Homo sapiens (human): 50943
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Entry
50943 CDS
T01001
Symbol
FOXP3, AIID, DIETER, IPEX, JM2, PIDX, XPID
Name
(RefSeq) forkhead box P3
KO
K10163
forkhead box P3
Organism
hsa
Homo sapiens (human)
Pathway
hsa04659
Th17 cell differentiation
hsa05321
Inflammatory bowel disease
Disease
H00107
Other well-defined immunodeficiency syndromes
H00512
Permanent neonatal diabetes mellitus
H01971
IPEX syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
50943 (FOXP3)
09160 Human Diseases
09163 Immune disease
05321 Inflammatory bowel disease
50943 (FOXP3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
50943 (FOXP3)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Fork head/winged helix other regulators
50943 (FOXP3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
FOXP-CC
Forkhead
Motif
Other DBs
NCBI-GeneID:
50943
NCBI-ProteinID:
NP_054728
OMIM:
300292
HGNC:
6106
Ensembl:
ENSG00000049768
Vega:
OTTHUMG00000024135
Pharos:
Q9BZS1
(Tbio)
UniProt:
Q9BZS1
Structure
PDB
LinkDB
All DBs
Position
X:complement(49250438..49264710)
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AA seq
431 aa
AA seq
DB search
MPNPRPGKPSAPSLALGPSPGASPSWRAAPKASDLLGARGPGGTFQGRDLRGGAHASSSS
LNPMPPSQLQLPTLPLVMVAPSGARLGPLPHLQALLQDRPHFMHQLSTVDAHARTPVLQV
HPLESPAMISLTPPTTATGVFSLKARPGLPPGINVASLEWVSREPALLCTFPNPSAPRKD
STLSAVPQSSYPLLANGVCKWPGCEKVFEEPEDFLKHCQADHLLDEKGRAQCLLQREMVQ
SLEQQLVLEKEKLSAMQAHLAGKMALTKASSVASSDKGSCCIVAAGSQGPVVPAWSGPRE
APDSLFAVRRHLWGSHGNSTFPEFLHNMDYFKFHNMRPPFTYATLIRWAILEAPEKQRTL
NEIYHWFTRMFAFFRNHPATWKNAIRHNLSLHKCFVRVESEKGAVWTVDELEFRKKRSQR
PSRCSNPTPGP
NT seq
1296 nt
NT seq
+upstream
nt +downstream
nt
atgcccaaccccaggcctggcaagccctcggccccttccttggcccttggcccatcccca
ggagcctcgcccagctggagggctgcacccaaagcctcagacctgctgggggcccggggc
ccagggggaaccttccagggccgagatcttcgaggcggggcccatgcctcctcttcttcc
ttgaaccccatgccaccatcgcagctgcagctgcccacactgcccctagtcatggtggca
ccctccggggcacggctgggccccttgccccacttacaggcactcctccaggacaggcca
catttcatgcaccagctctcaacggtggatgcccacgcccggacccctgtgctgcaggtg
caccccctggagagcccagccatgatcagcctcacaccacccaccaccgccactggggtc
ttctccctcaaggcccggcctggcctcccacctgggatcaacgtggccagcctggaatgg
gtgtccagggagccggcactgctctgcaccttcccaaatcccagtgcacccaggaaggac
agcaccctttcggctgtgccccagagctcctacccactgctggcaaatggtgtctgcaag
tggcccggatgtgagaaggtcttcgaagagccagaggacttcctcaagcactgccaggcg
gaccatcttctggatgagaagggcagggcacaatgtctcctccagagagagatggtacag
tctctggagcagcagctggtgctggagaaggagaagctgagtgccatgcaggcccacctg
gctgggaaaatggcactgaccaaggcttcatctgtggcatcatccgacaagggctcctgc
tgcatcgtagctgctggcagccaaggccctgtcgtcccagcctggtctggcccccgggag
gcccctgacagcctgtttgctgtccggaggcacctgtggggtagccatggaaacagcaca
ttcccagagttcctccacaacatggactacttcaagttccacaacatgcgaccccctttc
acctacgccacgctcatccgctgggccatcctggaggctccagagaagcagcggacactc
aatgagatctaccactggttcacacgcatgtttgccttcttcagaaaccatcctgccacc
tggaagaacgccatccgccacaacctgagtctgcacaagtgctttgtgcgggtggagagc
gagaagggggctgtgtggaccgtggatgagctggagttccgcaagaaacggagccagagg
cccagcaggtgttccaaccctacacctggcccctga
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