Homo sapiens (human): 27040
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Entry
27040 CDS
T01001
Symbol
LAT, IMD52, LAT1, pp36
Name
(RefSeq) linker for activation of T cells
KO
K07362
linker for activation of T cells family member 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04014
Ras signaling pathway
hsa04015
Rap1 signaling pathway
hsa04064
NF-kappa B signaling pathway
hsa04650
Natural killer cell mediated cytotoxicity
hsa04658
Th1 and Th2 cell differentiation
hsa04659
Th17 cell differentiation
hsa04660
T cell receptor signaling pathway
hsa04664
Fc epsilon RI signaling pathway
hsa04666
Fc gamma R-mediated phagocytosis
hsa05135
Yersinia infection
hsa05235
PD-L1 expression and PD-1 checkpoint pathway in cancer
Network
nt06183
Yersinia
nt06537
TCR/BCR signaling
Element
N01106
TCR-PLCG-ITPR signaling pathway
N01108
Yersinia YopH to TCR-NFAT signaling pathway
Disease
H02526
Disorders of adaptive immunity
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04014 Ras signaling pathway
27040 (LAT)
04015 Rap1 signaling pathway
27040 (LAT)
04064 NF-kappa B signaling pathway
27040 (LAT)
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
27040 (LAT)
04660 T cell receptor signaling pathway
27040 (LAT)
04658 Th1 and Th2 cell differentiation
27040 (LAT)
04659 Th17 cell differentiation
27040 (LAT)
04664 Fc epsilon RI signaling pathway
27040 (LAT)
04666 Fc gamma R-mediated phagocytosis
27040 (LAT)
09160 Human Diseases
09161 Cancer: overview
05235 PD-L1 expression and PD-1 checkpoint pathway in cancer
27040 (LAT)
09171 Infectious disease: bacterial
05135 Yersinia infection
27040 (LAT)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
LAT
Motif
Other DBs
NCBI-GeneID:
27040
NCBI-ProteinID:
NP_055202
OMIM:
602354
HGNC:
18874
Ensembl:
ENSG00000213658
UniProt:
O43561
LinkDB
All DBs
Position
16:28984803..28990784
Genome browser
AA seq
262 aa
AA seq
DB search
MEEAILVPCVLGLLLLPILAMLMALCVHCHRLPGSYDSTSSDSLYPRGIQFKRPHTVAPW
PPAYPPVTSYPPLSQPDLLPIPRSPQPLGGSHRTPSSRRDSDGANSVASYENEGASGIRG
AQAGWGVWGPSWTRLTPVSLPPEPACEDADEDEDDYHNPGYLVVLPDSTPATSTAAPSAP
ALSTPGIRDSAFSMESIDDYVNVPESGESAEASLDGSREYVNVSQELHPGAAKTEPAALS
SQEAEEVEEEGAPDYENLQELN
NT seq
789 nt
NT seq
+upstream
nt +downstream
nt
atggaggaggccatcctggtcccctgcgtgctggggctcctgctgctgcccatcctggcc
atgttgatggcactgtgtgtgcactgccacagactgccaggctcctacgacagcacatcc
tcagatagtttgtatccaaggggcatccagttcaaacggcctcacacggttgccccctgg
ccacctgcctacccacctgtcacctcctacccacccctgagccagccagacctgctcccc
atcccaagatccccgcagccccttgggggctcccaccggacgccatcttcccggcgggat
tctgatggtgccaacagtgtggcgagctacgagaacgagggtgcgtctgggatccgaggt
gcccaggctgggtggggagtctggggtccgtcctggactaggctgacccctgtgtcgtta
cccccagaaccagcctgtgaggatgcggatgaggatgaggacgactatcacaacccaggc
tacctggtggtgcttcctgacagcaccccggccactagcactgctgccccatcagctcct
gcactcagcacccctggcatccgagacagtgccttctccatggagtccattgatgattac
gtgaacgttccggagagcggggagagcgcagaagcgtctctggatggcagccgggagtat
gtgaatgtgtcccaggaactgcatcctggagcggctaagactgagcctgccgccctgagt
tcccaggaggcagaggaagtggaggaagagggggctccagattacgagaatctgcaggag
ctgaactga
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