KEGG   Microcebus murinus (gray mouse lemur): 105855775
Entry
105855775         CDS       T07238                                 
Symbol
DVL3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
mmur  Microcebus murinus (gray mouse lemur)
Pathway
mmur04150  mTOR signaling pathway
mmur04310  Wnt signaling pathway
mmur04330  Notch signaling pathway
mmur04390  Hippo signaling pathway
mmur04550  Signaling pathways regulating pluripotency of stem cells
mmur04916  Melanogenesis
mmur04934  Cushing syndrome
mmur05010  Alzheimer disease
mmur05022  Pathways of neurodegeneration - multiple diseases
mmur05165  Human papillomavirus infection
mmur05200  Pathways in cancer
mmur05217  Basal cell carcinoma
mmur05224  Breast cancer
mmur05225  Hepatocellular carcinoma
mmur05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mmur00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105855775 (DVL3)
   04330 Notch signaling pathway
    105855775 (DVL3)
   04390 Hippo signaling pathway
    105855775 (DVL3)
   04150 mTOR signaling pathway
    105855775 (DVL3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105855775 (DVL3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105855775 (DVL3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105855775 (DVL3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105855775 (DVL3)
   05226 Gastric cancer
    105855775 (DVL3)
   05217 Basal cell carcinoma
    105855775 (DVL3)
   05224 Breast cancer
    105855775 (DVL3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105855775 (DVL3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105855775 (DVL3)
   05022 Pathways of neurodegeneration - multiple diseases
    105855775 (DVL3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105855775 (DVL3)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 105855775
NCBI-ProteinID: XP_012592380
Ensembl: ENSMICG00000049000
UniProt: A0A8B7EFY4
LinkDB
Position
1:76709765..76726044
AA seq 718 aa
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPEPAPFCADNPSELPPPMERTGGIGDSRPPSFHPH
ACGGSQENLDNDTETDSLVSAQRERPRRRDGPDHAARLNGTAKGERRREPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAA
WVSHTAAMTGTFPAYGMSPSLSTITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMA
SPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHT
VNKITFSEQCYYIFGDLCGNMANLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQY
PPPPHPYNPHPGFPELGYSYGGGSASSQHSEGSRSSGSNRSGSDRRKEKDAKTGDSKSGG
SGSESDHTTRSSLRGPRERAPSERSGPAASEHSHRSHHSLASSLRSHHTHPSYGPPGVPP
LYGPPMLMMPPPPAALGPPGAPPGRDLASVPPELTASRQSFRMAMGNPTKNFGLFDFL
NT seq 2157 nt   +upstreamnt  +downstreamnt
atgggcgagaccaagatcatctaccacctggacgggcaggagacgccgtacctggtgaag
ctgcccctgcccgccgagcgcgtcaccctggcggactttaagggcgttctgcagcgaccc
agctataagttcttcttcaagtctatggacgacgatttcggagtggtgaaggaggagatc
tcagacgacaatgccaagttaccctgcttcaatggccgggtggtgtcctggctggtatca
gctgagggctcacacccagagccagcccctttctgtgctgacaacccatctgagctgccg
ccacctatggagcgcacaggaggcatcggggactcccgacccccatccttccaccctcat
gcttgtgggggaagccaggagaacttggacaatgacacagagacggactccttggtgtct
gcccagcgggagcggccacgtcggagggatggcccagaccatgcggctcggctaaatgga
actgcgaaaggggagcggcggcgagagccaggcggttatgatagctcatccacccttatg
agcagcgagttggagaccaccagcttctttgactcagatgaagatgactccaccagcagg
ttcagcagctccacagaacagagcagtgcctcacgcctgatgagaagacacaagcggcgc
aggcggaaacagaaggtttctcggatcgagcggtcctcatccttcagcagcatcacggac
tccaccatgtcactcaacatcatcacagttactctcaacatggaaaagtataacttcttg
ggcatctccattgtgggccaaagcaacgagcgtggtgacggtggcatctacattggctct
atcatgaagggtggggccgtggctgctgatggacgcatcgagccaggagacatgctgtta
caggtaaatgagatcaactttgagaacatgagtaacgacgatgcagtccgggtactgcgg
gagattgtgcacaaaccgggacctatcaccctgactgtagccaagtgctgggacccaagt
ccacgtggttgcttcacattgcccaggagcgagcccatccggcccattgatcctgcggcc
tgggtctcccacactgcagccatgacgggcaccttccctgcctacggcatgagcccctcc
ctgagcaccatcacctccaccagctcctccatcaccagttccatccctgacacagagcgc
ctagacgacttccacctatccatccacagtgacatggccgccatcgtaaaagccatggcc
tcccctgaatcagggttggaggtccgcgaccgcatgtggctcaagattaccatccctaac
gctttcatcggctcagatgtggtggactggctgtaccacaacgtggaaggcttcactgac
cggagggaggcccgcaagtatgccagcaacctactaaaagctggcttcatccgccacact
gtcaacaagatcaccttctctgagcagtgctactacatcttcggcgacctctgcggcaac
atggccaacctctccctccacgaccatgatggctccagtggcgcctctgaccaggacacg
ctggcccctttgccgcaccctggggccgccccttggcccatggcttttccttaccagtac
ccgccgcccccgcacccttacaacccacacccgggcttcccggagctgggctacagctac
ggcggtggcagtgccagcagtcagcacagtgaaggcagtcggagcagtggctccaaccgc
agtggcagcgatcggaggaaggagaaggatgcgaagactggggactccaagtccgggggc
agcggcagtgaatcggaccacacgacacgcagcagcctgcgggggccacgggaacgggcg
ccaagtgagcgctcaggcccagcggccagcgagcacagccaccgcagccaccactcactg
gccagcagcctgcgcagccaccacacacacccaagctacggccctcccggagtgccccct
ctttacggcccccccatgctgatgatgcccccaccacccgcggccctgggacccccagga
gcccctccgggccgcgacctggcctccgtgcccccggaactgaccgccagcagacagtcc
ttccgcatggccatgggaaaccccaccaagaatttcgggctgtttgactttctgtga

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