KEGG   Galeopterus variegatus (Sunda flying lemur): 103593898
Entry
103593898         CDS       T08727                                 
Symbol
DVL3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
gvr  Galeopterus variegatus (Sunda flying lemur)
Pathway
gvr04150  mTOR signaling pathway
gvr04310  Wnt signaling pathway
gvr04330  Notch signaling pathway
gvr04390  Hippo signaling pathway
gvr04550  Signaling pathways regulating pluripotency of stem cells
gvr04916  Melanogenesis
gvr04934  Cushing syndrome
gvr05010  Alzheimer disease
gvr05022  Pathways of neurodegeneration - multiple diseases
gvr05165  Human papillomavirus infection
gvr05200  Pathways in cancer
gvr05217  Basal cell carcinoma
gvr05224  Breast cancer
gvr05225  Hepatocellular carcinoma
gvr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:gvr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103593898 (DVL3)
   04330 Notch signaling pathway
    103593898 (DVL3)
   04390 Hippo signaling pathway
    103593898 (DVL3)
   04150 mTOR signaling pathway
    103593898 (DVL3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103593898 (DVL3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103593898 (DVL3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103593898 (DVL3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103593898 (DVL3)
   05226 Gastric cancer
    103593898 (DVL3)
   05217 Basal cell carcinoma
    103593898 (DVL3)
   05224 Breast cancer
    103593898 (DVL3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103593898 (DVL3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103593898 (DVL3)
   05022 Pathways of neurodegeneration - multiple diseases
    103593898 (DVL3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103593898 (DVL3)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 103593898
NCBI-ProteinID: XP_008575211
UniProt: A0ABM0R3M0
LinkDB
Position
Unknown
AA seq 734 aa
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPEPAPFCADNPSELPPPMERTGGIGDSRPPSFHPH
AGGGSQENLDNDTETDSLVSAQRERPRRRDGPEHATRLNGTAKGERRREPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAA
WVSHTAAMTGTFPAYGMSPSLSTITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMA
SPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHT
VNKITFSEQCYYIFGDLCGNMANLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQY
PPPPHPYNPHPGFPELGYSYGGGSASSQHSEGSRSSGSNRSGSDRRKEKDPKAGDSKSGG
SGSESDHTTRSSLRGPRERAPSERSGPAASEHSHRSHHSLASSLRSHHTHPSYGPPGVPP
LYGPPMLMMPPPPAAMGPPGAPPGRDLASVPPELTASRQSFRMAMGNPRLPRILHLLGPD
LLVLPLTSVRPTHF
NT seq 2205 nt   +upstreamnt  +downstreamnt
atgggcgagaccaagatcatctaccacctggacgggcaggagacgccgtacctggtgaaa
ctgccgctgcccgccgagcgcgtcaccttggcggactttaagggcgttctgcagcgaccc
agctacaagttcttcttcaagtctatggacgacgacttcggagtggtgaaggaggagatc
tcagatgacaatgccaagctaccctgctttaacggccgggtggtgtcctggctagtgtca
gctgagggctcgcacccagagccagcccccttctgtgctgacaacccatcagagttgcca
ccgcctatggagcgcacaggaggcatcggggattcccgaccgccatccttccaccctcat
gctggtgggggcagccaggagaacctggacaatgacacagagacagactccttggtgtct
gcacagcgagagcggccacgccgaagggatggcccagagcatgcaacccggctaaatgga
actgcaaagggggagcggcggcgagagccagggggttatgatagctcatccacacttatg
agcagcgagctggagaccaccagcttctttgactcagatgaggatgactccaccagcagg
ttcagcagctccacagaacagagcagcgcctcacgcctgatgagaagacataagcggcgg
cggaggaagcagaaggtttctcggattgagcggtcctcgtccttcagcagcatcacggac
tccaccatgtcactcaacatcatcacagttactctcaacatggaaaagtataacttcttg
ggcatctccattgtcggccaaagcaatgaacgtggtgacggaggcatctacattggctct
atcatgaagggtggggccgtggctgctgatggacgcattgagccaggagatatgctgtta
caggtaaacgagatcaattttgagaacatgagtaatgacgatgcagtccgggtactgcgg
gagattgtgcacaaaccggggcccatcaccttgactgtagccaagtgctgggacccaagt
ccacgtggttgcttcacattgcccaggagcgagcccatccggcccattgaccctgcggcc
tgggtctcccacactgcggccatgacgggtaccttccctgcctacggcatgagcccctcc
ctgagcaccatcacctccaccagctcctccatcaccagctccatccctgacacagaacgc
ctagatgacttccacctgtccatccacagtgacatggccgctatagtaaaagctatggcc
tcccctgaatcagggctggaggttcgcgatcgcatgtggctcaagattaccatccccaac
gctttcatcggctcagacgtggtggactggttgtaccacaatgtggaaggcttcactgac
cggagggaggcccgcaagtatgccagcaacctgctgaaagctggctttatccgccacact
gtcaacaagatcaccttctctgagcagtgctactacatcttcggcgacctctgcggcaac
atggccaacttgtccctccatgaccacgacggctccagcggcgcctctgaccaggacacc
ctggctcctttgccgcacccaggagccgccccttggcccatggctttcccttaccagtac
ccaccacccccgcacccctacaacccacacccgggcttcccagagctgggctacagctac
ggtggaggcagtgccagcagtcagcacagtgaaggcagtcggagcagtggctccaaccgt
agcggcagcgatcggaggaaggagaaggacccaaaggccggggactccaagtcaggtggc
agcggcagtgagtcggaccacactacacgcagcagcctgcgggggccacgtgagcgggcg
cccagcgaacgctcgggcccagcagccagcgagcacagccaccgcagtcaccactcgctg
gccagcagcctgcgcagccaccacacacacccgagctacggccctccaggagtgccccct
ctctatggcccccccatgctgatgatgcccccacctcctgcggccatggggcccccagga
gcccctccgggccgcgacctggcctctgtgccccccgaactgaccgccagcagacagtcc
ttccgcatggccatgggaaaccccagacttcccaggatccttcacctcctgggaccggac
ttgctggtgctgccccttacttctgtccgccccacccacttttag

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