Homo sapiens (human): 941
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Entry
941 CDS
T01001
Symbol
CD80, B7, B7-1, B7.1, BB1, CD28LG, CD28LG1, LAB7
Name
(RefSeq) CD80 molecule
KO
K05412
CD80 antigen
Organism
hsa
Homo sapiens (human)
Pathway
hsa03267
Virion - Adenovirus
hsa04514
Cell adhesion molecules
hsa04620
Toll-like receptor signaling pathway
hsa04672
Intestinal immune network for IgA production
hsa04940
Type I diabetes mellitus
hsa05320
Autoimmune thyroid disease
hsa05322
Systemic lupus erythematosus
hsa05323
Rheumatoid arthritis
hsa05330
Allograft rejection
hsa05332
Graft-versus-host disease
hsa05416
Viral myocarditis
Network
nt06169
Measles virus (MV)
nt06537
TCR/BCR signaling
Element
N00683
CD80/CD86-CD28-PI3K signaling pathway
N01579
CD80/CD86-CTLA4-PP2A signaling pathway
Drug target
Abatacept:
D03203
<JP/US>
Belatacept:
D03222
<US>
Davoceticept:
D12463
Galiximab:
D04295
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09125 Information processing in viruses
03267 Virion - Adenovirus
941 (CD80)
09150 Organismal Systems
09151 Immune system
04620 Toll-like receptor signaling pathway
941 (CD80)
09160 Human Diseases
09163 Immune disease
05322 Systemic lupus erythematosus
941 (CD80)
05323 Rheumatoid arthritis
941 (CD80)
05320 Autoimmune thyroid disease
941 (CD80)
05330 Allograft rejection
941 (CD80)
05332 Graft-versus-host disease
941 (CD80)
09166 Cardiovascular disease
05416 Viral myocarditis
941 (CD80)
09167 Endocrine and metabolic disease
04940 Type I diabetes mellitus
941 (CD80)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
941 (CD80)
CD molecules [BR:
hsa04090
]
Proteins
941 (CD80)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
C2-set_2
V-set
C2-set_3
Ig_3
ig
I-set
Ig_2
Motif
Other DBs
NCBI-GeneID:
941
NCBI-ProteinID:
NP_005182
OMIM:
112203
HGNC:
1700
Ensembl:
ENSG00000121594
UniProt:
P33681
A0N0P2
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:complement(119524293..119559614)
Genome browser
AA seq
288 aa
AA seq
DB search
MGHTRRQGTSPSKCPYLNFFQLLVLAGLSHFCSGVIHVTKEVKEVATLSCGHNVSVEELA
QTRIYWQKEKKMVLTMMSGDMNIWPEYKNRTIFDITNNLSIVILALRPSDEGTYECVVLK
YEKDAFKREHLAEVTLSVKADFPTPSISDFEIPTSNIRRIICSTSGGFPEPHLSWLENGE
ELNAINTTVSQDPETELYAVSSKLDFNMTTNHSFMCLIKYGHLRVNQTFNWNTTKQEHFP
DNLLPSWAITLISVNGIFVICCLTYCFAPRCRERRRNERLRRESVRPV
NT seq
867 nt
NT seq
+upstream
nt +downstream
nt
atgggccacacacggaggcagggaacatcaccatccaagtgtccatacctcaatttcttt
cagctcttggtgctggctggtctttctcacttctgttcaggtgttatccacgtgaccaag
gaagtgaaagaagtggcaacgctgtcctgtggtcacaatgtttctgttgaagagctggca
caaactcgcatctactggcaaaaggagaagaaaatggtgctgactatgatgtctggggac
atgaatatatggcccgagtacaagaaccggaccatctttgatatcactaataacctctcc
attgtgatcctggctctgcgcccatctgacgagggcacatacgagtgtgttgttctgaag
tatgaaaaagacgctttcaagcgggaacacctggctgaagtgacgttatcagtcaaagct
gacttccctacacctagtatatctgactttgaaattccaacttctaatattagaaggata
atttgctcaacctctggaggttttccagagcctcacctctcctggttggaaaatggagaa
gaattaaatgccatcaacacaacagtttcccaagatcctgaaactgagctctatgctgtt
agcagcaaactggatttcaatatgacaaccaaccacagcttcatgtgtctcatcaagtat
ggacatttaagagtgaatcagaccttcaactggaatacaaccaagcaagagcattttcct
gataacctgctcccatcctgggccattaccttaatctcagtaaatggaatttttgtgata
tgctgcctgacctactgctttgccccaagatgcagagagagaaggaggaatgagagattg
agaagggaaagtgtacgccctgtataa
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