Homo sapiens (human): 2002
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Entry
2002 CDS
T01001
Symbol
ELK1
Name
(RefSeq) ETS transcription factor ELK1
KO
K04375
ETS domain-containing protein Elk-1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04010
MAPK signaling pathway
hsa04012
ErbB signaling pathway
hsa04014
Ras signaling pathway
hsa04510
Focal adhesion
hsa04910
Insulin signaling pathway
hsa04912
GnRH signaling pathway
hsa04921
Oxytocin signaling pathway
hsa05140
Leishmaniasis
hsa05161
Hepatitis B
hsa05163
Human cytomegalovirus infection
hsa05166
Human T-cell leukemia virus 1 infection
hsa05200
Pathways in cancer
hsa05205
Proteoglycans in cancer
hsa05213
Endometrial cancer
hsa05225
Hepatocellular carcinoma
Network
nt06162
Hepatitis B virus (HBV)
nt06220
Calcium signaling (cancer)
nt06263
Hepatocellular carcinoma
nt06323
KISS1-GnRH-LH/FSH-E2 signaling
Element
N00227
TGFA-EGFR-PLCG-PKC signaling pathway
N00228
TGFA-overexpression to PLCG-PKC signaling pathway
N00540
HBV HBx to RAS-ERK signaling pathway
N00873
GnRH-GnRHR-PLCB-PKC signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04014 Ras signaling pathway
2002 (ELK1)
09150 Organismal Systems
09152 Endocrine system
04921 Oxytocin signaling pathway
2002 (ELK1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
2002 (ELK1)
05205 Proteoglycans in cancer
2002 (ELK1)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
2002 (ELK1)
05213 Endometrial cancer
2002 (ELK1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
2002 (ELK1)
05161 Hepatitis B
2002 (ELK1)
05163 Human cytomegalovirus infection
2002 (ELK1)
09174 Infectious disease: parasitic
05140 Leishmaniasis
2002 (ELK1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
2002 (ELK1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Tryptophan clusters Ets-type
2002 (ELK1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ets
Motif
Other DBs
NCBI-GeneID:
2002
NCBI-ProteinID:
NP_001107595
OMIM:
311040
HGNC:
3321
Ensembl:
ENSG00000126767
UniProt:
P19419
Structure
PDB
PDBj
LinkDB
All DBs
Position
X:complement(47635520..47650604)
Genome browser
AA seq
428 aa
AA seq
DB search
MDPSVTLWQFLLQLLREQGNGHIISWTSRDGGEFKLVDAEEVARLWGLRKNKTNMNYDKL
SRALRYYYDKNIIRKVSGQKFVYKFVSYPEVAGCSTEDCPPQPEVSVTSTMPNVAPAAIH
AAPGDTVSGKPGTPKGAGMAGPGGLARSSRNEYMRSGLYSTFTIQSLQPQPPPHPRPAVV
LPSAAPAGAAAPPSGSRSTSPSPLEACLEAEEAGLPLQVILTPPEAPNLKSEELNVEPGL
GRALPPEVKVEGPKEELEVAGERGFVPETTKAEPEVPPQEGVPARLPAVVMDTAGQAGGH
AASSPEISQPQKGRKPRDLELPLSPSLLGGPGPERTPGSGSGSGLQAPGPALTPSLLPTH
TLTPVLLTPSSLPPSIHFWSTLSPIAPRSPAKLSFQFPSSGSAQVHIPSISVDGLSTPVV
LSPGPQKP
NT seq
1287 nt
NT seq
+upstream
nt +downstream
nt
atggacccatctgtgacgctgtggcagtttctgctgcagctgctgagagagcaaggcaat
ggccacatcatctcctggacttcacgggatggtggtgaattcaagctggtggatgcagag
gaggtggcccggctgtgggggctacgcaagaacaagaccaacatgaattacgacaagctc
agccgggccttgcggtactactatgacaagaacatcatccgcaaggtgagcggccagaag
ttcgtctacaagtttgtgtcctaccctgaggtcgcagggtgctccactgaggactgcccg
ccccagccagaggtgtctgttacctccaccatgccaaatgtggcccctgctgctatacat
gccgccccaggggacactgtctctggaaagccaggcacacccaagggtgcaggaatggca
ggcccaggcggtttggcacgcagcagccggaacgagtacatgcgctcgggcctctattcc
accttcaccatccagtctctgcagccgcagccaccccctcatcctcggcctgctgtggtg
ctccccagtgcagctcctgcaggggcagcagcgcccccctcggggagcaggagcaccagt
ccaagccccttggaggcctgtctggaggctgaagaggccggcttgcctctgcaggtcatc
ctgaccccgcccgaggccccaaacctgaaatcggaagagcttaatgtggagccgggtttg
ggccgggctttgcccccagaagtgaaagtagaagggcccaaggaagagttggaagttgcg
ggggagagagggtttgtgccagaaaccaccaaggccgagccagaagtccctccacaggag
ggcgtgccagcccggctgcccgcggttgttatggacaccgcagggcaggcgggcggccat
gcggcttccagccctgagatctcccagccgcagaagggccggaagccccgggacctagag
cttccactcagcccgagcctgctaggtgggccgggacccgaacggaccccaggatcggga
agtggctccggcctccaggctccggggccggcgctgaccccatccctgcttcctacgcat
acattgaccccggtgctgctgacacccagctcgctgcctcctagcattcacttctggagc
accctgagtcccattgcgccccgtagcccggccaagctctccttccagtttccatccagt
ggcagcgcccaggtgcacatcccttctatcagcgtggatggcctctcgacccccgtggtg
ctctccccagggccccagaagccatga
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