KEGG   Gracilinanus agilis (agile gracile opossum): 123244708
Entry
123244708         CDS       T07702                                 
Symbol
DVL3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
gas  Gracilinanus agilis (agile gracile opossum)
Pathway
gas04150  mTOR signaling pathway
gas04310  Wnt signaling pathway
gas04330  Notch signaling pathway
gas04390  Hippo signaling pathway
gas04550  Signaling pathways regulating pluripotency of stem cells
gas04916  Melanogenesis
gas04934  Cushing syndrome
gas05010  Alzheimer disease
gas05022  Pathways of neurodegeneration - multiple diseases
gas05165  Human papillomavirus infection
gas05200  Pathways in cancer
gas05217  Basal cell carcinoma
gas05224  Breast cancer
gas05225  Hepatocellular carcinoma
gas05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:gas00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    123244708 (DVL3)
   04330 Notch signaling pathway
    123244708 (DVL3)
   04390 Hippo signaling pathway
    123244708 (DVL3)
   04150 mTOR signaling pathway
    123244708 (DVL3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    123244708 (DVL3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    123244708 (DVL3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    123244708 (DVL3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    123244708 (DVL3)
   05226 Gastric cancer
    123244708 (DVL3)
   05217 Basal cell carcinoma
    123244708 (DVL3)
   05224 Breast cancer
    123244708 (DVL3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    123244708 (DVL3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    123244708 (DVL3)
   05022 Pathways of neurodegeneration - multiple diseases
    123244708 (DVL3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    123244708 (DVL3)
SSDB
Motif
Pfam: Dsh_C Dishevelled DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 123244708
NCBI-ProteinID: XP_044529191
LinkDB
Position
4:complement(509169852..509192879)
AA seq 732 aa
MTTRGSRVSMAGWCPGWCRPRARTLSQAPSAPTTPPSCHPPWNAPAASGTRGLPPSRAAP
AEGWAGAWRCVPPHPDPGPLPVPLTGPWRPPRGHGSPQRPQVPPAGWQWQVQTGVLRFHS
PHHTPLPLPGPPGLESGPPLVCPAPRPLPSPAPSSTVSRINGTAKGERRREPGGYDSSST
LMSSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVARIERSSSFSSI
TDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSKWMGESAL
KLVPGTCEPIRPIDPAAWVSHTAAMTGTFPAYGMSPSLSTITSTSSSIASSIPDTERLDD
FHLSIHSDMATIVKAMASPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRRE
ARKYASNLLKAGFIRHTVNKITFSEQCYYIFGDLCGNMANLSLHDQDGSSGASDQDTLAP
LPHPGAAPWPMAFPYQYPPPPHPYNPHPGFPEPGYSYGGGGSAGSQHSEGSRSSGSNRSG
SDRRKEKDPKAGDSKSGGSGSESDHTSRSSLRRERAPSERSGPAASEHSVRSHHSLAHSL
RSHHTHQSYGPPGVPPLYGPPMLMMPPPPAAMGPPGAPPGRDLASVPPELTASRQSFRMA
MGNPSEFFVDVM
NT seq 2199 nt   +upstreamnt  +downstreamnt
atgacaacgcgaggctcccgtgtttcaatggccgggtggtgtcctggctggtgtcggccg
agggctcgcaccctgagccaggctccttctgccccgacaacccctccgagctgccacccc
ccatggaacgcaccggcggcatcggggactcgcggcctccctccttccagagcggccccg
gcggagggatgggccggagcatggcggtgcgtaccccctcaccctgaccccggccccctg
cccgtcccactgactggaccctggcggccccccagaggccacgggtccccccagaggccg
caggtccccccggcaggctggcagtggcaggtccagacgggggtcctcagattccattct
ccccatcacaccccactacctctcccgggcccgcctggcctggaatctgggccccccttg
gtgtgcccggccccccggcctctcccatcccctgccccctcctccacagtgtcccggata
aacggtacggccaaaggggagcggaggagggagcccgggggctacgacagctcttccacc
ctcatgagcagcgagctggaaaccacgagcttcttcgactccgacgaggatgattcgacc
agcaggttcagcagctccacagagcagagcagcgcctcccgcctcatgaggagacacaag
cggcgccggcggaagcagaaagtggcccggatcgagcggtcctcatccttcagcagcatc
acggattccaccatgtccctcaacatcatcaccgtcacgctcaacatggagaaatacaac
ttcctgggcatctccattgtgggtcagagcaacgaacggggtgatgggggcatctacatt
ggctccatcatgaagggtggcgccgtggccgctgatgggcggatcgagccgggggacatg
ctcctacaggtaaacgacatcaattttgagaatatgagtaatgacgacgctgtccgggtg
ctccgggaaatcgtgcacaaaccagggcccatcaccttgacagtggccaagtgctgggac
cccagccccagaggctgcttcaccctgcccaggagtaagtggatgggggagtcggcccta
aagctggtgcctggcacatgtgagccaatccgacccattgaccctgcggcctgggtgtcc
cacacagcagcaatgacaggcaccttccctgcctatggcatgagcccctccctcagtacc
atcacctctactagctcttccatcgccagctccattcctgacactgaacgcctcgatgac
tttcacctgtccatccacagcgacatggccaccatagtcaaagctatggcttcacctgag
tctgggctggaggtccgagaccgaatgtggctcaaaatcaccatccccaacgctttcatc
ggttcagatgtagtggactggctgtaccacaacgtggaaggcttcacagaccggcgagag
gcccggaaatacgccagcaacctactgaaagccggtttcatccgacacacagtcaacaag
atcaccttctcagaacagtgctattatatctttggtgacctctgtggcaacatggctaac
ttgtccctgcacgaccaggacggctccagtggggcctcggaccaagacacgctggctcct
ctccctcaccccggagctgccccgtggcccatggccttcccttatcagtacccacccccc
ccacatccctataatcctcaccccggcttccccgagcccgggtacagctacggcggcggg
gggagtgcgggcagccagcacagtgaaggcagccggagcagcggctccaaccgcagcggc
agcgaccggcggaaggagaaggacccaaaggccggggactccaagtcagggggcagcgga
agcgagtcggaccacacgagccgaagcagcctgaggcgggagagagcccccagcgaacgc
tcaggcccagccgccagcgagcacagcgtccgcagccaccactcgctggcccacagcctc
cgcagccaccacacacaccagtcctatgggcccccgggggtgcccccgctgtacggcccg
cccatgctgatgatgccccctccacccgctgccatgggccccccgggcgcccccccgggc
cgagacctggcctcggtgcccccagaactgaccgccagcagacagtccttccgcatggcc
atgggaaaccccagtgagttctttgtggatgtgatgtga

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