Homo sapiens (human): 27022
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Entry
27022 CDS
T01001
Symbol
FOXD3, AIS1, Genesis, HFH2, VAMAS2
Name
(RefSeq) forkhead box D3
KO
K09397
forkhead box protein D
Organism
hsa
Homo sapiens (human)
Disease
H01372
Vitiligo
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
27022 (FOXD3)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Fork head/winged helix other regulators
27022 (FOXD3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Forkhead
Motif
Other DBs
NCBI-GeneID:
27022
NCBI-ProteinID:
NP_036315
OMIM:
611539
HGNC:
3804
Ensembl:
ENSG00000187140
UniProt:
Q9UJU5
LinkDB
All DBs
Position
1:63322567..63325128
Genome browser
AA seq
478 aa
AA seq
DB search
MTLSGGGSASDMSGQTVLTAEDVDIDVVGEGDDGLEEKDSDAGCDSPAGPPELRLDEADE
VPPAAPHHGQPQPPHQQPLTLPKEAAGAGAGPGGDVGAPEADGCKGGVGGEEGGASGGGP
GAGSGSAGGLAPSKPKNSLVKPPYSYIALITMAILQSPQKKLTLSGICEFISNRFPYYRE
KFPAWQNSIRHNLSLNDCFVKIPREPGNPGKGNYWTLDPQSEDMFDNGSFLRRRKRFKRH
QQEHLREQTALMMQSFGAYSLAAAAGAAGPYGRPYGLHPAAAAGAYSHPAAAAAAAAAAA
LQYPYALPPVAPVLPPAVPLLPSGELGRKAAAFGSQLGPGLQLQLNSLGAAAAAAGTAGA
AGTTASLIKSEPSARPSFSIENIIGGGPAAPGGSAVGAGVAGGTGGSGGGSTAQSFLRPP
GTVQSAALMATHQPLSLSRTTATIAPILSVPLSGQFLQPAASAAAAAAAAAQAKWPAQ
NT seq
1437 nt
NT seq
+upstream
nt +downstream
nt
atgaccctctccggcggcggcagcgccagcgacatgtccggccagacggtgctgacggcc
gaggacgtggacatcgatgtggtgggcgagggcgacgacgggctggaagagaaggacagc
gacgcaggttgcgatagccccgcggggccgccggagctgcgcctggacgaggcggacgag
gtgcccccggcggcaccccatcacggacagcctcagccgccccaccagcagcccctgaca
ttgcccaaggaggcggccggagccggggccggaccggggggcgacgtgggcgcgccggag
gcggacggctgcaagggcggtgttggcggcgaggagggcggcgcgagcggcggcgggcct
ggcgcgggcagcggttcggcgggaggcctggccccgagcaagcccaagaacagcctagtg
aagccgccttactcgtacatcgcgctcatcaccatggccatcctgcagagcccgcagaag
aagctgaccctgagcggcatctgcgagttcatcagcaaccgcttcccctactacagggag
aagttccccgcctggcagaacagcatccgccacaacctctcactcaacgactgcttcgtc
aagatcccccgcgagccgggcaacccgggcaagggcaactactggaccctggacccgcag
tccgaggacatgttcgacaacggcagcttcctgcggcgccggaaacgcttcaagcgccac
cagcaggagcacctgcgcgagcagacggcgctcatgatgcagagcttcggcgcttacagc
ctggcggcggcggccggcgccgcgggaccctacggccgcccctacggcctgcaccctgcg
gcggcggccggtgcctattcgcacccggcagcggcggcggccgcggctgctgcggcggcg
ctccagtacccgtacgcgctgccgccggtggcaccggtgctgcctcccgctgtgccgctg
ctgccctcgggcgagctgggccgcaaagcggccgccttcggctcacagctcggcccgggc
ctgcagctgcagctcaatagcctgggcgccgccgcggccgctgcgggcacagcgggcgcc
gcgggcaccaccgcgtcgctcatcaagtccgagccaagcgcgcggccgtcgttcagcatc
gagaacatcataggtgggggccccgcggctcctgggggctcggcggtgggcgctggggtc
gccggcggcactgggggttcagggggcggcagcacggcgcagtcgtttctgcggccaccc
gggaccgtgcagtcggcagcgctcatggccacccaccaaccgctgtcgctgagccggacg
actgccaccatcgcgcccattcttagcgtgccactctccggacagtttctgcagcccgca
gcctcggccgccgccgctgctgcggccgccgctcaagccaaatggccggcgcaatag
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