KEGG   Homo sapiens (human): 5079
Entry
5079              CDS       T01001                                 

Symbol
PAX5, ALL3, BSAP
Name
(RefSeq) paired box 5
  KO
K09383  paired box protein 5
Organism
hsa  Homo sapiens (human)
Pathway
hsa05202  Transcriptional misregulation in cancer
Disease
H00001  B-cell acute lymphoblastic leukemia
H00011  Lymphoplasmacytic lymphoma
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09161 Cancer: overview
   05202 Transcriptional misregulation in cancer
    5079 (PAX5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    5079 (PAX5)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    5079 (PAX5)
SSDB
Motif
Pfam: PAX Pax2_C HTH_32 HTH_23 HTH_Tnp_IS1 HTH_28 Homeodomain
Other DBs
NCBI-GeneID: 5079
NCBI-ProteinID: NP_057953
OMIM: 167414
HGNC: 8619
Ensembl: ENSG00000196092
Vega: OTTHUMG00000019907
Pharos: Q02548(Tbio)
UniProt: Q02548
Structure
PDB: 
1K78 1MDM

Position
9p13.2
AA seq 391 aa
MDLEKNYPTPRTSRTGHGGVNQLGGVFVNGRPLPDVVRQRIVELAHQGVRPCDISRQLRV
SHGCVSKILGRYYETGSIKPGVIGGSKPKVATPKVVEKIAEYKRQNPTMFAWEIRDRLLA
ERVCDNDTVPSVSSINRIIRTKVQQPPNQPVPASSHSIVSTGSVTQVSSVSTDSAGSSYS
ISGILGITSPSADTNKRKRDEGIQESPVPNGHSLPGRDFLRKQMRGDLFTQQQLEVLDRV
FERQHYSDIFTTTEPIKPEQTTEYSAMASLAGGLDDMKANLASPTPADIGSSVPGPQSYP
IVTGRDLASTTLPGYPPHVPPAGQGSYSAPTLTGMVPGSEFSGSPYSHPQYSSYNDSWRF
PNPGLLGSPYYYSAAARGAAPPAAATAYDRH
NT seq 1176 nt   +upstreamnt  +downstreamnt
atggatttagagaaaaattatccgactcctcggaccagcaggacaggacatggaggagtg
aatcagcttgggggggtttttgtgaatggacggccactcccggatgtagtccgccagagg
atagtggaacttgctcatcaaggtgtcaggccctgcgacatctccaggcagcttcgggtc
agccatggttgtgtcagcaaaattcttggcaggtattatgagacaggaagcatcaagcct
ggggtaattggaggatccaaaccaaaggtcgccacacccaaagtggtggaaaaaatcgct
gaatataaacgccaaaatcccaccatgtttgcctgggagatcagggaccggctgctggca
gagcgggtgtgtgacaatgacaccgtgcctagcgtcagttccatcaacaggatcatccgg
acaaaagtacagcagccacccaaccaaccagtcccagcttccagtcacagcatagtgtcc
actggctccgtgacgcaggtgtcctcggtgagcacggattcggccggctcgtcgtactcc
atcagcggcatcctgggcatcacgtcccccagcgccgacaccaacaagcgcaagagagac
gaaggtattcaggagtctccggtgccgaacggccactcgcttccgggcagagacttcctc
cggaagcagatgcggggagacttgttcacacagcagcagctggaggtgctggaccgcgtg
tttgagaggcagcactactcagacatcttcaccaccacagagcccatcaagcccgagcag
accacagagtattcagccatggcctcgctggctggtgggctggacgacatgaaggccaat
ctggccagccccacccctgctgacatcgggagcagtgtgccaggcccgcagtcctacccc
attgtgacaggccgtgacttggcgagcacgaccctccccgggtaccctccacacgtcccc
cccgctggacagggcagctactcagcaccgacgctgacagggatggtgcctgggagtgag
ttttccgggagtccctacagccaccctcagtattcctcgtacaacgactcctggaggttc
cccaacccggggctgcttggctccccctactattatagcgctgccgcccgaggagccgcc
ccacctgcagccgccactgcctatgaccgtcactga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (4)   
   KEGG DISEASE (2)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (9)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
   PHAROS (1)   
   VEGA (1)   
Protein sequence (13)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (11)   
DNA sequence (73)   
   RefSeq(nuc) (13)   
   GenBank (30)   
   EMBL (30)   
Protein domain (7)   
   Pfam (7)   
All databases (110)   

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