Ailuropoda melanoleuca (giant panda): 100473767
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Entry
100473767 CDS
T01329
Gene name
FAS
Definition
(RefSeq) tumor necrosis factor receptor superfamily member 6
KO
K04390
tumor necrosis factor receptor superfamily member 6
Organism
aml
Ailuropoda melanoleuca (giant panda)
Pathway
aml01524
Platinum drug resistance
aml04010
MAPK signaling pathway
aml04060
Cytokine-cytokine receptor interaction
aml04115
p53 signaling pathway
aml04210
Apoptosis
aml04217
Necroptosis
aml04650
Natural killer cell mediated cytotoxicity
aml04668
TNF signaling pathway
aml04932
Non-alcoholic fatty liver disease
aml04940
Type I diabetes mellitus
aml05010
Alzheimer disease
aml05022
Pathways of neurodegeneration - multiple diseases
aml05142
Chagas disease
aml05143
African trypanosomiasis
aml05160
Hepatitis C
aml05161
Hepatitis B
aml05162
Measles
aml05163
Human cytomegalovirus infection
aml05164
Influenza A
aml05165
Human papillomavirus infection
aml05167
Kaposi sarcoma-associated herpesvirus infection
aml05168
Herpes simplex virus 1 infection
aml05169
Epstein-Barr virus infection
aml05170
Human immunodeficiency virus 1 infection
aml05200
Pathways in cancer
aml05205
Proteoglycans in cancer
aml05320
Autoimmune thyroid disease
aml05330
Allograft rejection
aml05332
Graft-versus-host disease
Brite
KEGG Orthology (KO) [BR:
aml00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
100473767 (FAS)
04668 TNF signaling pathway
100473767 (FAS)
09133 Signaling molecules and interaction
04060 Cytokine-cytokine receptor interaction
100473767 (FAS)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
100473767 (FAS)
04217 Necroptosis
100473767 (FAS)
04115 p53 signaling pathway
100473767 (FAS)
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
100473767 (FAS)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100473767 (FAS)
05205 Proteoglycans in cancer
100473767 (FAS)
09163 Immune disease
05320 Autoimmune thyroid disease
100473767 (FAS)
05330 Allograft rejection
100473767 (FAS)
05332 Graft-versus-host disease
100473767 (FAS)
09164 Neurodegenerative disease
05010 Alzheimer disease
100473767 (FAS)
05022 Pathways of neurodegeneration - multiple diseases
100473767 (FAS)
09167 Endocrine and metabolic disease
04940 Type I diabetes mellitus
100473767 (FAS)
04932 Non-alcoholic fatty liver disease
100473767 (FAS)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100473767 (FAS)
05161 Hepatitis B
100473767 (FAS)
05160 Hepatitis C
100473767 (FAS)
05164 Influenza A
100473767 (FAS)
05162 Measles
100473767 (FAS)
05168 Herpes simplex virus 1 infection
100473767 (FAS)
05163 Human cytomegalovirus infection
100473767 (FAS)
05167 Kaposi sarcoma-associated herpesvirus infection
100473767 (FAS)
05169 Epstein-Barr virus infection
100473767 (FAS)
05165 Human papillomavirus infection
100473767 (FAS)
09174 Infectious disease: parasitic
05142 Chagas disease
100473767 (FAS)
05143 African trypanosomiasis
100473767 (FAS)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100473767 (FAS)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04050 Cytokine receptors [BR:
aml04050
]
100473767 (FAS)
04090 CD molecules [BR:
aml04090
]
100473767 (FAS)
Cytokine receptors [BR:
aml04050
]
Tumor necrosis factor receptors
TNF receptor superfamily
100473767 (FAS)
CD molecules [BR:
aml04090
]
Proteins
100473767 (FAS)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Death
TNFR_c6
CcmH
SIT
Stn1_C
Motif
Other DBs
NCBI-GeneID:
100473767
NCBI-ProteinID:
XP_034518293
LinkDB
All DBs
Position
6
AA seq
371 aa
AA seq
DB search
MGTGPEFRAPCWDRVSAARPPRAEGDAFIPVSQRAGWRPASSSSSRAPAARLSGRAGTSV
RPISKVQILTSIARPWPKGVNAQATAIDSRLLRVRKNITIRETGCPEGLHRGDTFCCQPC
PPGTRKEGDCKSERGESICVLCQEGVEYTEEKHFSDKCRRCTLCDGEHGLEVEKNCTRTQ
NTKCRCKPNFFCNVSECGHCTPCTTCEHGILESCTPTSNTKCKEGSSSKFLWFCVLIPIL
IAALICWWMLRRRRKKSHEVRRSTGSATEMMPINFADIDLSKYITSVSEQMTITQVREFV
RKNGINEAKIDEIKNDNLQDTAEQKVQLLRNWYQLHGKKDAYCNLIRGLRKANFCALAER
IEEMIQRDITS
NT seq
1116 nt
NT seq
+upstream
nt +downstream
nt
atggggaccggccctgagttccgcgcaccgtgctgggaccgtgtgtcagcggcgcgcccg
ccgcgggctgagggcgatgccttcatccccgtttcacagagggccggatggaggccggca
agctcaagtagcagccgagctcccgcagcgcgtctaagtggcagagctgggacttcagtt
agacctatttccaaagtccagatacttacctccatcgcccgaccgtggcctaaaggtgtc
aatgctcaagcaactgccatcgattccaggctgttgagagtgcggaagaacattaccata
agggagacggggtgcccggaaggcctgcatcgtggggacacgttctgctgtcagccgtgt
cctcctggcacacggaaagagggcgactgcaagtctgagaggggtgaatcaatatgtgtg
ctctgccaggaaggggtggagtacacggaggagaagcatttttctgataaatgcagaaga
tgcacactttgcgatggagagcatggcttggaagtggaaaaaaactgtacccggacccag
aataccaagtgcaggtgtaaaccaaactttttttgtaacgtctctgaatgcggacactgt
accccgtgcaccacgtgtgaacacggaatccttgagagttgcacaccaaccagcaatacc
aaatgcaaagaaggatccagctccaaatttctgtggttttgtgtcctaatcccgattctt
atagctgcactaatatgttggtggatgttaagacggcgcaggaagaaaagccatgaagtc
cgtcgatccacaggctcagccactgaaatgatgccaataaattttgcagacatcgacctg
agtaaatatatcactagtgtttctgaacaaatgacaataactcaagtcagagaatttgtt
cggaagaatggtatcaacgaagccaagatagatgagatcaagaatgacaatctccaagac
acagcggaacagaaagtccagttgctccgtaattggtatcaactccacgggaagaaagat
gcatattgcaatttaattagaggcctcagaaaagccaatttttgtgcactagcagagaga
attgaagaaatgatccagagggacattactagctaa
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