KEGG   Homo sapiens (human): 8929
Entry
8929              CDS       T01001                                 
Symbol
PHOX2B, CCHS, NBLST2, NBPhox, PMX2B
Name
(RefSeq) paired like homeobox 2B
  KO
K09330  paired mesoderm homeobox protein 2
Organism
hsa  Homo sapiens (human)
Disease
H00043  Neuroblastoma
H00916  Congenital central hypoventilation syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    8929 (PHOX2B)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    8929 (PHOX2B)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN CIS_TMP
Other DBs
NCBI-GeneID: 8929
NCBI-ProteinID: NP_003915
OMIM: 603851
HGNC: 9143
Ensembl: ENSG00000109132
UniProt: Q99453
Structure
Position
4:complement(41744082..41748725)
AA seq 314 aa
MYKMEYSYLNSSAYESCMAGMDTSSLASAYADFSSCSQASGFQYNPIRTTFGATSGCPSL
TPGSCSLGTLRDHQSSPYAAVPYKLFTDHGGLNEKRKQRRIRTTFTSAQLKELERVFAET
HYPDIYTREELALKIDLTEARVQVWFQNRRAKFRKQERAAAAAAAAAKNGSSGKKSDSSR
DDESKEAKSTDPDSTGGPGPNPNPTPSCGANGGGGGGPSPAGAPGAAGPGGPGGEPGKGG
AAAAAAAAAAAAAAAAAAAAGGLAAAGGPGQGWAPGPGPITSIPDSLGGPFASVLSSLQR
PNGAKAALVKSSMF
NT seq 945 nt   +upstreamnt  +downstreamnt
atgtataaaatggaatattcttacctcaattcctctgcctacgagtcctgtatggctggg
atggacacctcgagcctggcttcagcctatgctgacttcagttcctgcagccaggccagt
ggcttccagtataacccgataaggaccacttttggggccacgtccggctgcccttccctc
acgccgggatcctgcagcctgggcaccctcagggaccaccagagcagtccgtacgccgca
gttccttacaaactcttcacggaccacggcggcctcaacgagaagcgcaagcagcggcgc
atccgcaccactttcaccagtgcccagctcaaagagctggaaagggtcttcgcggagact
cactaccccgacatctacactcgggaggagctggccctgaagatcgacctcacagaggcg
cgagtccaggtgtggttccagaaccgccgcgccaagtttcgcaagcaggagcgcgcagcg
gcagccgcagcggccgcggccaagaacggctcctcgggcaaaaagtctgactcttccagg
gacgacgagagcaaagaggccaagagcactgacccggacagcactgggggcccaggtccc
aatcccaaccccacccccagctgcggggcgaatggaggcggcggcggcgggcccagcccg
gctggagctccgggggcggcggggcccgggggcccgggaggcgaacccggcaagggcggc
gcagcagcagcggcggcggccgcggcagcggcggcggcggcagcggcagcggcggcagct
ggaggcctggctgcggctgggggccctggacaaggctgggctcccggccccggccccatc
acctccatcccggattcgcttgggggtcccttcgccagcgtcctatcttcgctccaaaga
cccaacggtgccaaagccgccttagtgaagagcagtatgttctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (23)   
   KEGG ORTHOLOGY (1)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (25)   
   RefSeq(nuc) (1)   
   GenBank (12)   
   EMBL (12)   
3D Structure (2)   
   PDB (2)   
Protein domain (3)   
   Pfam (3)   
All databases (64)   

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