Neogale vison (American mink): 122900713
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Entry
122900713 CDS
T08764
Symbol
EGR2
Name
(RefSeq) E3 SUMO-protein ligase EGR2 isoform X1
KO
K12496
early growth response protein 2
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04625
C-type lectin receptor signaling pathway
nvs05161
Hepatitis B
nvs05166
Human T-cell leukemia virus 1 infection
nvs05203
Viral carcinogenesis
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09150 Organismal Systems
09151 Immune system
04625 C-type lectin receptor signaling pathway
122900713 (EGR2)
09160 Human Diseases
09161 Cancer: overview
05203 Viral carcinogenesis
122900713 (EGR2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
122900713 (EGR2)
05161 Hepatitis B
122900713 (EGR2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
nvs03000
]
122900713 (EGR2)
Transcription factors [BR:
nvs03000
]
Eukaryotic type
Zinc finger
Cys2His2 SP/KLF family and related proteins
122900713 (EGR2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF3446
zf-C2H2
zf-H2C2_2
zf-C2H2_4
zf-C2HC_2
zf-C2H2_STOP2_C
zf-BED
zf-C2H2_15
C2CH-3rd_BIRD-IDD
zf-C2H2_ZNF462_1st
DUF7565
zf-H2C2_5
Motif
Other DBs
NCBI-GeneID:
122900713
NCBI-ProteinID:
XP_044095542
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All DBs
Position
2:complement(177667790..177674382)
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AA seq
422 aa
AA seq
DB search
MNGVAGDGMINIDMTGEKRSLDLPYPSSFAPVSAPRNQTFTYMGKFSIDPQYPGASCYPE
GIINIVSAGILQGVTSPASTTASSSVTSASPNPLATGPLGVCTMSQTQPDLDQLYSPPPP
PPYSGCAGDIYQDPSAFLSAATTSSSSSLAYPPPPSYPSPKPATDPGLFPMIPDYPGFFQ
PQCPRDLHGTAGPDRKPFPCPLDSLRVPPPLTPLSTIRNFTLGGPSSGATGPGASGGSEG
PRLPGSSSAAAAAAAYNPHHLPLRPILRPRKYPNRPSKTPVHERPYPCPAEGCDRRFSRS
DELTRHIRIHTGHKPFQCRICMRNFSRSDHLTTHIRTHTGEKPFACDYCGRKFARSDERK
RHTKIHLRQKERKSSAPSSAVPAASTASCPGSAQAGGPLCGSTSGTLGGGSLAPCSSRTR
TP
NT seq
1269 nt
NT seq
+upstream
nt +downstream
nt
atgaacggagtagccggagatggcatgatcaacattgacatgaccggagagaagaggtcc
ttggatctcccatatcccagcagctttgctcccgtctctgcacctagaaaccagaccttc
acgtacatgggcaagttctccattgacccccagtaccctggtgccagctgctacccagaa
ggcatcatcaatattgtgagtgcaggcatcctgcaaggggttacctcccctgcttcgacc
acagcctcgtccagcgtcacgtctgcttcccccaacccactggccacaggacccctgggt
gtgtgcaccatgtctcagacccagcctgacctggaccaactgtactctccaccgccacct
cctccttattctggctgtgcaggagacatctaccaggacccctcggcattcctgtcagca
gccaccacctccagctcctcctctctggcctacccaccacctccttcctacccctcccct
aagccagccacggaccccggtctctttcccatgatcccagactatcctggattcttccaa
ccacagtgtccaagagacctacatggtacagctggcccagaccgcaaaccctttccctgc
cctctggactccttgcgagtccctcctccactcactccactctccaccattcgcaacttt
accctggggggccccagttctggggccacagggccaggggccagtggaggcagtgaggga
ccccggctgcctggcagcagctcagccgccgctgcggccgccgcttataacccgcaccac
ctgccgctgcggcccattctgaggcctcgcaagtaccccaacaggcctagcaagacccca
gtgcacgagaggccctacccgtgcccagcagaaggctgtgaccgccgcttctcccgctct
gacgagctgacccgacacatccgaatccacacgggacacaagcccttccagtgtcggatt
tgcatgcgcaacttcagccgcagcgaccacctcactacccacatccgcacccacacgggc
gagaagcctttcgcctgtgactactgcggccgcaagtttgcccggagtgacgagaggaag
cgtcacaccaagatccacctgagacagaaggagcgcaaaagcagtgccccctcctcagcc
gtgccagctgcgtccacggcctcgtgccccgggagtgcacaggctggggggcccctgtgc
ggcagcaccagcggcacgctgggtggaggatctctggccccttgctcctctcggacccga
acaccttga
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