Homo sapiens (human): 145873
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Entry
145873 CDS
T01001
Symbol
MESP2, SCDO2, bHLHc6
Name
(RefSeq) mesoderm posterior bHLH transcription factor 2
KO
K09076
mesoderm posterior
Organism
hsa
Homo sapiens (human)
Network
nt06511
NOTCH signaling
Element
N01481
Notch-MESP2 signaling
Disease
H00517
Spondylocostal dysostosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
145873 (MESP2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Tal/Twist/Atonal/Hen, Mesp
145873 (MESP2)
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Gene cluster
GFIT
Motif
Pfam:
HLH
TrAA12
Motif
Other DBs
NCBI-GeneID:
145873
NCBI-ProteinID:
NP_001035047
OMIM:
605195
HGNC:
29659
Ensembl:
ENSG00000188095
UniProt:
Q0VG99
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Position
15:89776332..89778754
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AA seq
397 aa
AA seq
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MAQSPPPQSLLGHDHWIFAQGWGWAGHWDSTSPASSSDSSGSCPCDGARGLPQPQPPSCS
SRAAEAAATTPRRARTGPAGGQRQSASEREKLRMRTLARALHELRRFLPPSLAPAGQSLT
KIETLRLAIRYIGHLSAVLGLSEESLQCRRRQRGDAGSPWGCPLCPDRGPAEAQTQAEGQ
GQGQGQGQGQGQGQGQGQGQGQGQGRRPGLVSAVLAEASWGSPSACPGAQAAPERLGRGV
HDTDPWATPPYCPKIQSPPYSSQGTTSDASLWTPPQGCPWTQSSPEPRNPPVPWTAAPAT
LELAAVYQGLSVSPEPCLSLGAPSLLPHPSCQRLQPQTPGRCWSHSAEVVPNSEDQGPGA
AFQLSEASPPQSSGLRFSGCPELWQEDLEGARLGIFY
NT seq
1194 nt
NT seq
+upstream
nt +downstream
nt
atggcccagtcgcctcctccgcagagcctcctcggccacgaccactggatcttcgcccag
ggctggggctgggccggccactgggactccacgtccccggcctcctcctccgattcgtcg
ggttcgtgcccctgcgacggcgcccgcggactcccgcagccacagcctccgagctgcagc
tcccgagccgcagaggcagccgcgacgacgcccagacgagcgcgcaccggaccagcgggc
ggacagcggcagagcgccagcgagcgggagaaactgcgcatgcgcacgctggcccgcgcc
ctgcacgagttgcgccgctttctgcctccctccttggcgccggccggccagagcctgacc
aagatcgagacgctgcgcctggccatccgctacatcggccacctatcggccgtgctgggt
ctcagcgaggagagtctgcagtgccggcgcaggcagcgcggggacgcggggtccccttgg
ggctgcccgctgtgccccgaccgtggccccgcagaggcgcagacgcaggcggaggggcag
gggcaagggcaggggcaggggcaggggcaagggcaggggcaaggacaggggcaaggacag
gggcaagggcaggggcgcaggccgggcctggtctccgccgtcctcgccgaggcgtcctgg
ggatccccgtccgcctgccccggagcccaagccgcacccgagcgcctggggaggggggtc
cacgacacggatccctgggcaacacccccttactgccccaagatacagtcgcccccgtat
tcgtcccaagggacaacctccgacgcgtctctttggacgccaccccaaggctgtccctgg
acgcagtcgtccccagagccccggaacccaccagtgccctggacggcggccccagcaact
ttggagctggccgcagtgtaccagggtctctctgtgtctccagagccctgtctgtcgctg
ggagctccatctctcctgccccacccatcatgccagagactgcagcctcagacccccggg
aggtgctggagccacagtgcagaggtggtgcccaactcagaggaccagggaccgggcgcc
gccttccagctcagtgaagcaagccctccccagagctcaggcctgcggttcagtggctgc
cctgaactttggcaagaagatctggagggggcccgcctgggcatcttctactaa
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