KEGG   Monodelphis domestica (gray short-tailed opossum): 100617787
Entry
100617787         CDS       T01031                                 
Symbol
DVL2
Name
(RefSeq) dishevelled segment polarity protein 2
  KO
K02353  segment polarity protein dishevelled
Organism
mdo  Monodelphis domestica (gray short-tailed opossum)
Pathway
mdo04150  mTOR signaling pathway
mdo04310  Wnt signaling pathway
mdo04330  Notch signaling pathway
mdo04390  Hippo signaling pathway
mdo04550  Signaling pathways regulating pluripotency of stem cells
mdo04916  Melanogenesis
mdo04934  Cushing syndrome
mdo05010  Alzheimer disease
mdo05022  Pathways of neurodegeneration - multiple diseases
mdo05165  Human papillomavirus infection
mdo05200  Pathways in cancer
mdo05217  Basal cell carcinoma
mdo05224  Breast cancer
mdo05225  Hepatocellular carcinoma
mdo05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mdo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100617787 (DVL2)
   04330 Notch signaling pathway
    100617787 (DVL2)
   04390 Hippo signaling pathway
    100617787 (DVL2)
   04150 mTOR signaling pathway
    100617787 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100617787 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100617787 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100617787 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100617787 (DVL2)
   05226 Gastric cancer
    100617787 (DVL2)
   05217 Basal cell carcinoma
    100617787 (DVL2)
   05224 Breast cancer
    100617787 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100617787 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100617787 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    100617787 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100617787 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100617787
NCBI-ProteinID: XP_003340373
Ensembl: ENSMODG00000006553
LinkDB
Position
2:255542918..255549844
AA seq 736 aa
MAGSSAAGLGGAGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYYFKS
MDQDFGVVKEEISDDNARLPCFNGRVVLLGKVSXLVSSDNPQPENTPQAPEPRAEPSSPP
PPLPPLPPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVISLRRDRSRRRESIDHVG
GGHRPNGSSRLERHLAGYESSSTLLTSELENTSLGDSDEDDTMSRFSSSTEQSSASRLLK
RHRRRRKQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGI
YIGSIMKGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLREIVHKPGPIVLTVAKC
WDPSPQAYFTLPRNEPIQPIDPAAWVSHSAALTGAFPAYPGSSSMSTITSGSSLPDGCEG
RSLSIHTDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERRE
ARKYASGLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQD
TLAPLPGATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYSYGGGSAGSQHSEGSRSSGS
TRSDGGIGRPGRPEDRGPESKSGSGSESEPSSRGGSLHWGGDSGDATPPPPRGLGGGGSS
LRSHPNLHPYGPPPGVALPYNPMMVVMMPPPPPPAVQPPGAPPVRDLGSVPPELTASRQS
FHLAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcagcgccgctggactcggtggggctggcgagacgaaggtgatttaccat
ctggacgaggaggagacgccgtacctggtcaagatcccggtcccggccgagcgcatcacc
ttaggagactttaagagcgtcctgcagcgccccgccggggccaagtactacttcaagtca
atggaccaggattttggagtggtgaaggaggagatttcagatgacaatgcccgattgccc
tgcttcaatgggagggtagtcctcttgggtaaggtgtcttgacttgtgtcctcagataac
cctcagccagagaacaccccccaagctcctgagcctcgagcagaaccctcatctccaccc
ccaccactgcctcccctccctcctgagaggactagtggcattggggactcaaggcctcca
tctttccaccctaatgtatctagcagccgagaaaacctagagcctgagacagaaacagaa
tcagtaatatcactgagacgggatcggtctaggaggagagaaagcatcgatcatgttggt
ggtggccaccgacctaatggttcttcccgattggagcggcacctggctggttatgagagc
tcctctactctcttaactagtgaactagagaacaccagcctaggagattcagatgaggat
gataccatgagcaggttcagtagctccaccgagcagagcagtgcctcccgactcttaaag
agacaccgtcggaggaggaaacagcgaccacctcgactagaaaggacctcatccttcagc
agtgtaacagattctaccatgtctctcaatatcatcacagtcacgctcaacatggagaag
tacaatttcctgggcatctccattgtgggccaaagcaatgagcgtggcgatggtggcatc
tacatcggctccatcatgaagggtggtgctgtggctgcagatgggcgaattgaaccaggg
gacatgctgctgcaggtgaatgacatgaactttgagaacatgagtaatgatgatgccgta
cgggtgctaagagagattgtgcacaagcctggccccatcgtgttaactgtggccaaatgc
tgggatccctcccctcaggcttacttcacactcccccgaaatgagccaatccagcctatt
gaccctgcggcctgggtttcccattcagcagcactcactggtgccttccctgcctaccca
ggctcttcttctatgagcactataacttcaggctcttccctgcctgatggttgtgaagga
cgtagcctctctatacacacagacatggcatctgtgaccaaggccatggcagcgcctgag
tctgggctggaggtccgggatcgaatgtggcttaagataactattcccaatgcctttctg
ggctcagatgtagtcgactggctttaccaccatgtggaagggttccctgaacgtcgggag
gcaaggaaatatgccagtgggttgctcaaggcaggcctaatccggcatactgtcaacaag
atcaccttttctgaacagtgttactatgtcttcggggacctcagtgggggctgtgaaagc
taccttgtgaacctctctctgaatgataatgatggatcaagtggagcttctgaccaggac
acactggctccactgcctggggccacaccatggcccttgctacctactttctcctaccag
tatccagccccacatccctatagtccccaacctcccccttatcatgagctttcatcctat
agctatggagggggcagtgctggcagccagcatagtgagggaagccggagcagtggatct
acacgaagtgatgggggcataggacgtcctgggaggccagaagatcgaggtccggaatcc
aaatcaggcagtggtagtgaatcagagccatcaagccgtggtggtagccttcactggggt
ggggattctggtgatgccacccctcctccacccaggggactaggtgggggtggcagcagc
cttcgttctcaccctaatctccatccctatgggccgcctcctggtgtggcactaccatat
aaccccatgatggtagttatgatgccacctccaccccccccagcagttcagcctcctgga
gcacctcctgttcgagacctgggctctgtaccacctgagctaactgccagtcgacagagc
ttccacctggccatgggcaaccctagtgagttttttgtggatgtcatgtag

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