Homo sapiens (human): 5079
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Entry
5079 CDS
T01001
Symbol
PAX5, ALL3, BSAP, PAX-5
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PAX
Pax2_C
HTH_32
HTH_23
HTH_28
HTH_Tnp_IS1
Homeodomain
Motif
Other DBs
NCBI-GeneID:
5079
NCBI-ProteinID:
NP_057953
OMIM:
167414
HGNC:
8619
Ensembl:
ENSG00000196092
UniProt:
Q02548
Structure
PDB
LinkDB
All DBs
Position
9:complement(36833269..37034268)
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AA seq
391 aa
AA seq
DB search
MDLEKNYPTPRTSRTGHGGVNQLGGVFVNGRPLPDVVRQRIVELAHQGVRPCDISRQLRV
SHGCVSKILGRYYETGSIKPGVIGGSKPKVATPKVVEKIAEYKRQNPTMFAWEIRDRLLA
ERVCDNDTVPSVSSINRIIRTKVQQPPNQPVPASSHSIVSTGSVTQVSSVSTDSAGSSYS
ISGILGITSPSADTNKRKRDEGIQESPVPNGHSLPGRDFLRKQMRGDLFTQQQLEVLDRV
FERQHYSDIFTTTEPIKPEQTTEYSAMASLAGGLDDMKANLASPTPADIGSSVPGPQSYP
IVTGRDLASTTLPGYPPHVPPAGQGSYSAPTLTGMVPGSEFSGSPYSHPQYSSYNDSWRF
PNPGLLGSPYYYSAAARGAAPPAAATAYDRH
NT seq
1176 nt
NT seq
+upstream
nt +downstream
nt
atggatttagagaaaaattatccgactcctcggaccagcaggacaggacatggaggagtg
aatcagcttgggggggtttttgtgaatggacggccactcccggatgtagtccgccagagg
atagtggaacttgctcatcaaggtgtcaggccctgcgacatctccaggcagcttcgggtc
agccatggttgtgtcagcaaaattcttggcaggtattatgagacaggaagcatcaagcct
ggggtaattggaggatccaaaccaaaggtcgccacacccaaagtggtggaaaaaatcgct
gaatataaacgccaaaatcccaccatgtttgcctgggagatcagggaccggctgctggca
gagcgggtgtgtgacaatgacaccgtgcctagcgtcagttccatcaacaggatcatccgg
acaaaagtacagcagccacccaaccaaccagtcccagcttccagtcacagcatagtgtcc
actggctccgtgacgcaggtgtcctcggtgagcacggattcggccggctcgtcgtactcc
atcagcggcatcctgggcatcacgtcccccagcgccgacaccaacaagcgcaagagagac
gaaggtattcaggagtctccggtgccgaacggccactcgcttccgggcagagacttcctc
cggaagcagatgcggggagacttgttcacacagcagcagctggaggtgctggaccgcgtg
tttgagaggcagcactactcagacatcttcaccaccacagagcccatcaagcccgagcag
accacagagtattcagccatggcctcgctggctggtgggctggacgacatgaaggccaat
ctggccagccccacccctgctgacatcgggagcagtgtgccaggcccgcagtcctacccc
attgtgacaggccgtgacttggcgagcacgaccctccccgggtaccctccacacgtcccc
cccgctggacagggcagctactcagcaccgacgctgacagggatggtgcctgggagtgag
ttttccgggagtccctacagccaccctcagtattcctcgtacaacgactcctggaggttc
cccaacccggggctgcttggctccccctactattatagcgctgccgcccgaggagccgcc
ccacctgcagccgccactgcctatgaccgtcactga
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