KEGG   Trachypithecus francoisi (Francois's langur): 117083812
Entry
117083812         CDS       T07225                                 
Symbol
DVL3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
tfn  Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150  mTOR signaling pathway
tfn04310  Wnt signaling pathway
tfn04330  Notch signaling pathway
tfn04390  Hippo signaling pathway
tfn04550  Signaling pathways regulating pluripotency of stem cells
tfn04916  Melanogenesis
tfn04934  Cushing syndrome
tfn05010  Alzheimer disease
tfn05022  Pathways of neurodegeneration - multiple diseases
tfn05165  Human papillomavirus infection
tfn05200  Pathways in cancer
tfn05217  Basal cell carcinoma
tfn05224  Breast cancer
tfn05225  Hepatocellular carcinoma
tfn05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:tfn00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    117083812 (DVL3)
   04330 Notch signaling pathway
    117083812 (DVL3)
   04390 Hippo signaling pathway
    117083812 (DVL3)
   04150 mTOR signaling pathway
    117083812 (DVL3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    117083812 (DVL3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    117083812 (DVL3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117083812 (DVL3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    117083812 (DVL3)
   05226 Gastric cancer
    117083812 (DVL3)
   05217 Basal cell carcinoma
    117083812 (DVL3)
   05224 Breast cancer
    117083812 (DVL3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    117083812 (DVL3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117083812 (DVL3)
   05022 Pathways of neurodegeneration - multiple diseases
    117083812 (DVL3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    117083812 (DVL3)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 117083812
NCBI-ProteinID: XP_033067758
LinkDB
Position
Unknown
AA seq 718 aa
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPDPAPFCADNPSELPPPMERTGGIGDSRPPSFHPH
AGGGSQENLDNDTETDSLVSAQRERPRRRDGPEHATRLNGTAKGERRREPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAA
WVSHTAAMTGTFPAYGMSPSLSTITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMA
SPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHT
VNKITFSEQCYYIFGDLCGNMANLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQY
PPPPHPYNPHPGFPELGYSYGGGSASSQHSEGSRSSGSNRSGSDRRKEKDPKAGDSKSGG
SGSESDHTTRSSLRGPRERAPSERSGPAASEHSHRSHHSLASSLRSHHTHPSYGPPGVPP
LYGPPMLMMPPPPAAMGPPGAPPGRDLASVPPELTASRQSFRMAMGNPTKNFGLFDFL
NT seq 2157 nt   +upstreamnt  +downstreamnt
atgggcgagaccaagatcatctaccacttggacgggcaggagacgccgtaccttgtgaag
ctacccctgcccgccgagcgcgtcacgttggcggactttaagggcgttttgcagcgaccc
agctataagttcttcttcaagtctatggacgacgatttcggagtggtgaaggaggagatc
tcggatgacaatgccaagctaccatgcttcaatggccgggtggtgtcctggctggtgtca
gctgagggctcacacccggacccagcccctttctgtgctgacaacccatcggagctgcca
ccacctatggagcgcacgggaggcatcggggactcccgacccccgtccttccaccctcat
gctggtgggggcagccaggagaacctggacaatgacacagagacggactccttggtgtct
gcccagcgagagcggccacgccggagggatggcccagagcatgcaactcggctaaatgga
actgcgaagggggagcggcggcgagaaccagggggttatgatagctcatccacccttatg
agcagcgagctggagaccaccagcttctttgactcagatgaggatgactccaccagcagg
ttcagcagctccacagaacagagcagcgcctcacgcctgatgagaagacacaaacggcgg
cggcggaagcagaaggtttctcggattgagcggtcctcgtccttcagcagcatcacggac
tccaccatgtcactcaacatcatcacggtcactctcaacatggaaaaatataacttcttg
ggcatctccattgtgggccaaagcaatgagcgtggtgacggcggcatctacattggctct
atcatgaagggtggggccgtggctgctgatggacgcatcgagccaggagatatgctgtta
caggtaaacgagatcaactttgagaacatgagtaatgacgatgcagtccgggtactgcgg
gagattgtgcacaaaccggggcccatcaccctgactgtagccaagtgctgggacccaagt
ccacgtggttgcttcacattgcccaggagcgagcccatccggcccattgaccctgcggcc
tgggtctcccacactgcagccatgaccggcaccttccctgcatacggcatgagcccctcc
ctgagcaccatcacctccaccagctcctccatcaccagttccatccctgacacagagcgc
ctagacgacttccacttgtccatccacagtgacatggctgccatcgtaaaagccatggcc
tcccctgaatcagggttggaggtccgtgaccgcatgtggctcaagattaccatccctaat
gctttcatcggctcagatgtagtggactggctgtaccacaatgtggaaggcttcacggac
cggagggaggcccgcaagtatgccagcaacctgctgaaagctggcttcatccgccatacc
gtcaacaagatcaccttctccgagcagtgctactacatcttcggcgacctctgcggcaac
atggccaacctgtctctccacgatcacgatggctccagtggcgcctctgaccaggacaca
ctggcccctttgccgcacccgggggccgccccttggcccatggctttcccgtaccagtac
ccgccacccccgcacccctacaacccgcacccgggcttcccggagctgggctacagctac
ggcgggggcagcgccagcagtcagcacagcgaaggcagtcggagcagtggctccaaccgt
agcggcagcgatcggaggaaggagaaagacccgaaggccggggactccaagtcggggggc
agcggcagcgaatcggaccacacgacacgcagcagcctgcgggggccgcgggagcgggcg
cccagcgagcgctcaggcccggcggccagcgagcacagccaccgcagccaccattcactt
gccagcagccttcgcagccaccacacacacccgagctacggtcctcctggagtgccccct
ctctacggcccccctatgctgatgatgcccccgccgcccgcggccatggggcccccagga
gcccctccgggccgcgacctggcctcagtgcccccggaactgaccgccagcagacagtcc
ttccgcatggccatgggaaaccccaccaagaatttcgggctgtttgactttctgtga

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