Heterocephalus glaber (naked mole-rat): 101698980
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Entry
101698980 CDS
T02812
Symbol
Tnfrsf1a
Name
(RefSeq) TNF receptor superfamily member 1A
KO
K03158
tumor necrosis factor receptor superfamily member 1A
Organism
hgl
Heterocephalus glaber (naked mole-rat)
Pathway
hgl04010
MAPK signaling pathway
hgl04060
Cytokine-cytokine receptor interaction
hgl04061
Viral protein interaction with cytokine and cytokine receptor
hgl04064
NF-kappa B signaling pathway
hgl04071
Sphingolipid signaling pathway
hgl04150
mTOR signaling pathway
hgl04210
Apoptosis
hgl04215
Apoptosis - multiple species
hgl04217
Necroptosis
hgl04380
Osteoclast differentiation
hgl04668
TNF signaling pathway
hgl04920
Adipocytokine signaling pathway
hgl04931
Insulin resistance
hgl04932
Non-alcoholic fatty liver disease
hgl04936
Alcoholic liver disease
hgl05010
Alzheimer disease
hgl05014
Amyotrophic lateral sclerosis
hgl05022
Pathways of neurodegeneration - multiple diseases
hgl05132
Salmonella infection
hgl05142
Chagas disease
hgl05145
Toxoplasmosis
hgl05152
Tuberculosis
hgl05160
Hepatitis C
hgl05163
Human cytomegalovirus infection
hgl05164
Influenza A
hgl05165
Human papillomavirus infection
hgl05166
Human T-cell leukemia virus 1 infection
hgl05167
Kaposi sarcoma-associated herpesvirus infection
hgl05168
Herpes simplex virus 1 infection
hgl05170
Human immunodeficiency virus 1 infection
hgl05171
Coronavirus disease - COVID-19
hgl05417
Lipid and atherosclerosis
hgl05418
Fluid shear stress and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
hgl00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
101698980 (Tnfrsf1a)
04064 NF-kappa B signaling pathway
101698980 (Tnfrsf1a)
04668 TNF signaling pathway
101698980 (Tnfrsf1a)
04071 Sphingolipid signaling pathway
101698980 (Tnfrsf1a)
04150 mTOR signaling pathway
101698980 (Tnfrsf1a)
09133 Signaling molecules and interaction
04060 Cytokine-cytokine receptor interaction
101698980 (Tnfrsf1a)
04061 Viral protein interaction with cytokine and cytokine receptor
101698980 (Tnfrsf1a)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
101698980 (Tnfrsf1a)
04215 Apoptosis - multiple species
101698980 (Tnfrsf1a)
04217 Necroptosis
101698980 (Tnfrsf1a)
09150 Organismal Systems
09152 Endocrine system
04920 Adipocytokine signaling pathway
101698980 (Tnfrsf1a)
09158 Development and regeneration
04380 Osteoclast differentiation
101698980 (Tnfrsf1a)
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
101698980 (Tnfrsf1a)
05170 Human immunodeficiency virus 1 infection
101698980 (Tnfrsf1a)
05160 Hepatitis C
101698980 (Tnfrsf1a)
05171 Coronavirus disease - COVID-19
101698980 (Tnfrsf1a)
05164 Influenza A
101698980 (Tnfrsf1a)
05168 Herpes simplex virus 1 infection
101698980 (Tnfrsf1a)
05163 Human cytomegalovirus infection
101698980 (Tnfrsf1a)
05167 Kaposi sarcoma-associated herpesvirus infection
101698980 (Tnfrsf1a)
05165 Human papillomavirus infection
101698980 (Tnfrsf1a)
09171 Infectious disease: bacterial
05132 Salmonella infection
101698980 (Tnfrsf1a)
05152 Tuberculosis
101698980 (Tnfrsf1a)
09174 Infectious disease: parasitic
05145 Toxoplasmosis
101698980 (Tnfrsf1a)
05142 Chagas disease
101698980 (Tnfrsf1a)
09164 Neurodegenerative disease
05010 Alzheimer disease
101698980 (Tnfrsf1a)
05014 Amyotrophic lateral sclerosis
101698980 (Tnfrsf1a)
05022 Pathways of neurodegeneration - multiple diseases
101698980 (Tnfrsf1a)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
101698980 (Tnfrsf1a)
05418 Fluid shear stress and atherosclerosis
101698980 (Tnfrsf1a)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
101698980 (Tnfrsf1a)
04932 Non-alcoholic fatty liver disease
101698980 (Tnfrsf1a)
04931 Insulin resistance
101698980 (Tnfrsf1a)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04050 Cytokine receptors [BR:
hgl04050
]
101698980 (Tnfrsf1a)
04090 CD molecules [BR:
hgl04090
]
101698980 (Tnfrsf1a)
Cytokine receptors [BR:
hgl04050
]
Tumor necrosis factor receptors
TNF receptor superfamily
101698980 (Tnfrsf1a)
CD molecules [BR:
hgl04090
]
Proteins
101698980 (Tnfrsf1a)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Death
TNFR_c6
Motif
Other DBs
NCBI-GeneID:
101698980
NCBI-ProteinID:
XP_004869439
UniProt:
A0AAX6Q8C5
LinkDB
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Position
Un
AA seq
461 aa
AA seq
DB search
MGLPTVPGPLLPLVLLALLVGIHSSGVIGLVPSFGDREKRESPCPQGKYSHPQNNSICCT
KCHKGTYLHNDCLGPGLDTDCRECASGTFTSTENHSPVCLTCSSCRKELLQVELSPCTVD
QDTVCGCRKNQFRNYYGETYFRCTDCSQCLNGTVTIRCQERQNTVCLCHTGFFLRGSKCV
SCSECKQDSECTKLCPHPVVRPPQDSGTTVLLPLVILLGLCLLSLLFIVLMCRYPRWKPK
LYSIVCGTSAPVKEGELEGITSTKPLAPTPGFSPTASCRLPPSSPSPPRGPGDFRDVAAP
PLGAEPIFAPGLTAAPVPRAGHGHNGEDGADSQGGRWPAAGPEPATLYAVVDGVPPSRWK
EFMRRLGLGEHEIERLELQNGRCLREAHYSMLAAWRQRTPPHEATLDLLGRVLCDMDLLG
CLEDIRDTLRGRACEALPSSGPAPIGAPSRGLRLSLTRDAL
NT seq
1386 nt
NT seq
+upstream
nt +downstream
nt
atgggcctccccaccgtgcctggcccgctgctgccactggtgctcctggctctgctggtg
gggatacattcatcaggtgtcattggcctggtcccttcctttggggatcgggagaagagg
gagagtccgtgtccccagggaaaatacagccaccctcaaaacaattccatctgctgcacc
aagtgccacaaagggacctacttgcacaatgactgcctgggccccgggctggacacggac
tgcagggagtgtgcaagcggcaccttcacctccactgagaaccactcccctgtgtgcctc
acctgctccagctgtcggaaagaactgctccaggtggagctttctccttgcacagtggac
caggacactgtgtgtggctgcaggaagaaccagttccggaactattatggggaaacatat
ttccggtgcacggactgcagccagtgcctcaatggcaccgtgacgatccgatgccaggag
agacagaacactgtgtgcctctgccacacaggcttctttctgagaggcagcaagtgtgtc
tcttgcagcgaatgtaagcaagactcggagtgcacgaagttgtgcccacaccctgtagtt
aggcccccccaggactcaggtaccacagtgctgttgcccctggtgatcctgttaggcctt
tgccttttatctttgctcttcatcgttttaatgtgccgctatccaaggtggaagccgaag
ctctactctattgtttgtgggacatcagcacccgtgaaagagggcgagctggaaggaatt
acgtccactaagcccctcgccccgaccccgggtttcagccccacggccagctgcaggctg
ccccccagctctccctcccctccgaggggccctggggacttcagggacgtcgctgcccca
cccctgggggctgagcccatcttcgccccggggctcacggcggcgcccgtccccagggcc
ggccatggccacaacggggaagacggcgccgacagccaaggagggcgctggccggccgca
ggccccgagcccgcaacgctgtacgccgtggtggacggcgtgcctccgtcccgctggaag
gagttcatgcgacgcctggggctgggcgagcatgagatcgagcggctggagctgcagaac
gggcgctgcctgcgcgaggcgcactacagcatgctggcagcctggcggcagcgcaccccg
ccacacgaggccacgctggacctgctgggccgcgtgctgtgcgacatggacctcctgggc
tgcctggaggacatccgggacacgctgcgggggcgggcatgcgaggccctgccctccagt
ggccctgcaccaattggggcgccttctcggggcctccgactaagcctgacgcgcgatgcc
ctgtga
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