KEGG   Peromyscus leucopus (white-footed mouse): 114683308
Entry
114683308         CDS       T07241                                 
Symbol
Dvl3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
pleu  Peromyscus leucopus (white-footed mouse)
Pathway
pleu04150  mTOR signaling pathway
pleu04310  Wnt signaling pathway
pleu04330  Notch signaling pathway
pleu04390  Hippo signaling pathway
pleu04550  Signaling pathways regulating pluripotency of stem cells
pleu04916  Melanogenesis
pleu04934  Cushing syndrome
pleu05010  Alzheimer disease
pleu05022  Pathways of neurodegeneration - multiple diseases
pleu05165  Human papillomavirus infection
pleu05200  Pathways in cancer
pleu05217  Basal cell carcinoma
pleu05224  Breast cancer
pleu05225  Hepatocellular carcinoma
pleu05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pleu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    114683308 (Dvl3)
   04330 Notch signaling pathway
    114683308 (Dvl3)
   04390 Hippo signaling pathway
    114683308 (Dvl3)
   04150 mTOR signaling pathway
    114683308 (Dvl3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    114683308 (Dvl3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    114683308 (Dvl3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    114683308 (Dvl3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    114683308 (Dvl3)
   05226 Gastric cancer
    114683308 (Dvl3)
   05217 Basal cell carcinoma
    114683308 (Dvl3)
   05224 Breast cancer
    114683308 (Dvl3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    114683308 (Dvl3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    114683308 (Dvl3)
   05022 Pathways of neurodegeneration - multiple diseases
    114683308 (Dvl3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    114683308 (Dvl3)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 114683308
NCBI-ProteinID: XP_028713372
LinkDB
Position
12:complement(77009035..77023813)
AA seq 713 aa
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPEPAPFCADNPSELPPSIERTGGIGDSRPPSFHPH
ASGGSQENLDNDTETDSLVSAQRERPRRRDGPEHAARLNGTAKGERRREPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAA
WVSHTAAMTGTFPAYGMSPSLSTITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMA
SPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHT
VNKITFSEQCYYIFGDLCGNMANLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQY
PPPPHPYNPHPGFPELGYSYGGGGGSASSQHSEGSRSSGSNRSGSDRRKEKDPKAGDSKS
GGSGSESDHTTRSSLRGPRERAPSERSGPAASEHSHRSLRSHHTHPSYGPPGVPPLYGPP
MLMMTPPPAAMGPPGAPPGRDLASVPPELTASRQSFRMAMGNPTKNFGLFDFL
NT seq 2142 nt   +upstreamnt  +downstreamnt
atgggcgagaccaagatcatctaccacctggacgggcaggagacgccgtacctggtgaag
ctgcccctgcccgccgagcgcgtcaccttggcggactttaagggcgttctgcagcggccc
agctataagttcttcttcaagtctatggatgacgattttggggtggtgaaggaagagatc
tccgacgacaatgccaagctaccctgcttcaatggccgagtggtgtcctggctggtatct
gccgagggctcgcacccagagccagctcccttctgcgctgacaacccatcagagctgcca
ccttcaatagaacgcaccgggggcattggggactctcgacccccgtcctttcaccctcac
gctagtggaggcagccaggagaacctggacaatgacacggagaccgactccttggtgtct
gcccaacgagagcggccccgacggcgggacggcccagagcacgcagcccggctcaatgga
actgcaaagggggagcggcggcgggaacccggtggctacgacagttcatccacccttatg
agcagtgagctggagacgaccagcttctttgactcagatgaggatgactccaccagcagg
ttcagcagctccacagaacagagcagtgcctcgcgcctcatgaggagacacaagcggcgg
cggcggaagcagaaggtctcgcggatcgagcggtcttcgtccttcagcagcatcacggac
tccaccatgtcactcaatatcatcacagttactctcaacatggaaaagtataacttcttg
ggcatctccattgtgggccaaagcaacgagcgaggcgatggaggcatctacattggctcc
atcatgaagggtggggctgtggcagccgatggacgcatagaaccaggagatatgctgtta
caggtgaacgagatcaactttgagaacatgagtaacgatgacgccgtccgagtactccgg
gagattgtccacaagccagggcccatcactctgacggtagccaagtgctgggacccaagt
cctcgtgggtgcttcacattgccccggagtgagcctatccggcccattgaccctgcagcc
tgggtctctcacacagcagccatgacgggcaccttccctgcctatggcatgagcccctcc
ttgagcaccatcacctccaccagttcctccatcaccagctccattcccgacacagaacgc
ctagatgacttccacctctccatccacagtgacatggcggccatcgtaaaagccatggcc
tcccctgaatcagggttggaggttcgagaccgcatgtggctcaagattaccattcccaac
gctttcattggctcagatgtggtggactggctgtaccacaatgtggaaggattcacggac
cggcgggaggcccgcaagtatgccagcaacctgctgaaagctggtttcatccgccacacc
gtcaacaagatcacgttctctgagcagtgctactacatctttggtgacctctgtggcaat
atggccaacctgtcacttcacgaccatgacggctccagtggcgcctctgaccaggacaca
ctggctcctttgccgcacccgggggctgccccgtggcctatggctttcccttaccagtac
ccaccacctccgcatccctacaacccacaccccggcttcccagaactgggctacagctac
ggcggcggcgggggcagcgccagcagtcagcacagtgaaggcagtcgcagcagtggctcc
aaccgaagtggcagcgaccggcgcaaggagaaggacccaaaagctggggactccaaatca
ggcggtagcggcagcgaatcagaccacacgacccgcagcagtctgcgggggccgcgggag
cgggcgcccagcgagcgctcgggcccggcggccagcgaacacagccaccgcagcctgcgc
agccaccacacgcacccaagctacggcccgcccggagtgccccctctttatggccccccg
atgcttatgatgaccccgccgcctgcagccatggggcccccaggagcccctccaggccgt
gacctggcctcggtgcccccggaactgacggccagcagacagtccttccgcatggcaatg
ggaaaccccaccaagaatttcgggctctttgactttctgtga

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