KEGG   Homo sapiens (human): 7020
Entry
7020              CDS       T01001                                 
Symbol
TFAP2A, AP-2, AP-2alpha, AP2TF, BOFS, TFAP2
Name
(RefSeq) transcription factor AP-2 alpha
  KO
K09176  transcription factor AP-2 alpha/beta
Organism
hsa  Homo sapiens (human)
Disease
H00817  Branchiooculofacial syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    7020 (TFAP2A)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Other basic domains
   AP-2 (bHSH)
    7020 (TFAP2A)
SSDB
Motif
Pfam: TF_AP-2
Other DBs
NCBI-GeneID: 7020
NCBI-ProteinID: NP_001035890
OMIM: 107580
HGNC: 11742
Ensembl: ENSG00000137203
UniProt: P05549
Structure
Position
6:complement(10396677..10419659)
AA seq 433 aa
MSILAKMGDWQDRHDGTSNGTARLPQLGTVGQSPYTSAPPLSHTPNADFQPPYFPPPYQP
IYPQSQDPYSHVNDPYSLNPLHAQPQPQHPGWPGQRQSQESGLLHTHRGLPHQLSGLDPR
RDYRRHEDLLHGPHALSSGLGDLSIHSLPHAIEEVPHVEDPGINIPDQTVIKKGPVSLSK
SNSNAVSAIPINKDNLFGGVVNPNEVFCSVPGRLSLLSSTSKYKVTVAEVQRRLSPPECL
NASLLGGVLRRAKSKNGGRSLREKLDKIGLNLPAGRRKAANVTLLTSLVEGEAVHLARDF
GYVCETEFPAKAVAEFLNRQHSDPNEQVTRKNMLLATKQICKEFTDLLAQDRSPLGNSRP
NPILEPGIQSCLTHFNLISHGFGSPAVCAAVTALQNYLTEALKAMDKMYLSNNPNSHTDN
NAKSSDKEEKHRK
NT seq 1302 nt   +upstreamnt  +downstreamnt
atgtccatacttgccaaaatgggggactggcaggaccgtcacgacggcaccagcaacggg
acggcacggttgccccagctgggcactgtaggtcaatctccctacacgagcgccccgccg
ctgtcccacacccccaatgccgacttccagcccccatacttccccccaccctaccagcct
atctacccccagtcgcaagatccttactcccacgtcaacgacccctacagcctgaacccc
ctgcacgcccagccgcagccgcagcacccaggctggcccggccagaggcagagccaggag
tctgggctcctgcacacgcaccgggggctgcctcaccagctgtcgggcctggatcctcgc
agggactacaggcggcacgaggacctcctgcacggcccacacgcgctcagctcaggactc
ggagacctctcgatccactccttacctcacgccatcgaggaggtcccgcatgtagaagac
ccgggtattaacatcccagatcaaactgtaattaagaaaggccccgtgtccctgtccaag
tccaacagcaatgccgtctccgccatccctattaacaaggacaacctcttcggcggcgtg
gtgaaccccaacgaagtcttctgttcagttccgggtcgcctctcgctcctcagctccacc
tcgaagtacaaggtcacggtggcggaagtgcagcggcggctctcaccacccgagtgtctc
aacgcgtcgctgctgggcggagtgctccggagggcgaagtctaaaaatggaggaagatct
ttaagagaaaaactggacaaaataggattaaatctgcctgcagggagacgtaaagctgcc
aacgttaccctgctcacatcactagtagagggagaagctgtccacctagccagggacttt
gggtacgtgtgcgaaaccgaatttcctgccaaagcagtagctgaatttctcaaccgacaa
cattccgatcccaatgagcaagtgacaagaaaaaacatgctcctggctacaaaacagata
tgcaaagagttcaccgacctgctggctcaggaccgatctcccctggggaactcacggccc
aaccccatcctggagcccggcatccagagctgcttgacccacttcaacctcatctcccac
ggcttcggcagccccgcggtgtgtgccgcggtcacggccctgcagaactatctcaccgag
gccctcaaggccatggacaaaatgtacctcagcaacaaccccaacagccacacggacaac
aacgccaaaagcagtgacaaagaggagaagcacagaaagtga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (22)   
   RefSeq(nuc) (4)   
   GenBank (9)   
   EMBL (9)   
3D Structure (3)   
   PDB (3)   
Protein domain (1)   
   Pfam (1)   
All databases (51)   

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