KEGG   Homo sapiens (human): 4487
Entry
4487              CDS       T01001                                 
Symbol
MSX1, ECTD3, HOX7, HYD1, STHAG1
Name
(RefSeq) msh homeobox 1
  KO
K09341  homeobox protein MSX
Organism
hsa  Homo sapiens (human)
Pathway
hsa05166  Human T-cell leukemia virus 1 infection
Disease
H00516  Cleft lip and/or cleft palate
H00625  Tooth agenesis
H00643  Tooth and nail syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    4487 (MSX1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4487 (MSX1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: NKL
    4487 (MSX1)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN
Other DBs
NCBI-GeneID: 4487
NCBI-ProteinID: NP_002439
OMIM: 142983
HGNC: 7391
Ensembl: ENSG00000163132
UniProt: P28360
Position
4:4859665..4863936
AA seq 303 aa
MAPAADMTSLPLGVKVEDSAFGKPAGGGAGQAPSAAAATAAAMGADEEGAKPKVSPSLLP
FSVEALMADHRKPGAKESALAPSEGVQAAGGSAQPLGVPPGSLGAPDAPSSPRPLGHFSV
GGLLKLPEDALVKAESPEKPERTPWMQSPRFSPPPARRLSPPACTLRKHKTNRKPRTPFT
TAQLLALERKFRQKQYLSIAERAEFSSSLSLTETQVKIWFQNRRAKAKRLQEAELEKLKM
AAKPMLPPAAFGLSFPLGGPAAVAAAAGASLYGASGPFQRAALPVAPVGLYTAHVGYSMY
HLT
NT seq 912 nt   +upstreamnt  +downstreamnt
atggccccggctgctgacatgacttctttgccactcggtgtcaaagtggaggactccgcc
ttcggcaagccggcggggggaggcgcgggccaggcccccagcgccgccgcggccacggca
gccgccatgggcgcggacgaggagggggccaagcccaaagtgtccccttcgctcctgccc
ttcagcgtggaggcgctcatggccgaccacaggaagccgggggccaaggagagcgccctg
gcgccctccgagggcgtgcaggcggcgggtggctcggcgcagccactgggcgtcccgccg
gggtcgctgggagccccggacgcgccctcttcgccgcggccgctcggccatttctcggtg
gggggactcctcaagctgccagaagatgcgctcgtcaaagccgagagccccgagaagccc
gagaggaccccgtggatgcagagcccccgcttctccccgccgccggccaggcggctgagc
cccccagcctgcaccctccgcaaacacaagacgaaccgtaagccgcggacgcccttcacc
accgcgcagctgctggcgctggagcgcaagttccgccagaagcagtacctgtccatcgcc
gagcgcgcggagttctccagctcgctcagcctcactgagacgcaggtgaagatatggttc
cagaaccgccgcgccaaggcaaagagactacaagaggcagagctggagaagctgaagatg
gccgccaagcccatgctgccaccggctgccttcggcctctccttccctctcggcggcccc
gcagctgtagcggccgcggcgggtgcctcgctctacggtgcctctggccccttccagcgc
gccgcgctgcctgtggcgcccgtgggactctacacggcccatgtgggctacagcatgtac
cacctgacatag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (7)   
   KEGG DISEASE (3)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (15)   
   RefSeq(nuc) (1)   
   GenBank (7)   
   EMBL (7)   
Protein domain (2)   
   Pfam (2)   
All databases (45)   

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