Homo sapiens (human): 4487
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Homeodomain
Homeobox_KN
Motif
Other DBs
NCBI-GeneID:
4487
NCBI-ProteinID:
NP_002439
OMIM:
142983
HGNC:
7391
Ensembl:
ENSG00000163132
UniProt:
P28360
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All DBs
Position
4:4859665..4863936
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AA seq
303 aa
AA seq
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MAPAADMTSLPLGVKVEDSAFGKPAGGGAGQAPSAAAATAAAMGADEEGAKPKVSPSLLP
FSVEALMADHRKPGAKESALAPSEGVQAAGGSAQPLGVPPGSLGAPDAPSSPRPLGHFSV
GGLLKLPEDALVKAESPEKPERTPWMQSPRFSPPPARRLSPPACTLRKHKTNRKPRTPFT
TAQLLALERKFRQKQYLSIAERAEFSSSLSLTETQVKIWFQNRRAKAKRLQEAELEKLKM
AAKPMLPPAAFGLSFPLGGPAAVAAAAGASLYGASGPFQRAALPVAPVGLYTAHVGYSMY
HLT
NT seq
912 nt
NT seq
+upstream
nt +downstream
nt
atggccccggctgctgacatgacttctttgccactcggtgtcaaagtggaggactccgcc
ttcggcaagccggcggggggaggcgcgggccaggcccccagcgccgccgcggccacggca
gccgccatgggcgcggacgaggagggggccaagcccaaagtgtccccttcgctcctgccc
ttcagcgtggaggcgctcatggccgaccacaggaagccgggggccaaggagagcgccctg
gcgccctccgagggcgtgcaggcggcgggtggctcggcgcagccactgggcgtcccgccg
gggtcgctgggagccccggacgcgccctcttcgccgcggccgctcggccatttctcggtg
gggggactcctcaagctgccagaagatgcgctcgtcaaagccgagagccccgagaagccc
gagaggaccccgtggatgcagagcccccgcttctccccgccgccggccaggcggctgagc
cccccagcctgcaccctccgcaaacacaagacgaaccgtaagccgcggacgcccttcacc
accgcgcagctgctggcgctggagcgcaagttccgccagaagcagtacctgtccatcgcc
gagcgcgcggagttctccagctcgctcagcctcactgagacgcaggtgaagatatggttc
cagaaccgccgcgccaaggcaaagagactacaagaggcagagctggagaagctgaagatg
gccgccaagcccatgctgccaccggctgccttcggcctctccttccctctcggcggcccc
gcagctgtagcggccgcggcgggtgcctcgctctacggtgcctctggccccttccagcgc
gccgcgctgcctgtggcgcccgtgggactctacacggcccatgtgggctacagcatgtac
cacctgacatag
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