Homo sapiens (human): 7490
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Entry
7490 CDS
T01001
Symbol
WT1, AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1, WT33
Name
(RefSeq) WT1 transcription factor
KO
K09234
Wilms tumor protein 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa05202
Transcriptional misregulation in cancer
Network
nt06240
Transcription (cancer)
Element
N00137
EWSR1-WT1 fusion to transcriptional activation
Disease
H00607
46,XY gonadal dysgenesis
H01657
Nephrotic syndrome
H01985
Desmoplastic small round cell tumor
H02301
Nephroblastoma
Drug target
Adegramotide acetate:
D11058
Adegrapepimut-S:
D11057
Elatipepimut-S:
D11059
Nelatimotide trifluoroacetate:
D11060
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
7490 (WT1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
7490 (WT1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 SP/KLF family and related proteins
7490 (WT1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
WT1
zf-H2C2_2
zf-C2H2
zf-C2H2_4
FOXP-CC
zf-C2H2_8
zf-met
DUF7565
Zap1_zf1
Motif
Other DBs
NCBI-GeneID:
7490
NCBI-ProteinID:
NP_001415960
OMIM:
607102
HGNC:
12796
Ensembl:
ENSG00000184937
UniProt:
P19544
A0A481V744
Structure
PDB
PDBj
LinkDB
All DBs
Position
11:complement(32387775..32435539)
Genome browser
AA seq
449 aa
AA seq
DB search
MGSDVRDLNALLPAVPSLGGGGGCALPVSGAAQWAPVLDFAPPGASAYGSLGGPAPPPAP
PPPPPPPPHSFIKQEPSWGGAEPHEEQCLSAFTVHFSGQFTGTAGACRYGPFGPPPPSQA
SSGQARMFPNAPYLPSCLESQPAIRNQGYSTVTFDGTPSYGHTPSHHAAQFPNHSFKHED
PMGQQGSLGEQQYSVPPPVYGCHTPTDSCTGSQALLLRTPYSSDNLYQMTSQLECMTWNQ
MNLGATLKGVAAGSSSSVKWTEGQSNHSTGYESDNHTTPILCGAQYRIHTHGVFRGIQDV
RRVPGVAPTLVRSASETSEKRPFMCAYPGCNKRYFKLSHLQMHSRKHTGEKPYQCDFKDC
ERRFSRSDQLKRHQRRHTGVKPFQCKTCQRKFSRSDHLKTHTRTHTGKTSEKPFSCRWPS
CQKKFARSDELVRHHNMHQRNMTKLQLAL
NT seq
1350 nt
NT seq
+upstream
nt +downstream
nt
atgggctccgacgtgcgggacctgaacgcgctgctgcccgccgtcccctccctgggtggc
ggcggcggctgtgccctgcctgtgagcggcgcggcgcagtgggcgccggtgctggacttt
gcgcccccgggcgcttcggcttacgggtcgttgggcggccccgcgccgccaccggctccg
ccgccacccccgccgccgccgcctcactccttcatcaaacaggagccgagctggggcggc
gcggagccgcacgaggagcagtgcctgagcgccttcactgtccacttttccggccagttc
actggcacagccggagcctgtcgctacgggcccttcggtcctcctccgcccagccaggcg
tcatccggccaggccaggatgtttcctaacgcgccctacctgcccagctgcctcgagagc
cagcccgctattcgcaatcagggttacagcacggtcaccttcgacgggacgcccagctac
ggtcacacgccctcgcaccatgcggcgcagttccccaaccactcattcaagcatgaggat
cccatgggccagcagggctcgctgggtgagcagcagtactcggtgccgcccccggtctat
ggctgccacacccccaccgacagctgcaccggcagccaggctttgctgctgaggacgccc
tacagcagtgacaatttataccaaatgacatcccagcttgaatgcatgacctggaatcag
atgaacttaggagccaccttaaagggagttgctgctgggagctccagctcagtgaaatgg
acagaagggcagagcaaccacagcacagggtacgagagcgataaccacacaacgcccatc
ctctgcggagcccaatacagaatacacacgcacggtgtcttcagaggcattcaggatgtg
cgacgtgtgcctggagtagccccgactcttgtacggtcggcatctgagaccagtgagaaa
cgccccttcatgtgtgcttacccaggctgcaataagagatattttaagctgtcccactta
cagatgcacagcaggaagcacactggtgagaaaccataccagtgtgacttcaaggactgt
gaacgaaggttttctcgttcagaccagctcaaaagacaccaaaggagacatacaggtgtg
aaaccattccagtgtaaaacttgtcagcgaaagttctcccggtccgaccacctgaagacc
cacaccaggactcatacaggtaaaacaagtgaaaagcccttcagctgtcggtggccaagt
tgtcagaaaaagtttgcccggtcagatgaattagtccgccatcacaacatgcatcagaga
aacatgaccaaactccagctggcgctttga
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