KEGG   Homo sapiens (human): 8764
Entry
8764              CDS       T01001                                 
Symbol
TNFRSF14, ATAR, CD270, HVEA, HVEM, LIGHTR, TR2
Name
(RefSeq) TNF receptor superfamily member 14
  KO
K05152  tumor necrosis factor receptor superfamily member 14
Organism
hsa  Homo sapiens (human)
Pathway
hsa03266  Virion - Herpesvirus
hsa04060  Cytokine-cytokine receptor interaction
hsa04061  Viral protein interaction with cytokine and cytokine receptor
hsa05168  Herpes simplex virus 1 infection
Network
nt06168  Herpes simplex virus 1 (HSV-1)
nt06516  TNF signaling
  Element
N00559  LIGHT-HVEM-NFKB signaling pathway
N00560  HSV gD to HVEM-NFKB signaling pathway
Disease
H02434  Diffuse large B-cell lymphoma, not otherwise specified
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03266 Virion - Herpesvirus
    8764 (TNFRSF14)
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04060 Cytokine-cytokine receptor interaction
    8764 (TNFRSF14)
   04061 Viral protein interaction with cytokine and cytokine receptor
    8764 (TNFRSF14)
 09160 Human Diseases
  09172 Infectious disease: viral
   05168 Herpes simplex virus 1 infection
    8764 (TNFRSF14)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04050 Cytokine receptors [BR:hsa04050]
    8764 (TNFRSF14)
   04090 CD molecules [BR:hsa04090]
    8764 (TNFRSF14)
Cytokine receptors [BR:hsa04050]
 Tumor necrosis factor receptors
  TNF receptor superfamily
   8764 (TNFRSF14)
CD molecules [BR:hsa04090]
 Proteins
  8764 (TNFRSF14)
SSDB
Motif
Pfam: TNFR_c6 Hum_adeno_E3A MHYT Peptidase_U4
Other DBs
NCBI-GeneID: 8764
NCBI-ProteinID: NP_003811
OMIM: 602746
HGNC: 11912
Ensembl: ENSG00000157873
Pharos: Q92956(Tbio)
UniProt: Q92956
Structure
LinkDB
Position
1:2554234..2563829
AA seq 283 aa
MEPPGDWGPPPWRSTPKTDVLRLVLYLTFLGAPCYAPALPSCKEDEYPVGSECCPKCSPG
YRVKEACGELTGTVCEPCPPGTYIAHLNGLSKCLQCQMCDPAMGLRASRNCSRTENAVCG
CSPGHFCIVQDGDHCAACRAYATSSPGQRVQKGGTESQDTLCQNCPPGTFSPNGTLEECQ
HQTKCSWLVTKAGAGTSSSHWVWWFLSGSLVIVIVCSTVGLIICVKRRKPRGDVVKVIVS
VQRKRQEAEGEATVIEALQAPPDVTTVAVEETIPSFTGRSPNH
NT seq 852 nt   +upstreamnt  +downstreamnt
atggagcctcctggagactgggggcctcctccctggagatccacccccaaaaccgacgtc
ttgaggctggtgctgtatctcaccttcctgggagccccctgctacgccccagctctgccg
tcctgcaaggaggacgagtacccagtgggctccgagtgctgccccaagtgcagtccaggt
tatcgtgtgaaggaggcctgcggggagctgacgggcacagtgtgtgaaccctgccctcca
ggcacctacattgcccacctcaatggcctaagcaagtgtctgcagtgccaaatgtgtgac
ccagccatgggcctgcgcgcgagccggaactgctccaggacagagaacgccgtgtgtggc
tgcagcccaggccacttctgcatcgtccaggacggggaccactgcgccgcgtgccgcgct
tacgccacctccagcccgggccagagggtgcagaagggaggcaccgagagtcaggacacc
ctgtgtcagaactgccccccggggaccttctctcccaatgggaccctggaggaatgtcag
caccagaccaagtgcagctggctggtgacgaaggccggagctgggaccagcagctcccac
tgggtatggtggtttctctcagggagcctcgtcatcgtcattgtttgctccacagttggc
ctaatcatatgtgtgaaaagaagaaagccaaggggtgatgtagtcaaggtgatcgtctcc
gtccagcggaaaagacaggaggcagaaggtgaggccacagtcattgaggccctgcaggcc
cctccggacgtcaccacggtggccgtggaggagacaataccctcattcacggggaggagc
ccaaaccactga

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