KEGG   Homo sapiens (human): 145873
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)
SSDB
Motif
Pfam: HLH
Other DBs
NCBI-GeneID: 145873
NCBI-ProteinID: NP_001035047
OMIM: 605195
HGNC: 29659
Ensembl: ENSG00000188095
UniProt: Q0VG99
Position
15:89776332..89778754
AA seq 397 aa
MAQSPPPQSLLGHDHWIFAQGWGWAGHWDSTSPASSSDSSGSCPCDGARGLPQPQPPSCS
SRAAEAAATTPRRARTGPAGGQRQSASEREKLRMRTLARALHELRRFLPPSLAPAGQSLT
KIETLRLAIRYIGHLSAVLGLSEESLQCRRRQRGDAGSPWGCPLCPDRGPAEAQTQAEGQ
GQGQGQGQGQGQGQGQGQGQGQGQGRRPGLVSAVLAEASWGSPSACPGAQAAPERLGRGV
HDTDPWATPPYCPKIQSPPYSSQGTTSDASLWTPPQGCPWTQSSPEPRNPPVPWTAAPAT
LELAAVYQGLSVSPEPCLSLGAPSLLPHPSCQRLQPQTPGRCWSHSAEVVPNSEDQGPGA
AFQLSEASPPQSSGLRFSGCPELWQEDLEGARLGIFY
NT seq 1194 nt   +upstreamnt  +downstreamnt
atggcccagtcgcctcctccgcagagcctcctcggccacgaccactggatcttcgcccag
ggctggggctgggccggccactgggactccacgtccccggcctcctcctccgattcgtcg
ggttcgtgcccctgcgacggcgcccgcggactcccgcagccacagcctccgagctgcagc
tcccgagccgcagaggcagccgcgacgacgcccagacgagcgcgcaccggaccagcgggc
ggacagcggcagagcgccagcgagcgggagaaactgcgcatgcgcacgctggcccgcgcc
ctgcacgagttgcgccgctttctgcctccctccttggcgccggccggccagagcctgacc
aagatcgagacgctgcgcctggccatccgctacatcggccacctatcggccgtgctgggt
ctcagcgaggagagtctgcagtgccggcgcaggcagcgcggggacgcggggtccccttgg
ggctgcccgctgtgccccgaccgtggccccgcagaggcgcagacgcaggcggaggggcag
gggcaagggcaggggcaggggcaggggcaagggcaggggcaaggacaggggcaaggacag
gggcaagggcaggggcgcaggccgggcctggtctccgccgtcctcgccgaggcgtcctgg
ggatccccgtccgcctgccccggagcccaagccgcacccgagcgcctggggaggggggtc
cacgacacggatccctgggcaacacccccttactgccccaagatacagtcgcccccgtat
tcgtcccaagggacaacctccgacgcgtctctttggacgccaccccaaggctgtccctgg
acgcagtcgtccccagagccccggaacccaccagtgccctggacggcggccccagcaact
ttggagctggccgcagtgtaccagggtctctctgtgtctccagagccctgtctgtcgctg
ggagctccatctctcctgccccacccatcatgccagagactgcagcctcagacccccggg
aggtgctggagccacagtgcagaggtggtgcccaactcagaggaccagggaccgggcgcc
gccttccagctcagtgaagcaagccctccccagagctcaggcctgcggttcagtggctgc
cctgaactttggcaagaagatctggagggggcccgcctgggcatcttctactaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Network (2)   
   KEGG NETWORK (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (75)   
   KEGG ORTHOLOGY (1)   
   RefGene (69)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (5)   
   RefSeq(nuc) (1)   
   GenBank (2)   
   EMBL (2)   
Protein domain (1)   
   Pfam (1)   
All databases (93)   

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