Homo sapiens (human): 7462
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Entry
7462 CDS
T01001
Symbol
LAT2, HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5
Name
(RefSeq) linker for activation of T cells family member 2
KO
K26356
linker for activation of T-cells family member 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04650
Natural killer cell mediated cytotoxicity
Disease
H01439
Williams-Beuren syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
7462 (LAT2)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
LAT2
PycTM
Motif
Other DBs
NCBI-GeneID:
7462
NCBI-ProteinID:
NP_054865
OMIM:
605719
HGNC:
12749
Ensembl:
ENSG00000086730
UniProt:
Q9GZY6
Structure
PDB
PDBj
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All DBs
Position
7:74210006..74229834
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AA seq
243 aa
AA seq
DB search
MSSGTELLWPGAALLVLLGVAASLCVRCSRPGAKRSEKIYQQRSLREDQQSFTGSRTYSL
VGQAWPGPLADMAPTRKDKLLQFYPSLEDPASSRYQNFSKGSRHGSEEAYIDPIAMEYYN
WGRFSKPPEDDDANSYENVLICKQKTTETGAQQEGIGGLCRGDLSLSLALKTGPTSGLCP
SASPEEDEESEDYQNSASIHQWRESRKVMGQLQREASPGPVGSPDEEDGEPDYVNGEVAA
TEA
NT seq
732 nt
NT seq
+upstream
nt +downstream
nt
atgagctcggggactgaactgctgtggcccggagcagcgctgctggtgctgttgggggtg
gcagccagtctgtgtgtgcgctgctcacgcccaggtgcaaagaggtcagagaaaatctac
cagcagagaagtctgcgtgaggaccaacagagctttacggggtcccggacctactccttg
gtcgggcaggcatggccaggacccctggcggacatggcacccacaaggaaggacaagctg
ttgcaattctaccccagcctggaggatccagcatcttccaggtaccagaacttcagcaaa
ggaagcagacacgggtcggaggaagcctacatagaccccattgccatggagtattacaac
tgggggcggttctcgaagcccccagaagatgatgatgccaattcctacgagaatgtgctc
atttgcaagcagaaaaccacagagacaggtgcccagcaggagggcataggtggcctctgc
agaggggacctcagcctgtcactggccctgaagactggccccacttctggtctctgtccc
tctgcctccccggaagaagatgaggaatctgaggattatcagaactcagcatccatccat
cagtggcgcgagtccaggaaggtcatggggcaactccagagagaagcatcccctggcccg
gtgggaagcccagacgaggaggacggggaaccggattacgtgaatggggaggtggcagcc
acagaagcctag
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integrated database retrieval system
