KEGG   Homo sapiens (human): 1959
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)
SSDB
Motif
Pfam: DUF3446 zf-C2H2 zf-H2C2_2 zf-C2H2_4 zf-C2HC_2 zf-BED zf-H2C2_5
Other DBs
NCBI-GeneID: 1959
NCBI-ProteinID: NP_000390
OMIM: 129010
HGNC: 3239
Ensembl: ENSG00000122877
UniProt: P11161
Position
10:complement(62811996..62819167)
AA seq 476 aa
MMTAKAVDKIPVTLSGFVHQLSDNIYPVEDLAATSVTIFPNAELGGPFDQMNGVAGDGMI
NIDMTGEKRSLDLPYPSSFAPVSAPRNQTFTYMGKFSIDPQYPGASCYPEGIINIVSAGI
LQGVTSPASTTASSSVTSASPNPLATGPLGVCTMSQTQPDLDHLYSPPPPPPPYSGCAGD
LYQDPSAFLSAATTSTSSSLAYPPPPSYPSPKPATDPGLFPMIPDYPGFFPSQCQRDLHG
TAGPDRKPFPCPLDTLRVPPPLTPLSTIRNFTLGGPSAGVTGPGASGGSEGPRLPGSSSA
AAAAAAAAAYNPHHLPLRPILRPRKYPNRPSKTPVHERPYPCPAEGCDRRFSRSDELTRH
IRIHTGHKPFQCRICMRNFSRSDHLTTHIRTHTGEKPFACDYCGRKFARSDERKRHTKIH
LRQKERKSSAPSASVPAPSTASCSGGVQPGGTLCSSNSSSLGGGPLAPCSSRTRTP
NT seq 1431 nt   +upstreamnt  +downstreamnt
atgatgaccgccaaggccgtagacaaaatcccagtaactctcagtggttttgtgcaccag
ctgtctgacaacatctacccggtggaggacctcgccgccacgtcggtgaccatctttccc
aatgccgaactgggaggcccctttgaccagatgaacggagtggccggagatggcatgatc
aacattgacatgactggagagaagaggtcgttggatctcccatatcccagcagctttgct
cccgtctctgcacctagaaaccagaccttcacttacatgggcaagttctccattgaccct
cagtaccctggtgccagctgctacccagaaggcataatcaatattgtgagtgcaggcatc
ttgcaaggggtcacttccccagcttcaaccacagcctcatccagcgtcacctctgcctcc
cccaacccactggccacaggacccctgggtgtgtgcaccatgtcccagacccagcctgac
ctggaccacctgtactctccgccaccgcctcctcctccttattctggctgtgcaggagac
ctctaccaggacccttctgcgttcctgtcagcagccaccacctccacctcttcctctctg
gcctacccaccacctccttcctatccatcccccaagccagccacggacccaggtctcttc
ccaatgatcccagactatcctggattctttccatctcagtgccagagagacctacatggt
acagctggcccagaccgtaagccctttccctgcccactggacaccctgcgggtgccccct
ccactcactccactctctacaatccgtaactttaccctggggggccccagtgctggggtg
accggaccaggggccagtggaggcagcgagggaccccggctgcctggtagcagctcagca
gcagcagcagccgccgccgccgccgcctataacccacaccacctgccactgcggcccatt
ctgaggcctcgcaagtaccccaacagacccagcaagacgccggtgcacgagaggccctac
ccgtgcccagcagaaggctgcgaccggcggttctcccgctctgacgagctgacacggcac
atccgaatccacactgggcataagcccttccagtgtcggatctgcatgcgcaacttcagc
cgcagtgaccacctcaccacccatatccgcacccacaccggtgagaagcccttcgcctgt
gactactgtggccgaaagtttgcccggagtgatgagaggaagcgccacaccaagatccac
ctgagacagaaagagcggaaaagcagtgccccctctgcatcggtgccagccccctctaca
gcctcctgctctgggggcgtgcagcctgggggtaccctgtgcagcagtaacagcagcagt
cttggcggagggccgctcgccccttgctcctctcggacccggacaccttga

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