KEGG   Cricetulus griseus (Chinese hamster): 100773535
Entry
100773535         CDS       T02813                                 
Symbol
Dvl3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X2
  KO
K02353  segment polarity protein dishevelled
Organism
cge  Cricetulus griseus (Chinese hamster)
Pathway
cge04150  mTOR signaling pathway
cge04310  Wnt signaling pathway
cge04330  Notch signaling pathway
cge04390  Hippo signaling pathway
cge04550  Signaling pathways regulating pluripotency of stem cells
cge04916  Melanogenesis
cge04934  Cushing syndrome
cge05010  Alzheimer disease
cge05022  Pathways of neurodegeneration - multiple diseases
cge05165  Human papillomavirus infection
cge05200  Pathways in cancer
cge05217  Basal cell carcinoma
cge05224  Breast cancer
cge05225  Hepatocellular carcinoma
cge05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cge00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100773535 (Dvl3)
   04330 Notch signaling pathway
    100773535 (Dvl3)
   04390 Hippo signaling pathway
    100773535 (Dvl3)
   04150 mTOR signaling pathway
    100773535 (Dvl3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100773535 (Dvl3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100773535 (Dvl3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100773535 (Dvl3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100773535 (Dvl3)
   05226 Gastric cancer
    100773535 (Dvl3)
   05217 Basal cell carcinoma
    100773535 (Dvl3)
   05224 Breast cancer
    100773535 (Dvl3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100773535 (Dvl3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100773535 (Dvl3)
   05022 Pathways of neurodegeneration - multiple diseases
    100773535 (Dvl3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100773535 (Dvl3)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100773535
NCBI-ProteinID: XP_027268865
UniProt: A0A9J7FVC0
Position
4:complement(68104597..68120096)
AA seq 716 aa
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPEPAPFCADNPSELPPSMERTGGIGDSRPPSFHPH
ASGGSQENLDNDTETDSLVSAQRERPRRRDGPEHAARLNGTAKGERRREPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAA
WVSHTAAMTGTFPAYGMSPSLSTITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMA
SPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHT
VNKITFSEQCYYIFGDLCGNMANLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQY
PPPPHPYNPHPGFPELGYSYGGGSASSQHSEGSRSSGSNRSGSDRRKEKDPKAGDSKSGG
SGSESDHTTRSSLRGPRERAPSERSGPAASEHSHRSHHSLTSSLRSHHTHPSYGPPGVPP
LYGPPMLMMTPPPAAMGPPGAPPGRDLASVPPELTASRQSFRMAMGNPSEFFVDVM
NT seq 2151 nt   +upstreamnt  +downstreamnt
atgggcgagaccaagatcatctaccacctggacggccaggagacgccgtacctggtgaag
ctgcccctgcccgccgagcgcgtcaccttggcggactttaagggcgttctgcagcggccc
agctataagttcttcttcaagtctatggacgacgattttggagtggtgaaggaagagatc
tcagacgacaatgccaagctgccctgcttcaatggtcgggtggtgtcctggctggtatct
gctgagggttcccacccagagccagccccattctgtgccgacaacccatcagagctgcca
ccttcaatggagcgcacaggaggcattggggactctcgacccccatcctttcaccctcat
gctagtggaggcagccaagaaaacctggacaatgacacggagactgactccttggtgtct
gcccaacgagagcgtccccgtcggagggatggcccagagcacgcagcccggctcaatgga
actgcgaagggggagcggaggcgagagccaggtggctatgacagttcatctacccttatg
agcagtgagctggagactaccagcttctttgactcagatgaggacgactccaccagcagg
ttcagcagctccacagaacagagcagtgcctcgcgcctaatgaggagacacaagcggcgg
cggcggaagcagaaggtctctcggattgagcggtcttcgtccttcagcagcatcacagac
tccactatgtctctcaatatcatcacagttactctcaacatggaaaagtataacttcttg
ggcatctccattgtgggccaaagcaacgagcgaggtgatggaggcatctacattggctcc
atcatgaagggtggggctgtggcagccgatggacgcattgaaccaggagatatgctgtta
caggtgaatgagatcaactttgagaacatgagtaatgacgatgccgtccgagtacttcgg
gagattgtacacaaaccagggcccatcactctgactgtagccaagtgctgggacccaagt
ccacgtggctgcttcacattaccgcggagtgagcccatccggcccatcgacccagcagcc
tgggtctctcacactgcagccatgacaggcaccttccctgcctatggcatgagcccctcc
ctgagtaccatcacctccactagctcctccatcaccagctccatccctgacacagaacgc
ctagatgacttccacctctccatccacagtgacatggcagccatcgtaaaagccatggcc
tcccctgaatcagggttggaggttcgagaccgcatgtggctcaagattaccattcccaat
gctttcattggctcagatgtggtggactggctgtaccacaacgtggaaggattcacggac
cggcgggaggcccggaagtacgccagcaacctgctgaaagctggtttcatccgccatact
gtcaacaaaatcaccttctctgaacagtgctactatatctttggtgacctctgtggcaac
atggccaacctgtcacttcacgaccatgatggctccagcggcgcctctgaccaggacacc
ctggctcctttgccgcacccaggggctgccccttggcctatggctttcccttaccagtac
ccaccacctccgcatccctacaatccacacccaggcttcccagaactgggctacagctac
ggtgggggtagcgccagcagtcaacacagtgaaggcagtcgaagcagtggctccaacaga
agtggcagcgaccggcgcaaggagaaggacccaaaagctggggactccaaatcaggtggt
agtggcagcgagtcagaccacactacacgcagcagtctgagaggtccacgggagcgggcg
ccaagtgagcgctcaggcccagcagccagcgagcacagtcaccgcagccaccattcgctg
accagcagcctgcgcagccaccacacacacccgagctatggcccgcccggagtgccccct
ctatatggtcccccgatgcttatgatgaccccaccacctgcagccatggggcccccagga
gcccctccaggccgtgacctggcctcggtgcccccggaactgacggccagcagacagtcc
ttccgcatggcaatgggaaaccccagtgagttctttgtggatgtgatgtga

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