Homo sapiens (human): 388112
Help
Entry
388112 CDS
T01001
Symbol
NANOGP8, NANOGP1, PN8
Name
(RefSeq) Nanog homeobox retrogene P8
KO
K10164
homeobox protein Nanog
Organism
hsa
Homo sapiens (human)
Pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa05205
Proteoglycans in cancer
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
388112 (NANOGP8)
09160 Human Diseases
09161 Cancer: overview
05205 Proteoglycans in cancer
388112 (NANOGP8)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
388112 (NANOGP8)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain ANTP: NKL
388112 (NANOGP8)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Homeodomain
Motif
Other DBs
NCBI-GeneID:
388112
NCBI-ProteinID:
NP_001342210
HGNC:
23106
Ensembl:
ENSG00000255192
LinkDB
All DBs
Position
15:complement(35083410..35085295)
Genome browser
AA seq
305 aa
AA seq
DB search
MSVDPACPQSLPCFEESDCKESSPMPVICGPEENYPSLQMSSAEMPHTETVSPLPSSMDL
LIQDSPDSSTSPKGKQPTSAENSVAKKEDKVPVKKQKTRTVFSSTQLCVLNDRFQRQKYL
SLQQMQELSNILNLSYKQVKTWFQNQRMKSKRWQKNNWPKNSNGVTQKASAPTYPSLYSS
YHQGCLVNPTGNLPMWSNQTWNNSTWSNQTQNIQSWSNHSWNTQTWCTQSWNNQAWNSPF
YNCGEESLQSCMHFQPNSPASDLEAALEAAGEGLNVIQQTTRYFSTPQTMDLFLNYSMNM
QPEDV
NT seq
918 nt
NT seq
+upstream
nt +downstream
nt
atgagtgtggatccagcttgtccccaaagcttgccttgctttgaagaatccgactgtaaa
gaatcttcacctatgcctgtgatttgtgggcctgaagaaaactatccatccttgcaaatg
tcttctgctgagatgcctcacacagagactgtctctcctcttccttcctccatggatctg
cttattcaggacagccctgattcttccaccagtcccaaaggcaaacaacccacttctgca
gagaatagtgtcgcaaaaaaggaagacaaggtcccggtcaagaaacagaagaccagaact
gtgttctcttccacccagctgtgtgtactcaatgatagatttcagagacagaaatacctc
agcctccagcagatgcaagaactctccaacatcctgaacctcagctacaaacaggtgaag
acctggttccagaaccagagaatgaaatctaagaggtggcagaaaaacaactggccgaag
aatagcaatggtgtgacgcagaaggcctcagcacctacctaccccagcctctactcttcc
taccaccagggatgcctggtgaacccgactgggaaccttccaatgtggagcaaccagacc
tggaacaattcaacctggagcaaccagacccagaacatccagtcctggagcaaccactcc
tggaacactcagacctggtgcacccaatcctggaacaatcaggcctggaacagtcccttc
tataactgtggagaggaatctctgcagtcctgcatgcacttccagccaaattctcctgcc
agtgacttggaggctgccttggaagctgctggggaaggccttaatgtaatacagcagacc
actaggtattttagtactccacaaaccatggatttattcctaaactactccatgaacatg
caacctgaagacgtgtga
Homo sapiens (human): 79923
Help
Entry
79923 CDS
T01001
Symbol
NANOG
Name
(RefSeq) Nanog homeobox
KO
K10164
homeobox protein Nanog
Organism
hsa
Homo sapiens (human)
Pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa05205
Proteoglycans in cancer
Drug target
Amcasertib:
D10903
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
79923 (NANOG)
09160 Human Diseases
09161 Cancer: overview
05205 Proteoglycans in cancer
79923 (NANOG)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
79923 (NANOG)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain ANTP: NKL
79923 (NANOG)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Homeodomain
Motif
Other DBs
NCBI-GeneID:
79923
NCBI-ProteinID:
NP_079141
OMIM:
607937
HGNC:
20857
Ensembl:
ENSG00000111704
Vega:
OTTHUMG00000166019
Pharos:
Q9H9S0
(Tbio)
UniProt:
Q9H9S0
A8K4D1
Structure
PDB
LinkDB
All DBs
Position
12:7789402..7799146
Genome browser
AA seq
305 aa
AA seq
DB search
MSVDPACPQSLPCFEASDCKESSPMPVICGPEENYPSLQMSSAEMPHTETVSPLPSSMDL
LIQDSPDSSTSPKGKQPTSAEKSVAKKEDKVPVKKQKTRTVFSSTQLCVLNDRFQRQKYL
SLQQMQELSNILNLSYKQVKTWFQNQRMKSKRWQKNNWPKNSNGVTQKASAPTYPSLYSS
YHQGCLVNPTGNLPMWSNQTWNNSTWSNQTQNIQSWSNHSWNTQTWCTQSWNNQAWNSPF
YNCGEESLQSCMQFQPNSPASDLEAALEAAGEGLNVIQQTTRYFSTPQTMDLFLNYSMNM
QPEDV
NT seq
918 nt
NT seq
+upstream
nt +downstream
nt
atgagtgtggatccagcttgtccccaaagcttgccttgctttgaagcatccgactgtaaa
gaatcttcacctatgcctgtgatttgtgggcctgaagaaaactatccatccttgcaaatg
tcttctgctgagatgcctcacacggagactgtctctcctcttccttcctccatggatctg
cttattcaggacagccctgattcttccaccagtcccaaaggcaaacaacccacttctgca
gagaagagtgtcgcaaaaaaggaagacaaggtcccggtcaagaaacagaagaccagaact
gtgttctcttccacccagctgtgtgtactcaatgatagatttcagagacagaaatacctc
agcctccagcagatgcaagaactctccaacatcctgaacctcagctacaaacaggtgaag
acctggttccagaaccagagaatgaaatctaagaggtggcagaaaaacaactggccgaag
aatagcaatggtgtgacgcagaaggcctcagcacctacctaccccagcctttactcttcc
taccaccagggatgcctggtgaacccgactgggaaccttccaatgtggagcaaccagacc
tggaacaattcaacctggagcaaccagacccagaacatccagtcctggagcaaccactcc
tggaacactcagacctggtgcacccaatcctggaacaatcaggcctggaacagtcccttc
tataactgtggagaggaatctctgcagtcctgcatgcagttccagccaaattctcctgcc
agtgacttggaggctgccttggaagctgctggggaaggccttaatgtaatacagcagacc
actaggtattttagtactccacaaaccatggatttattcctaaactactccatgaacatg
caacctgaagacgtgtga
DBGET
integrated database retrieval system
