KEGG   Homo sapiens (human): 668
Entry
668               CDS       T01001                                 
Symbol
FOXL2, BPES, BPES1, PFRK, PINTO, POF3
Name
(RefSeq) forkhead box L2
  KO
K09405  forkhead box protein L
Organism
hsa  Homo sapiens (human)
Disease
H00627  Premature ovarian failure
H00826  Blepharophimosis-ptosis-epicanthus inversus syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    668 (FOXL2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Fork head/winged helix other regulators
    668 (FOXL2)
SSDB
Motif
Pfam: Forkhead
Other DBs
NCBI-GeneID: 668
NCBI-ProteinID: NP_075555
OMIM: 605597
HGNC: 1092
Ensembl: ENSG00000183770
UniProt: P58012 Q53ZD3
Structure
Position
3:complement(138944224..138947137)
AA seq 376 aa
MMASYPEPEDAAGALLAPETGRTVKEPEGPPPSPGKGGGGGGGTAPEKPDPAQKPPYSYV
ALIAMAIRESAEKRLTLSGIYQYIIAKFPFYEKNKKGWQNSIRHNLSLNECFIKVPREGG
GERKGNYWTLDPACEDMFEKGNYRRRRRMKRPFRPPPAHFQPGKGLFGAGGAAGGCGVAG
AGADGYGYLAPPKYLQSGFLNNSWPLPQPPSPMPYASCQMAAAAAAAAAAAAAAGPGSPG
AAAVVKGLAGPAASYGPYTRVQSMALPPGVVNSYNGLGGPPAAPPPPPHPHPHPHAHHLH
AAAAPPPAPPHHGAAAPPPGQLSPASPATAAPPAPAPTSAPGLQFACARQPELAMMHCSY
WDHDSKTGALHSRLDL
NT seq 1131 nt   +upstreamnt  +downstreamnt
atgatggccagctaccccgagcccgaggacgcggcgggggccctgctggccccagagacc
ggtcgcacagtcaaggagccagaagggccgccgccgagcccaggcaagggcggtgggggt
ggcggcgggacagccccggagaagccggacccggcgcagaagcccccgtactcgtacgtg
gcgctcatcgccatggcgatccgcgagagcgcggagaagaggctcacgctgtccggcatc
taccagtacatcatcgcgaagttcccgttctacgagaagaataagaagggctggcaaaat
agcatccgccacaacctcagcctcaacgagtgcttcatcaaggtgccgcgcgagggcggc
ggcgagcgcaagggcaactactggacgctggacccggcctgcgaagacatgttcgagaag
ggcaactaccggcgccgccgccgcatgaagaggcccttccggccgccgcccgcgcacttc
cagcccggcaaggggctcttcggggccggaggcgccgcaggcgggtgcggcgtggcgggc
gccggggccgacggctacggctacctggcgccccccaagtacctgcagtctggcttcctc
aacaactcgtggccgctaccgcagcctccctcacccatgccctatgcctcctgccagatg
gcggcagccgcagcggctgcagcagctgcggctgcagccgcgggccccggtagccctggc
gcggccgctgtggtcaaggggctggcgggcccggccgcctcgtacgggccgtacacacgc
gtgcagagcatggcgctgccccccggcgtagtgaactcgtacaatggcctgggaggcccg
ccggccgcacccccgcctccgccgcacccccacccgcatccgcacgcacaccatctgcac
gcggccgccgcaccgccgcctgccccaccgcaccacggggccgccgcgccgccgccgggc
cagctcagccctgccagcccagccaccgccgcgcccccggcgcccgcgcccaccagtgcg
ccgggcctgcagttcgcttgtgcccggcagcccgagctcgccatgatgcattgctcttac
tgggaccacgacagcaagaccggcgcgctgcattcgcgcctcgatctctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (30)   
   KEGG ORTHOLOGY (1)   
   RefGene (21)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (4)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (55)   
   RefSeq(nuc) (1)   
   GenBank (27)   
   EMBL (27)   
3D Structure (2)   
   PDB (2)   
Protein domain (1)   
   Pfam (1)   
All databases (100)   

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