KEGG   Homo sapiens (human): 8456
Entry
8456              CDS       T01001                                 
Symbol
FOXN1, FKHL20, RONU, TIDAND, TLIND, WHN
Name
(RefSeq) forkhead box N1
  KO
K09407  forkhead box protein N
Organism
hsa  Homo sapiens (human)
Disease
H01181  T-cell immunodeficiency congenital alopecia and nail dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    8456 (FOXN1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Fork head/winged helix developmental regulators
    8456 (FOXN1)
SSDB
Motif
Pfam: Forkhead
Other DBs
NCBI-GeneID: 8456
NCBI-ProteinID: NP_003584
OMIM: 600838
HGNC: 12765
Ensembl: ENSG00000109101
UniProt: O15353
Structure
Position
17:28506348..28538900
AA seq 648 aa
MVSLPPPQSDVTLPGPTRLEGERQGDLMQAPGLPGSPAPQSKHAGFSCSSFVSDGPPERT
PSLPPHSPRIASPGPEQVQGHCPAGPGPGPFRLSPSDKYPGFGFEEAAASSPGRFLKGSH
APFHPYKRPFHEDVFPEAETTLALKGHSFKTPGPLEAFEEIPVDVAEAEAFLPGFSAEAW
CNGLPYPSQEHGPQVLGSEVKVKPPVLESGAGMFCYQPPLQHMYCSSQPPFHQYSPGGGS
YPIPYLGSSHYQYQRMAPQASTDGHQPLFPKPIYSYSILIFMALKNSKTGSLPVSEIYNF
MTEHFPYFKTAPDGWKNSVRHNLSLNKCFEKVENKSGSSSRKGCLWALNPAKIDKMQEEL
QKWKRKDPIAVRKSMAKPEELDSLIGDKREKLGSPLLGCPPPGLSGSGPIRPLAPPAGLS
PPLHSLHPAPGPIPGKNPLQDLLMGHTPSCYGQTYLHLSPGLAPPGPPQPLFPQPDGHLE
LRAQPGTPQDSPLPAHTPPSHSAKLLAEPSPARTMHDTLLPDGDLGTDLDAINPSLTDFD
FQGNLWEQLKDDSLALDPLVLVTSSPTSSSMPPPQPPPHCFPPGPCLTETGSGAGDLAAP
GSGGSGALGDLHLTTLYSAFMELEPTPPTAPAGPSVYLSPSSKPVALA
NT seq 1947 nt   +upstreamnt  +downstreamnt
atggtgtcgctacccccgccgcagtctgacgtcacgctgccgggccccaccagactggag
ggcgagcgccaaggggacctcatgcaggcaccgggcctcccaggctcccctgccccacag
agtaagcatgccggcttcagctgctcgtcatttgtgtccgacggccctccagagaggaca
ccctcactgcccccacacagcccccgcattgcgtcaccagggcccgagcaagtccagggc
cactgcccagccggccccggccctgggcccttcaggctctcaccctcagacaagtatcct
ggctttggctttgaggaggccgcagcaagcagccctgggcgattcctcaagggcagccac
gcgcccttccacccgtacaagcggcctttccatgaggacgtcttcccagaggccgagacc
accctggccctcaaaggacactcctttaagaccccagggccgctggaggccttcgaggag
atcccagtggacgtggcggaggccgaggccttcctgcctggcttctcagcagaggcctgg
tgtaacgggctcccctaccccagccaggagcatggcccccaagtcctgggttcagaggtc
aaagtcaagcccccagttctggagagtggtgctgggatgttctgctaccagcctcccttg
cagcatatgtactgctcctcccagccccccttccaccagtactcgccaggtggtggcagc
taccccataccctacctgggctcctcacactatcagtaccagcgaatggcaccccaggcc
agcaccgatgggcaccagcctctcttcccaaaacccatctattcctacagcatcctcatc
ttcatggcccttaagaacagtaaaactgggagccttcccgtcagcgagatctacaatttt
atgacggagcactttccttacttcaagacagcacccgatggctggaagaattctgtccgg
cacaacctatccctcaacaagtgcttcgagaaggtggagaacaaatcaggaagttcctcc
cgcaagggctgcctgtgggccctcaatccggccaagatcgacaagatgcaagaggagctg
caaaaatggaagaggaaagatcccattgctgtgcgcaaaagcatggccaagccagaagag
ctggacagcctcattggagacaagagagaaaagctgggctccccactcctgggctgtccg
ccccctgggctgtccggctcaggccccatccggcccctggcacccccagctggcctctcc
ccaccactgcactcactccacccagctccaggccccattcctggcaagaaccccctgcag
gacctacttatggggcacacaccctcctgctatgggcagacatacttgcacctctcacca
ggcctggcccctcctggacccccgcagccattgttcccacagccggacgggcaccttgag
ctgcgggcccagccaggcaccccccaggactcgcctctgcctgcccacaccccacccagc
cacagtgccaagctactggccgagccttccccagccaggactatgcacgacaccctgctg
ccagatggagaccttggcactgacctggatgccatcaatccctcactcactgacttcgac
ttccagggaaacctgtgggaacagttgaaggatgatagcttggccctcgaccccctggta
ctggtgacctcatccccgacatcatcttcgatgccaccaccccagccaccacctcactgc
ttcccccctgggccctgtctgacagagacaggcagtggggcaggtgacttggcagccccg
ggcagtggtggctccggggcactgggtgacctgcacctcaccaccctctactctgccttt
atggagctggagcccacgccccccacggcccctgcaggcccctctgtgtacctcagcccc
agctccaagcccgtggccctggcatga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (26)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (24)   
DNA sequence (32)   
   RefSeq(nuc) (24)   
   GenBank (4)   
   EMBL (4)   
3D Structure (2)   
   PDB (2)   
Protein domain (1)   
   Pfam (1)   
All databases (84)   

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