Pteropus alecto (black flying fox): 102879561
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Entry
102879561 CDS
T02993
Gene name
FAS
Definition
(RefSeq) tumor necrosis factor receptor superfamily member 6 isoform X5
KO
K04390
tumor necrosis factor receptor superfamily member 6
Organism
pale
Pteropus alecto (black flying fox)
Pathway
pale01524
Platinum drug resistance
pale04010
MAPK signaling pathway
pale04060
Cytokine-cytokine receptor interaction
pale04115
p53 signaling pathway
pale04210
Apoptosis
pale04217
Necroptosis
pale04650
Natural killer cell mediated cytotoxicity
pale04668
TNF signaling pathway
pale04932
Non-alcoholic fatty liver disease
pale04940
Type I diabetes mellitus
pale05010
Alzheimer disease
pale05022
Pathways of neurodegeneration - multiple diseases
pale05142
Chagas disease
pale05143
African trypanosomiasis
pale05160
Hepatitis C
pale05161
Hepatitis B
pale05162
Measles
pale05163
Human cytomegalovirus infection
pale05164
Influenza A
pale05165
Human papillomavirus infection
pale05167
Kaposi sarcoma-associated herpesvirus infection
pale05168
Herpes simplex virus 1 infection
pale05169
Epstein-Barr virus infection
pale05170
Human immunodeficiency virus 1 infection
pale05200
Pathways in cancer
pale05205
Proteoglycans in cancer
pale05320
Autoimmune thyroid disease
pale05330
Allograft rejection
pale05332
Graft-versus-host disease
Brite
KEGG Orthology (KO) [BR:
pale00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
102879561 (FAS)
04668 TNF signaling pathway
102879561 (FAS)
09133 Signaling molecules and interaction
04060 Cytokine-cytokine receptor interaction
102879561 (FAS)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
102879561 (FAS)
04217 Necroptosis
102879561 (FAS)
04115 p53 signaling pathway
102879561 (FAS)
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
102879561 (FAS)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102879561 (FAS)
05205 Proteoglycans in cancer
102879561 (FAS)
09163 Immune disease
05320 Autoimmune thyroid disease
102879561 (FAS)
05330 Allograft rejection
102879561 (FAS)
05332 Graft-versus-host disease
102879561 (FAS)
09164 Neurodegenerative disease
05010 Alzheimer disease
102879561 (FAS)
05022 Pathways of neurodegeneration - multiple diseases
102879561 (FAS)
09167 Endocrine and metabolic disease
04940 Type I diabetes mellitus
102879561 (FAS)
04932 Non-alcoholic fatty liver disease
102879561 (FAS)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
102879561 (FAS)
05161 Hepatitis B
102879561 (FAS)
05160 Hepatitis C
102879561 (FAS)
05164 Influenza A
102879561 (FAS)
05162 Measles
102879561 (FAS)
05168 Herpes simplex virus 1 infection
102879561 (FAS)
05163 Human cytomegalovirus infection
102879561 (FAS)
05167 Kaposi sarcoma-associated herpesvirus infection
102879561 (FAS)
05169 Epstein-Barr virus infection
102879561 (FAS)
05165 Human papillomavirus infection
102879561 (FAS)
09174 Infectious disease: parasitic
05142 Chagas disease
102879561 (FAS)
05143 African trypanosomiasis
102879561 (FAS)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
102879561 (FAS)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04050 Cytokine receptors [BR:
pale04050
]
102879561 (FAS)
04090 CD molecules [BR:
pale04090
]
102879561 (FAS)
Cytokine receptors [BR:
pale04050
]
Tumor necrosis factor receptors
TNF receptor superfamily
102879561 (FAS)
CD molecules [BR:
pale04090
]
Proteins
102879561 (FAS)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Death
TNFR_c6
Stn1_C
DciA
Motif
Other DBs
NCBI-GeneID:
102879561
NCBI-ProteinID:
XP_006926030
LinkDB
All DBs
Position
Unknown
AA seq
335 aa
AA seq
DB search
MTGLGVLLPLIVIFIAGPLSKGGNTQVTSINSEVLESSHNITERESGCPKGLHRDGKFCC
HLCPPGTRKDTGCTTDEGKPDCVPCPEGEEYTDRKHYSSKCRRCGICDGEQGLEVEKNCT
QIQNTQCRCKSNFFCDIPPCEHCNPCDTCEHGISENCTPTNNTKCKVFQSTGSSRGYLWF
LIFIPISALAGSVIWWRKRRGRNNVGHNESRASIPRIVPMNFSDIDLSKYITTIAEQMKI
NQVREFVRKNGINEAKIDEIKNDNLQDTAEQKVQLLRNWYQLHGKKDAYCTLIQSLKKAN
LYVLAEKIEDIVQKDMVSEHENANIRNENESQSLV
NT seq
1008 nt
NT seq
+upstream
nt +downstream
nt
atgaccgggctcggggttctcctgcctctgatagttatctttattgctggaccattatct
aaaggtggtaatacccaagtgaccagtatcaactctgaggtgttggaatcaagtcataac
attactgaacgggagtctgggtgcccgaaaggcctacatcgtgatggtaaattctgctgt
cacctatgtcctcctggcacacggaaagatactggttgtacaactgatgagggcaaacca
gactgtgttccctgtccagaaggagaggagtacacagacaggaaacattattcttctaaa
tgcagaagatgtggaatttgtgatggagaacaaggcttagaagtggaaaaaaactgtacc
cagatccagaatacccagtgcagatgtaaatcaaactttttttgtgacattcctccatgc
gagcactgtaatccttgcgatacgtgtgaacatggaatcagtgagaattgcacaccaacc
aacaacaccaaatgtaaagtgttccaatctacaggatccagccgtgggtatctgtggttc
ctcatcttcatcccgatttcagcacttgcaggatcagtaatttggtggcggaaaagacga
ggcaggaataatgttggtcacaatgaatctagagcttcaattcctagaatagttccaatg
aatttctcagacatcgacttgagtaaatatattaccactattgctgagcaaatgaaaata
aatcaagttagagaattcgttcggaagaatggtatcaatgaagcaaaaatagatgaaatc
aagaatgacaatctccaagatacagctgaacagaaggtccagctgctccgtaattggtat
caacttcacgggaagaaagatgcatattgcactttgattcaaagtctcaagaaagccaat
ctttatgtccttgcagagaaaattgaagatatagtccaaaaggacatggttagtgaacat
gaaaatgctaacatcagaaatgaaaatgaaagccaaagcttggtctaa
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