggaagacgggctgtgtgtgctggtggttgggggcgccgggg
agagccagcgagggagccgccgtcagtgtcttccaggagcccgcgggtgaccggatcgtc
tctgtccccacagcacatttcctgctcctgacgacgtcagaatgctacttcaccaacggc
acggagcgggtgcggttcctggataggtatttctataacggcgaggagtacgtgcgcttc
gacagcgacgtgggggagttccggccggtgaccgagctggggcggccggacgctccgtac
tggaacagccagaaggacttcatggagcgggcgcgggccgccgtggacacgtactgcaga
cacaactacggggtgtttgagagcttcacggtgcagcggcgagtggagcctatagtgact
gtgtatcctgcgaagacccagcccctgaagcaccacaacctcctggtctgctctgtgaat
ggtttctatccaggccacattgaagtcaggtggttccggaatggccaggaagaggagtct
ggggttgtgtccacaggcctgatctgtaatggagactggaccttccagaccctagtgatg
ctggagacagttcctcagagtggagaggtctatacctgccaagtggagcaccccagtttg
ataagccctgtcaccgtggaatggagggcacagactgggtctgcacagagcaagattctg
agtggaactggaggctttgttctgggtctgctcttcctcgtggtggggctgttcatctac
ttcaggaatcagaagggacactctggacttcagccaacaggtctcctgaactga
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