KEGG   Homo sapiens (human): 5077
Entry
5077              CDS       T01001                                 
Symbol
PAX3, CDHS, HUP2, PAX-3, WS1, WS3
Name
(RefSeq) paired box 3
  KO
K09381  paired box protein 3/7
Organism
hsa  Homo sapiens (human)
Pathway
hsa05202  Transcriptional misregulation in cancer
Disease
H00037  Rhabdomyosarcoma
H00446  Craniofacial-deafness-hand syndrome
H00759  Waardenburg syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09161 Cancer: overview
   05202 Transcriptional misregulation in cancer
    5077 (PAX3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    5077 (PAX3)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    5077 (PAX3)
SSDB
Motif
Pfam: PAX Pax7 Homeodomain HTH_32 Homeobox_KN HTH_23 HTH_SB HTH_Tnp_IS1 DUF6033
Other DBs
NCBI-GeneID: 5077
NCBI-ProteinID: NP_852122
OMIM: 606597
HGNC: 8617
Ensembl: ENSG00000135903
UniProt: P23760
Structure
Position
2:complement(222199887..222298998)
AA seq 479 aa
MTTLAGAVPRMMRPGPGQNYPRSGFPLEVSTPLGQGRVNQLGGVFINGRPLPNHIRHKIV
EMAHHGIRPCVISRQLRVSHGCVSKILCRYQETGSIRPGAIGGSKPKQVTTPDVEKKIEE
YKRENPGMFSWEIRDKLLKDAVCDRNTVPSVSSISRILRSKFGKGEEEEADLERKEAEES
EKKAKHSIDGILSERASAPQSDEGSDIDSEPDLPLKRKQRRSRTTFTAEQLEELERAFER
THYPDIYTREELAQRAKLTEARVQVWFSNRRARWRKQAGANQLMAFNHLIPGGFPPTAMP
TLPTYQLSETSYQPTSIPQAVSDPSSTVHRPQPLPPSTVHQSTIPSNPDSSSAYCLPSTR
HGFSSYTDSFVPPSGPSNPMNPTIGNGLSPQVMGLLTNHGGVPHQPQTDYALSPLTGGLE
PTTTVSASCSQRLDHMKSLDSLPTSQSYCPPTYSTTGYSMDPVTGYQYGQYGQSKPWTF
NT seq 1440 nt   +upstreamnt  +downstreamnt
atgaccacgctggccggcgctgtgcccaggatgatgcggccgggcccggggcagaactac
ccgcgtagcgggttcccgctggaagtgtccactcccctcggccagggccgcgtcaaccag
ctcggcggtgtttttatcaacggcaggccgctgcccaaccacatccgccacaagatcgtg
gagatggcccaccacggcatccggccctgcgtcatctcgcgccagctgcgcgtgtcccac
ggctgcgtctccaagatcctgtgcaggtaccaggagactggctccatacgtcctggtgcc
atcggcggcagcaagcccaagcaggtgacaacgcctgacgtggagaagaaaattgaggaa
tacaaaagagagaacccgggcatgttcagctgggaaatccgagacaaattactcaaggac
gcggtctgtgatcgaaacaccgtgccgtcagtgagttccatcagccgcatcctgagaagt
aaattcgggaaaggtgaagaggaggaggccgacttggagaggaaggaggcagaggaaagc
gagaagaaggccaaacacagcatcgacggcatcctgagcgagcgagcctcagcaccccaa
tcagatgaaggctctgatattgactctgaaccagatttaccactaaagaggaaacagcgc
agaagccgaaccaccttcacagcagaacagctggaggaactggagcgtgcttttgagaga
actcattaccctgacatttatactagggaggaactggcccagagggcgaagctcaccgag
gcccgagtacaggtctggtttagcaaccgccgtgcaagatggaggaagcaagctggggcc
aatcaactgatggctttcaaccatctcattcccggggggttccctcccactgccatgccg
accttgccaacgtaccagctgtcggagacctcttaccagcccacatctattccacaagct
gtgtcagatcccagcagcaccgttcacagacctcaaccgcttcctccaagcactgtacac
caaagcacgattccttccaacccagacagcagctctgcctactgcctccccagcaccagg
catggattttccagctatacagacagctttgtgcctccgtcggggccctccaaccccatg
aaccccaccattggcaatggcctctcacctcaggtaatgggactcctgaccaaccacggt
ggggtacctcatcagccccagactgattacgcgctctcccctctcaccgggggtctggaa
cctaccaccacggtgtcggccagctgcagtcagagactagaccatatgaagagcttggac
agtctgccaacatctcagtcctactgtccacccacctatagcaccacaggctacagtatg
gaccctgtcacaggctaccaatatgggcagtatggacaaagtaagccttggactttttag

  All links  
Disease (5)   
   OMIM (5)   
Gene (9)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (10)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (8)   
DNA sequence (44)   
   RefSeq(nuc) (8)   
   GenBank (18)   
   EMBL (18)   
3D Structure (1)   
   PDB (1)   
Protein domain (9)   
   Pfam (9)   
All databases (78)   

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