Homo sapiens (human): 2299
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Entry
2299 CDS
T01001
Symbol
FOXI1, FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, HFH3
Name
(RefSeq) forkhead box I1
KO
K09401
forkhead box protein I
Organism
hsa
Homo sapiens (human)
Disease
H00251
Thyroid dyshormonogenesis
H00605
Deafness, autosomal recessive
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
2299 (FOXI1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Fork head/winged helix other regulators
2299 (FOXI1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Forkhead
Motif
Other DBs
NCBI-GeneID:
2299
NCBI-ProteinID:
NP_036320
OMIM:
601093
HGNC:
3815
Ensembl:
ENSG00000168269
UniProt:
Q12951
E0XEN6
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All DBs
Position
5:170105897..170109737
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AA seq
378 aa
AA seq
DB search
MSSFDLPAPSPPRCSPQFPSIGQEPPEMNLYYENFFHPQGVPSPQRPSFEGGGEYGATPN
PYLWFNGPTMTPPPYLPGPNASPFLPQAYGVQRPLLPSVSGLGGSDLGWLPIPSQEELMK
LVRPPYSYSALIAMAIHGAPDKRLTLSQIYQYVADNFPFYNKSKAGWQNSIRHNLSLNDC
FKKVPRDEDDPGKGNYWTLDPNCEKMFDNGNFRRKRKRKSDVSSSTASLALEKTESSLPV
DSPKTTEPQDILDGASPGGTTSSPEKRPSPPPSGAPCLNSFLSSMTAYVSGGSPTSHPLV
TPGLSPEPSDKTGQNSLTFNSFSPLTNLSNHSGGGDWANPMPTNMLSYGGSVLSQFSPHF
YNSVNTSGVLYPREGTEV
NT seq
1137 nt
NT seq
+upstream
nt +downstream
nt
atgagctccttcgacctgccggcgccctccccacctcgctgcagcccccagttccccagc
atcggccaggagccccccgagatgaacctctactatgagaacttcttccacccacagggc
gtgcccagccctcagcggccctccttcgaggggggcggcgagtatggggccacccccaac
ccctacctctggttcaacgggcccaccatgaccccgccaccctacctgcccggccccaac
gccagccccttcctgccccaggcctatggagtgcagaggccgctgctgcccagcgtgtcg
gggcttggggggagcgacctgggctggctgcccatcccctcgcaggaggagctgatgaag
ctggtgcggccaccctattcctactcggctctcatcgccatggccatccacggggcaccc
gacaagcgcctcactctcagccagatctaccagtacgtggccgacaacttccccttctac
aacaagagcaaggccggctggcagaactccatccgccacaacctgtcgctcaacgactgc
ttcaagaaggtgccccgcgacgaggacgacccgggcaaagggaattactggaccctggac
cccaactgtgagaaaatgttcgacaatggaaatttccgcaggaaaaggaagagaaaatca
gatgtttcctctagcacagcctccttggccttagagaagacagagagcagtctcccggtg
gacagccccaagaccacggagcctcaggacatcttggatggagcctcaccagggggcacc
accagctccccagagaagcggccctcccctcccccatcaggcgccccttgccttaacagc
ttcctttcctctatgacagcctatgtgagcggggggagccccacgagccaccccttggtc
acaccaggactgagccctgagcccagtgacaagacggggcagaactcactgaccttcaac
tccttctccccgctcaccaacctcagcaaccacagcggtgggggtgactgggcgaacccc
atgcccaccaacatgctcagctatggaggatctgtgctcagccaattcagccctcacttc
tacaacagtgtcaacaccagtggtgtcctctaccccagggagggcaccgaggtctag
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