Homo sapiens (human): 2353
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Entry
2353 CDS
T01001
Symbol
FOS, AP-1, C-FOS, p55
Name
(RefSeq) Fos proto-oncogene, AP-1 transcription factor subunit
KO
K04379
proto-oncogene protein c-fos
Organism
hsa
Homo sapiens (human)
Pathway
hsa01522
Endocrine resistance
hsa04010
MAPK signaling pathway
hsa04024
cAMP signaling pathway
hsa04210
Apoptosis
hsa04380
Osteoclast differentiation
hsa04620
Toll-like receptor signaling pathway
hsa04657
IL-17 signaling pathway
hsa04658
Th1 and Th2 cell differentiation
hsa04659
Th17 cell differentiation
hsa04660
T cell receptor signaling pathway
hsa04662
B cell receptor signaling pathway
hsa04668
TNF signaling pathway
hsa04713
Circadian entrainment
hsa04725
Cholinergic synapse
hsa04728
Dopaminergic synapse
hsa04915
Estrogen signaling pathway
hsa04917
Prolactin signaling pathway
hsa04921
Oxytocin signaling pathway
hsa04926
Relaxin signaling pathway
hsa04928
Parathyroid hormone synthesis, secretion and action
hsa04932
Non-alcoholic fatty liver disease
hsa04935
Growth hormone synthesis, secretion and action
hsa05031
Amphetamine addiction
hsa05130
Pathogenic Escherichia coli infection
hsa05132
Salmonella infection
hsa05133
Pertussis
hsa05135
Yersinia infection
hsa05140
Leishmaniasis
hsa05142
Chagas disease
hsa05161
Hepatitis B
hsa05162
Measles
hsa05166
Human T-cell leukemia virus 1 infection
hsa05167
Kaposi sarcoma-associated herpesvirus infection
hsa05170
Human immunodeficiency virus 1 infection
hsa05171
Coronavirus disease - COVID-19
hsa05200
Pathways in cancer
hsa05207
Chemical carcinogenesis - receptor activation
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05210
Colorectal cancer
hsa05224
Breast cancer
hsa05231
Choline metabolism in cancer
hsa05235
PD-L1 expression and PD-1 checkpoint pathway in cancer
hsa05323
Rheumatoid arthritis
hsa05417
Lipid and atherosclerosis
hsa05418
Fluid shear stress and atherosclerosis
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06162
Hepatitis B virus (HBV)
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06180
Pathogenic Escherichia coli
nt06181
Salmonella
nt06182
Shigella
nt06183
Yersinia
nt06210
ERK signaling (cancer)
nt06211
Other MAPK signaling (cancer)
nt06214
PI3K signaling (cancer)
nt06223
TNF signaling (cancer)
nt06263
Hepatocellular carcinoma
nt06461
Huntington disease
nt06516
TNF signaling
nt06517
TLR signaling
nt06526
MAPK signaling
Element
N00188
IL1-IL1R-JNK signaling pathway
N00438
TLR2/4-MAPK signaling pathway
N00446
TNF-JNK signaling pathway
N00447
HIV Vpr/Tat to TNF-JNK signaling pathway
N00509
HTLV-1 Tax to SRF-mediated transcription
N00545
HBV HBx to ERK signaling pathway
N01344
NNK/NNN to RAS-ERK signaling pathway
N01350
NNK/NNN to PI3K signaling pathway
N01353
E2 to RAS-ERK signaling pathway
N01407
Metals to JNK signaling pathway
N01408
Metals to RAS-ERK signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
2353 (FOS)
04668 TNF signaling pathway
2353 (FOS)
04024 cAMP signaling pathway
2353 (FOS)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
2353 (FOS)
09150 Organismal Systems
09151 Immune system
04620 Toll-like receptor signaling pathway
2353 (FOS)
04660 T cell receptor signaling pathway
2353 (FOS)
04658 Th1 and Th2 cell differentiation
2353 (FOS)
04659 Th17 cell differentiation
2353 (FOS)
04657 IL-17 signaling pathway
2353 (FOS)
04662 B cell receptor signaling pathway
2353 (FOS)
09152 Endocrine system
04915 Estrogen signaling pathway
2353 (FOS)
04917 Prolactin signaling pathway
2353 (FOS)
04921 Oxytocin signaling pathway
2353 (FOS)
04926 Relaxin signaling pathway
2353 (FOS)
04935 Growth hormone synthesis, secretion and action
2353 (FOS)
04928 Parathyroid hormone synthesis, secretion and action
2353 (FOS)
09156 Nervous system
04725 Cholinergic synapse
2353 (FOS)
04728 Dopaminergic synapse
2353 (FOS)
09158 Development and regeneration
04380 Osteoclast differentiation
2353 (FOS)
09159 Environmental adaptation
04713 Circadian entrainment
2353 (FOS)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
2353 (FOS)
05207 Chemical carcinogenesis - receptor activation
2353 (FOS)
05208 Chemical carcinogenesis - reactive oxygen species
2353 (FOS)
05231 Choline metabolism in cancer
2353 (FOS)
05235 PD-L1 expression and PD-1 checkpoint pathway in cancer
2353 (FOS)
09162 Cancer: specific types
05210 Colorectal cancer
2353 (FOS)
05224 Breast cancer
2353 (FOS)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
2353 (FOS)
05170 Human immunodeficiency virus 1 infection
2353 (FOS)
05161 Hepatitis B
2353 (FOS)
05171 Coronavirus disease - COVID-19
2353 (FOS)
05162 Measles
2353 (FOS)
05167 Kaposi sarcoma-associated herpesvirus infection
2353 (FOS)
09171 Infectious disease: bacterial
05130 Pathogenic Escherichia coli infection
2353 (FOS)
05132 Salmonella infection
2353 (FOS)
05135 Yersinia infection
2353 (FOS)
05133 Pertussis
2353 (FOS)
09174 Infectious disease: parasitic
05140 Leishmaniasis
2353 (FOS)
05142 Chagas disease
2353 (FOS)
09163 Immune disease
05323 Rheumatoid arthritis
2353 (FOS)
09165 Substance dependence
05031 Amphetamine addiction
2353 (FOS)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
2353 (FOS)
05418 Fluid shear stress and atherosclerosis
2353 (FOS)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
2353 (FOS)
09176 Drug resistance: antineoplastic
01522 Endocrine resistance
2353 (FOS)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
2353 (FOS)
04131 Membrane trafficking [BR:
hsa04131
]
2353 (FOS)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic leucine zipper (bZIP)
AP-1(-like) components, Fos
2353 (FOS)
Membrane trafficking [BR:
hsa04131
]
Autophagy
Chaperone mediated autophagy (CMA)
Selective cargos
2353 (FOS)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
bZIP_1
bZIP_2
bZIP_Maf
MIC19_MIC25
DUF3450
HALZ
Macoilin
Motif
Other DBs
NCBI-GeneID:
2353
NCBI-ProteinID:
NP_005243
OMIM:
164810
HGNC:
3796
Ensembl:
ENSG00000170345
UniProt:
P01100
Q6FG41
Structure
PDB
LinkDB
All DBs
Position
14:75278828..75282230
Genome browser
AA seq
380 aa
AA seq
DB search
MMFSGFNADYEASSSRCSSASPAGDSLSYYHSPADSFSSMGSPVNAQDFCTDLAVSSANF
IPTVTAISTSPDLQWLVQPALVSSVAPSQTRAPHPFGVPAPSAGAYSRAGVVKTMTGGRA
QSIGRRGKVEQLSPEEEEKRRIRRERNKMAAAKCRNRRRELTDTLQAETDQLEDEKSALQ
TEIANLLKEKEKLEFILAAHRPACKIPDDLGFPEEMSVASLDLTGGLPEVATPESEEAFT
LPLLNDPEPKPSVEPVKSISSMELKTEPFDDFLFPASSRPSGSETARSVPDMDLSGSFYA
ADWEPLHSGSLGMGPMATELEPLCTPVVTCTPSCTAYTSSFVFTYPEADSFPSCAAAHRK
GSSSNEPSSDSLSSPTLLAL
NT seq
1143 nt
NT seq
+upstream
nt +downstream
nt
atgatgttctcgggcttcaacgcagactacgaggcgtcatcctcccgctgcagcagcgcg
tccccggccggggatagcctctcttactaccactcacccgcagactccttctccagcatg
ggctcgcctgtcaacgcgcaggacttctgcacggacctggccgtctccagtgccaacttc
attcccacggtcactgccatctcgaccagtccggacctgcagtggctggtgcagcccgcc
ctcgtctcctccgtggccccatcgcagaccagagcccctcaccctttcggagtccccgcc
ccctccgctggggcttactccagggctggcgttgtgaagaccatgacaggaggccgagcg
cagagcattggcaggaggggcaaggtggaacagttatctccagaagaagaagagaaaagg
agaatccgaagggaaaggaataagatggctgcagccaaatgccgcaaccggaggagggag
ctgactgatacactccaagcggagacagaccaactagaagatgagaagtctgctttgcag
accgagattgccaacctgctgaaggagaaggaaaaactagagttcatcctggcagctcac
cgacctgcctgcaagatccctgatgacctgggcttcccagaagagatgtctgtggcttcc
cttgatctgactgggggcctgccagaggttgccaccccggagtctgaggaggccttcacc
ctgcctctcctcaatgaccctgagcccaagccctcagtggaacctgtcaagagcatcagc
agcatggagctgaagaccgagccctttgatgacttcctgttcccagcatcatccaggccc
agtggctctgagacagcccgctccgtgccagacatggacctatctgggtccttctatgca
gcagactgggagcctctgcacagtggctccctggggatggggcccatggccacagagctg
gagcccctgtgcactccggtggtcacctgtactcccagctgcactgcttacacgtcttcc
ttcgtcttcacctaccccgaggctgactccttccccagctgtgcagctgcccaccgcaag
ggcagcagcagcaatgagccttcctctgactcgctcagctcacccacgctgctggccctg
tga
Homo sapiens (human): 8061
Help
Entry
8061 CDS
T01001
Symbol
FOSL1, FRA, FRA1, fra-1
Name
(RefSeq) FOS like 1, AP-1 transcription factor subunit
KO
K04502
fos-like antigen 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04310
Wnt signaling pathway
hsa04380
Osteoclast differentiation
hsa04657
IL-17 signaling pathway
hsa05166
Human T-cell leukemia virus 1 infection
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
Element
N00509
HTLV-1 Tax to SRF-mediated transcription
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
8061 (FOSL1)
09150 Organismal Systems
09151 Immune system
04657 IL-17 signaling pathway
8061 (FOSL1)
09158 Development and regeneration
04380 Osteoclast differentiation
8061 (FOSL1)
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
8061 (FOSL1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
8061 (FOSL1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic leucine zipper (bZIP)
AP-1(-like) components, Fos
8061 (FOSL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
bZIP_1
bZIP_Maf
bZIP_2
DUF3450
MYO10_CC
DUF4407
DUF4527
DUF4606
Macoilin
Motif
Other DBs
NCBI-GeneID:
8061
NCBI-ProteinID:
NP_005429
OMIM:
136515
HGNC:
13718
Ensembl:
ENSG00000175592
UniProt:
P15407
A0A0S2Z595
LinkDB
All DBs
Position
11:complement(65892049..65900545)
Genome browser
AA seq
271 aa
AA seq
DB search
MFRDFGEPGPSSGNGGGYGGPAQPPAAAQAAQQKFHLVPSINTMSGSQELQWMVQPHFLG
PSSYPRPLTYPQYSPPQPRPGVIRALGPPPGVRRRPCEQISPEEEERRRVRRERNKLAAA
KCRNRRKELTDFLQAETDKLEDEKSGLQREIEELQKQKERLELVLEAHRPICKIPEGAKE
GDTGSTSGTSSPPAPCRPVPCISLSPGPVLEPEALHTPTLMTTPSLTPFTPSLVFTYPST
PEPCASAHRKSSSSSGDPSSDPLGSPTLLAL
NT seq
816 nt
NT seq
+upstream
nt +downstream
nt
atgttccgagacttcggggaacccggcccgagctccgggaacggcggcgggtacggcggc
cccgcgcagcccccggccgcagcgcaggcagcccagcagaagttccacctggtgccaagc
atcaacaccatgagtggcagtcaggagctgcagtggatggtacagcctcatttcctgggg
cccagcagttaccccaggcctctgacctaccctcagtacagccccccacaaccccggcca
ggagtcatccgggccctggggccgcctccaggggtacgtcgaaggccttgtgaacagatc
agcccggaggaagaggagcgccgccgagtaaggcgcgagcggaacaagctggctgcggcc
aagtgcaggaaccggaggaaggaactgaccgacttcctgcaggcggagactgacaaactg
gaagatgagaaatctgggctgcagcgagagattgaggagctgcagaagcagaaggagcgc
ctagagctggtgctggaagcccaccgacccatctgcaaaatcccggaaggagccaaggag
ggggacacaggcagtaccagtggcaccagcagcccaccagccccctgccgccctgtacct
tgtatctccctttccccagggcctgtgcttgaacctgaggcactgcacacccccacactc
atgaccacaccctccctaactcctttcacccccagcctggtcttcacctaccccagcact
cctgagccttgtgcctcagctcatcgcaagagtagcagcagcagcggagacccatcctct
gacccccttggctctccaaccctcctcgctttgtga
Homo sapiens (human): 1958
Help
Entry
1958 CDS
T01001
Symbol
EGR1, AT225, G0S30, KROX-24, NGFI-A, TIS8, ZIF-268, ZNF225
Name
(RefSeq) early growth response 1
KO
K09203
early growth response protein 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04371
Apelin signaling pathway
hsa04912
GnRH signaling pathway
hsa04928
Parathyroid hormone synthesis, secretion and action
hsa04933
AGE-RAGE signaling pathway in diabetic complications
hsa05020
Prion disease
hsa05166
Human T-cell leukemia virus 1 infection
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
nt06465
Prion disease
Element
N00509
HTLV-1 Tax to SRF-mediated transcription
N01204
PRNP-PI3K-NOX2 signaling pathway
Drug target
Brivoligide:
D11341
Brivoligide sodium:
D11286
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04371 Apelin signaling pathway
1958 (EGR1)
09150 Organismal Systems
09152 Endocrine system
04912 GnRH signaling pathway
1958 (EGR1)
04928 Parathyroid hormone synthesis, secretion and action
1958 (EGR1)
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
1958 (EGR1)
09164 Neurodegenerative disease
05020 Prion disease
1958 (EGR1)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
1958 (EGR1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
1958 (EGR1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 SP/KLF family and related proteins
1958 (EGR1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF3432
DUF3446
zf-H2C2_2
zf-C2H2
zf-C2H2_4
zf-C2HC_2
Cornifin
zf-BED
zf-H2C2_5
Motif
Other DBs
NCBI-GeneID:
1958
NCBI-ProteinID:
NP_001955
OMIM:
128990
HGNC:
3238
Ensembl:
ENSG00000120738
UniProt:
P18146
Q546S1
Structure
PDB
LinkDB
All DBs
Position
5:138465479..138469303
Genome browser
AA seq
543 aa
AA seq
DB search
MAAAKAEMQLMSPLQISDPFGSFPHSPTMDNYPKLEEMMLLSNGAPQFLGAAGAPEGSGS
NSSSSSSGGGGGGGGGSNSSSSSSTFNPQADTGEQPYEHLTAESFPDISLNNEKVLVETS
YPSQTTRLPPITYTGRFSLEPAPNSGNTLWPEPLFSLVSGLVSMTNPPASSSSAPSPAAS
SASASQSPPLSCAVPSNDSSPIYSAAPTFPTPNTDIFPEPQSQAFPGSAGTALQYPPPAY
PAAKGGFQVPMIPDYLFPQQQGDLGLGTPDQKPFQGLESRTQQPSLTPLSTIKAFATQSG
SQDLKALNTSYQSQLIKPSRMRKYPNRPSKTPPHERPYACPVESCDRRFSRSDELTRHIR
IHTGQKPFQCRICMRNFSRSDHLTTHIRTHTGEKPFACDICGRKFARSDERKRHTKIHLR
QKDKKADKSVVASSATSSLSSYPSPVATSYPSPVTTSYPSPATTSYPSPVPTSFSSPGSS
TYPSPVHSGFPSPSVATTYSSVPPAFPAQVSSFPSSAVTNSFSASTGLSDMTATFSPRTI
EIC
NT seq
1632 nt
NT seq
+upstream
nt +downstream
nt
atggccgcggccaaggccgagatgcagctgatgtccccgctgcagatctctgacccgttc
ggatcctttcctcactcgcccaccatggacaactaccctaagctggaggagatgatgctg
ctgagcaacggggctccccagttcctcggcgccgccggggccccagagggcagcggcagc
aacagcagcagcagcagcagcgggggcggtggaggcggcgggggcggcagcaacagcagc
agcagcagcagcaccttcaaccctcaggcggacacgggcgagcagccctacgagcacctg
accgcagagtcttttcctgacatctctctgaacaacgagaaggtgctggtggagaccagt
taccccagccaaaccactcgactgccccccatcacctatactggccgcttttccctggag
cctgcacccaacagtggcaacaccttgtggcccgagcccctcttcagcttggtcagtggc
ctagtgagcatgaccaacccaccggcctcctcgtcctcagcaccatctccagcggcctcc
tccgcctccgcctcccagagcccacccctgagctgcgcagtgccatccaacgacagcagt
cccatttactcagcggcacccaccttccccacgccgaacactgacattttccctgagcca
caaagccaggccttcccgggctcggcagggacagcgctccagtacccgcctcctgcctac
cctgccgccaagggtggcttccaggttcccatgatccccgactacctgtttccacagcag
cagggggatctgggcctgggcaccccagaccagaagcccttccagggcctggagagccgc
acccagcagccttcgctaacccctctgtctactattaaggcctttgccactcagtcgggc
tcccaggacctgaaggccctcaataccagctaccagtcccagctcatcaaacccagccgc
atgcgcaagtaccccaaccggcccagcaagacgcccccccacgaacgcccttacgcttgc
ccagtggagtcctgtgatcgccgcttctcccgctccgacgagctcacccgccacatccgc
atccacacaggccagaagcccttccagtgccgcatctgcatgcgcaacttcagccgcagc
gaccacctcaccacccacatccgcacccacacaggcgaaaagcccttcgcctgcgacatc
tgtggaagaaagtttgccaggagcgatgaacgcaagaggcataccaagatccacttgcgg
cagaaggacaagaaagcagacaaaagtgttgtggcctcttcggccacctcctctctctct
tcctacccgtccccggttgctacctcttacccgtccccggttactacctcttatccatcc
ccggccaccacctcatacccatcccctgtgcccacctccttctcctctcccggctcctcg
acctacccatcccctgtgcacagtggcttcccctccccgtcggtggccaccacgtactcc
tctgttccccctgctttcccggcccaggtcagcagcttcccttcctcagctgtcaccaac
tccttcagcgcctccacagggctttcggacatgacagcaaccttttctcccaggacaatt
gaaatttgctaa
Homo sapiens (human): 1959
Help
Entry
1959 CDS
T01001
Symbol
EGR2, AT591, CMT1D, CMT4E, KROX20
Name
(RefSeq) early growth response 2
KO
K12496
early growth response protein 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04625
C-type lectin receptor signaling pathway
hsa05161
Hepatitis B
hsa05166
Human T-cell leukemia virus 1 infection
hsa05203
Viral carcinogenesis
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
nt06162
Hepatitis B virus (HBV)
nt06263
Hepatocellular carcinoma
Element
N00509
HTLV-1 Tax to SRF-mediated transcription
N00532
HBV HBx to Egr-mediated transcription
Disease
H00264
Charcot-Marie-Tooth disease
H02357
Congenital hypomyelinating neuropathy
H02359
Dejerine-Sottas disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04625 C-type lectin receptor signaling pathway
1959 (EGR2)
09160 Human Diseases
09161 Cancer: overview
05203 Viral carcinogenesis
1959 (EGR2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
1959 (EGR2)
05161 Hepatitis B
1959 (EGR2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
1959 (EGR2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 SP/KLF family and related proteins
1959 (EGR2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF3446
zf-C2H2
zf-H2C2_2
zf-C2H2_4
zf-C2HC_2
zf-BED
zf-H2C2_5
Motif
Other DBs
NCBI-GeneID:
1959
NCBI-ProteinID:
NP_000390
OMIM:
129010
HGNC:
3239
Ensembl:
ENSG00000122877
UniProt:
P11161
LinkDB
All DBs
Position
10:complement(62811996..62819167)
Genome browser
AA seq
476 aa
AA seq
DB search
MMTAKAVDKIPVTLSGFVHQLSDNIYPVEDLAATSVTIFPNAELGGPFDQMNGVAGDGMI
NIDMTGEKRSLDLPYPSSFAPVSAPRNQTFTYMGKFSIDPQYPGASCYPEGIINIVSAGI
LQGVTSPASTTASSSVTSASPNPLATGPLGVCTMSQTQPDLDHLYSPPPPPPPYSGCAGD
LYQDPSAFLSAATTSTSSSLAYPPPPSYPSPKPATDPGLFPMIPDYPGFFPSQCQRDLHG
TAGPDRKPFPCPLDTLRVPPPLTPLSTIRNFTLGGPSAGVTGPGASGGSEGPRLPGSSSA
AAAAAAAAAYNPHHLPLRPILRPRKYPNRPSKTPVHERPYPCPAEGCDRRFSRSDELTRH
IRIHTGHKPFQCRICMRNFSRSDHLTTHIRTHTGEKPFACDYCGRKFARSDERKRHTKIH
LRQKERKSSAPSASVPAPSTASCSGGVQPGGTLCSSNSSSLGGGPLAPCSSRTRTP
NT seq
1431 nt
NT seq
+upstream
nt +downstream
nt
atgatgaccgccaaggccgtagacaaaatcccagtaactctcagtggttttgtgcaccag
ctgtctgacaacatctacccggtggaggacctcgccgccacgtcggtgaccatctttccc
aatgccgaactgggaggcccctttgaccagatgaacggagtggccggagatggcatgatc
aacattgacatgactggagagaagaggtcgttggatctcccatatcccagcagctttgct
cccgtctctgcacctagaaaccagaccttcacttacatgggcaagttctccattgaccct
cagtaccctggtgccagctgctacccagaaggcataatcaatattgtgagtgcaggcatc
ttgcaaggggtcacttccccagcttcaaccacagcctcatccagcgtcacctctgcctcc
cccaacccactggccacaggacccctgggtgtgtgcaccatgtcccagacccagcctgac
ctggaccacctgtactctccgccaccgcctcctcctccttattctggctgtgcaggagac
ctctaccaggacccttctgcgttcctgtcagcagccaccacctccacctcttcctctctg
gcctacccaccacctccttcctatccatcccccaagccagccacggacccaggtctcttc
ccaatgatcccagactatcctggattctttccatctcagtgccagagagacctacatggt
acagctggcccagaccgtaagccctttccctgcccactggacaccctgcgggtgccccct
ccactcactccactctctacaatccgtaactttaccctggggggccccagtgctggggtg
accggaccaggggccagtggaggcagcgagggaccccggctgcctggtagcagctcagca
gcagcagcagccgccgccgccgccgcctataacccacaccacctgccactgcggcccatt
ctgaggcctcgcaagtaccccaacagacccagcaagacgccggtgcacgagaggccctac
ccgtgcccagcagaaggctgcgaccggcggttctcccgctctgacgagctgacacggcac
atccgaatccacactgggcataagcccttccagtgtcggatctgcatgcgcaacttcagc
cgcagtgaccacctcaccacccatatccgcacccacaccggtgagaagcccttcgcctgt
gactactgtggccgaaagtttgcccggagtgatgagaggaagcgccacaccaagatccac
ctgagacagaaagagcggaaaagcagtgccccctctgcatcggtgccagccccctctaca
gcctcctgctctgggggcgtgcagcctgggggtaccctgtgcagcagtaacagcagcagt
cttggcggagggccgctcgccccttgctcctctcggacccggacaccttga
DBGET
integrated database retrieval system