KEGG   Homo sapiens (human): 442425
Entry
442425            CDS       T01001                                 
Symbol
FOXB2, FKH4, bA159H20.4
Name
(RefSeq) forkhead box B2
  KO
K09395  forkhead box protein B
Organism
hsa  Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    442425 (FOXB2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Fork head/winged helix other regulators
    442425 (FOXB2)
SSDB
Motif
Pfam: Forkhead
Other DBs
NCBI-GeneID: 442425
NCBI-ProteinID: NP_001013757
OMIM: 619962
HGNC: 23315
Ensembl: ENSG00000204612
UniProt: Q5VYV0
Position
9:77019655..77020953
AA seq 432 aa
MPRPGKSSYSDQKPPYSYISLTAMAIQHSAEKMLPLSDIYKFIMERFPYYREHTQRWQNS
LRHNLSFNDCFIKIPRRPDQPGKGSFWALHPDCGDMFENGSFLRRRKRFKVLRADHTHLH
AGSTKSAPGAGPGGHLHPHHHHHPHHHHHHHAAAHHHHHHHPPQPPPPPPPPPPHMVHYF
HQQPPTAPQPPPHLPSQPPQQPPQQSQPQQPSHPGKMQEAAAVAAAAAAAAAAAVGSVGR
LSQFPPYGLGSAAAAAAAAAASTSGFKHPFAIENIIGRDYKGVLQAGGLPLASVMHHLGY
PVPGQLGNVVSSVWPHVGVMDSVAAAAAAAAAAGVPVGPEYGAFGVPVKSLCHSASQSLP
AMPVPIKPTPALPPVSALQPGLTVPAASQQPPAPSTVCSAAAASPVASLLEPTAPTSAES
KGGSLHSVLVHS
NT seq 1299 nt   +upstreamnt  +downstreamnt
atgccgcggccggggaagagctcgtacagcgaccaaaaaccgccctactcttacatctcg
ctgaccgccatggcaatccagcactcggccgagaagatgctgccgctgagcgacatctac
aagttcatcatggagcgcttcccctactaccgcgagcacacacagcgctggcagaacagc
ctgcgccacaacctctccttcaacgactgcttcatcaagattccgcggaggcccgaccag
cctggcaagggtagcttctgggcgctgcaccccgactgcggggacatgttcgagaacggc
agcttcctgcggcgtcgcaagcgcttcaaggtgctgcgcgccgaccatactcacttgcac
gcgggaagcaccaagagcgcgccgggcgccggtccgggagggcaccttcacccccatcac
caccaccacccccaccaccaccatcatcaccacgctgccgcacaccaccaccatcaccac
cacccaccccagccgccgccgccgccgcccccgccgccgccgcacatggtacactatttc
catcagcaaccgcctactgctccgcagccgcctccgcacctcccgtcacagcccccgcag
caaccgccccagcagtcgcagcctcagcagccgtctcaccccggcaagatgcaggaggcg
gcggccgtggcggcggcggcggcggcggccgcggcagccgcggtgggcagcgtgggacgc
ctgtctcagttcccaccctacgggctgggctcggccgccgccgctgccgccgcggccgcg
gcgtccacgtcaggcttcaagcacccctttgccattgagaacattattggccgggactac
aagggcgtgctgcaggctggagggctgcccttggcgtccgtcatgcaccacctgggctac
cccgtgcccggccagcttggcaacgtcgtcagctccgtgtggccgcacgttggcgtcatg
gattcggtggccgccgccgcggccgccgcagccgcagccggagtccctgtaggcccggag
tatggggccttcggggtcccggtcaagtccctgtgccactcggcaagccagagcctgcct
gccatgccggtgcccatcaagcccacgcctgcgctgccgcccgtgtccgcgctgcagccg
gggctcactgtccccgcggcttcgcagcagcctccggcgccatccaccgtgtgctccgcg
gccgcggcctcgcccgttgcctctctgctggagcccacagcccctacctcggccgaaagc
aagggcggctccttgcactcggtgctagtgcactcctag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (39)   
   KEGG ORTHOLOGY (1)   
   RefGene (33)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (1)   
   RefSeq(nuc) (1)   
Protein domain (1)   
   Pfam (1)   
All databases (48)   

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