KEGG   Homo sapiens (human): 3211
Entry
3211              CDS       T01001                                 
Symbol
HOXB1, HCFP3, HOX2, HOX2I, Hox-2.9
Name
(RefSeq) homeobox B1
  KO
K09301  homeobox protein HoxA/B/D1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04550  Signaling pathways regulating pluripotency of stem cells
Disease
H02151  Hereditary congenital facial paresis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    3211 (HOXB1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    3211 (HOXB1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: HOXL
    3211 (HOXB1)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN
Other DBs
NCBI-GeneID: 3211
NCBI-ProteinID: NP_002135
OMIM: 142968
HGNC: 5111
Ensembl: ENSG00000120094
UniProt: P14653
Structure
Position
17:complement(48528526..48531011)
AA seq 301 aa
MDYNRMNSFLEYPLCNRGPSAYSAHSAPTSFPPSSAQAVDSYASEGRYGGGLSSPAFQQN
SGYPAQQPPSTLGVPFPSSAPSGYAPAACSPSYGPSQYYPLGQSEGDGGYFHPSSYGAQL
GGLSDGYGAGGAGPGPYPPQHPPYGNEQTASFAPAYADLLSEDKETPCPSEPNTPTARTF
DWMKVKRNPPKTAKVSEPGLGSPSGLRTNFTTRQLTELEKEFHFNKYLSRARRVEIAATL
ELNETQVKIWFQNRRMKQKKREREEGRVPPAPPGCPKEAAGDASDQSTCTSPEASPSSVT
S
NT seq 906 nt   +upstreamnt  +downstreamnt
atggactataataggatgaactccttcttagagtacccactctgtaaccggggacccagc
gcctacagcgcccacagcgccccaacctcctttcccccaagctcggctcaggcggttgac
agctatgcaagcgagggccgctacggtggggggctgtccagccctgcgtttcagcagaac
tccggctatcccgcccagcagccgccttcgaccctgggggtgcccttccccagctccgcg
ccctcggggtatgctcctgccgcctgcagccccagctacgggccttctcagtactaccct
ctgggtcaatcagaaggagacggaggctattttcatccctcgagctacggggcccagcta
gggggcttgtccgatggctacggagcaggtggagccggtccggggccatatcctccgcag
catcccccttatgggaacgagcagaccgcgagctttgcaccggcctatgctgatctcctc
tccgaggacaaggaaacaccctgcccttcagaacctaacacccccacggcccggaccttc
gactggatgaaggttaagagaaacccacccaagacagcgaaggtgtcagagccaggcctg
ggctcgcccagtggcctccgcaccaacttcaccacaaggcagctgacagaactggaaaag
gagttccatttcaacaagtacctgagccgggcccggagggtggagattgccgccaccctg
gagctcaatgaaacacaggtcaagatttggttccagaaccgacgaatgaagcagaagaag
cgcgagcgagaggaaggtcgggtccccccagccccaccaggctgccccaaggaggcagct
ggagatgcctcagaccagtcgacatgcacctccccggaagcctcacccagctctgtcacc
tcctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (25)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
   PRONIT (16)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (11)   
   RefSeq(nuc) (1)   
   GenBank (5)   
   EMBL (5)   
3D Structure (1)   
   PDB (1)   
Protein domain (2)   
   Pfam (2)   
All databases (49)   

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