KEGG   Homo sapiens (human): 2299
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)
SSDB
Motif
Pfam: Forkhead
Other DBs
NCBI-GeneID: 2299
NCBI-ProteinID: NP_036320
OMIM: 601093
HGNC: 3815
Ensembl: ENSG00000168269
UniProt: Q12951 E0XEN6
Position
5:170105897..170109737
AA seq 378 aa
MSSFDLPAPSPPRCSPQFPSIGQEPPEMNLYYENFFHPQGVPSPQRPSFEGGGEYGATPN
PYLWFNGPTMTPPPYLPGPNASPFLPQAYGVQRPLLPSVSGLGGSDLGWLPIPSQEELMK
LVRPPYSYSALIAMAIHGAPDKRLTLSQIYQYVADNFPFYNKSKAGWQNSIRHNLSLNDC
FKKVPRDEDDPGKGNYWTLDPNCEKMFDNGNFRRKRKRKSDVSSSTASLALEKTESSLPV
DSPKTTEPQDILDGASPGGTTSSPEKRPSPPPSGAPCLNSFLSSMTAYVSGGSPTSHPLV
TPGLSPEPSDKTGQNSLTFNSFSPLTNLSNHSGGGDWANPMPTNMLSYGGSVLSQFSPHF
YNSVNTSGVLYPREGTEV
NT seq 1137 nt   +upstreamnt  +downstreamnt
atgagctccttcgacctgccggcgccctccccacctcgctgcagcccccagttccccagc
atcggccaggagccccccgagatgaacctctactatgagaacttcttccacccacagggc
gtgcccagccctcagcggccctccttcgaggggggcggcgagtatggggccacccccaac
ccctacctctggttcaacgggcccaccatgaccccgccaccctacctgcccggccccaac
gccagccccttcctgccccaggcctatggagtgcagaggccgctgctgcccagcgtgtcg
gggcttggggggagcgacctgggctggctgcccatcccctcgcaggaggagctgatgaag
ctggtgcggccaccctattcctactcggctctcatcgccatggccatccacggggcaccc
gacaagcgcctcactctcagccagatctaccagtacgtggccgacaacttccccttctac
aacaagagcaaggccggctggcagaactccatccgccacaacctgtcgctcaacgactgc
ttcaagaaggtgccccgcgacgaggacgacccgggcaaagggaattactggaccctggac
cccaactgtgagaaaatgttcgacaatggaaatttccgcaggaaaaggaagagaaaatca
gatgtttcctctagcacagcctccttggccttagagaagacagagagcagtctcccggtg
gacagccccaagaccacggagcctcaggacatcttggatggagcctcaccagggggcacc
accagctccccagagaagcggccctcccctcccccatcaggcgccccttgccttaacagc
ttcctttcctctatgacagcctatgtgagcggggggagccccacgagccaccccttggtc
acaccaggactgagccctgagcccagtgacaagacggggcagaactcactgaccttcaac
tccttctccccgctcaccaacctcagcaaccacagcggtgggggtgactgggcgaacccc
atgcccaccaacatgctcagctatggaggatctgtgctcagccaattcagccctcacttc
tacaacagtgtcaacaccagtggtgtcctctaccccagggagggcaccgaggtctag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (5)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (12)   
   RefSeq(nuc) (4)   
   GenBank (4)   
   EMBL (4)   
Protein domain (1)   
   Pfam (1)   
All databases (39)   

Download RDF
DBGET integrated database retrieval system