KEGG   Galeopterus variegatus (Sunda flying lemur): 103591440
Entry
103591440         CDS       T08727                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2
  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
    103591440 (DVL2)
   04330 Notch signaling pathway
    103591440 (DVL2)
   04390 Hippo signaling pathway
    103591440 (DVL2)
   04150 mTOR signaling pathway
    103591440 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103591440 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103591440 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103591440 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103591440 (DVL2)
   05226 Gastric cancer
    103591440 (DVL2)
   05217 Basal cell carcinoma
    103591440 (DVL2)
   05224 Breast cancer
    103591440 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103591440 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103591440 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    103591440 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103591440 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 103591440
NCBI-ProteinID: XP_008572113
UniProt: A0ABM0QUS2
LinkDB
Position
Unknown
AA seq 732 aa
MAGSSTGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEVAPPAHEPRTELAPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERPRRRDSTGGHRPSGPSR
LERHLAGYESSSTLMTSELESTSLGDSDEDDAMSRFSSSTEQSSASRLLKRHRRRRKQRP
PRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGA
VAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQAYFT
LPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCESRGLSIHTDMA
SVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYASGLLK
AGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLPGATP
WPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGGAGRT
GRPEERAPESKSGSGSESEPSSRGGSLRRGGEPGGIGEGGPPPSRGTTGGAPNLRAHPGL
HPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQSFHMA
MGNPSEFFVDVM
NT seq 2199 nt   +upstreamnt  +downstreamnt
atggcgggcagcagcaccgggggcggtggtgtcggggagacgaaggtgatttaccacctg
gatgaagaggagactccttacctggtgaagatccccgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgttctgcagcggcccgcaggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagaaatttcagatgacaatgcccgcctcccctgc
ttcaatggaagggtggtatcctggctagtgtcatcagataacccccagcctgaggtggct
cccccagcccatgagcctcggacggaactggcacctccacccccaccattaccccctttg
ccaccggagaggaccagtggcattggggactcaaggcctccctccttccaccctaatgtg
tccagcagccatgaaaatctggagcctgagacagaaaccgagtcagtagtgtccctgagg
cgggagcggcctcgcaggagagatagcactgggggccacagacccagtggcccctcaagg
ctggagcgccacctggctgggtacgagagctcctctactctcatgaccagtgagctggag
agtaccagcctgggggactcagatgaagacgatgccatgagcaggttcagcagctccaca
gagcagagcagcgcctcccgactcctcaagcgccaccggcggcggaggaaacagcggcca
ccccgcctggagaggacctcatccttcagcagcgtcacggattccacaatgtctctcaac
atcatcacagtcacactcaacatggagaagtacaacttcctgggcatctccattgtgggc
caaagcaatgagcggggagatggaggcatctacattggttccattatgaagggtggtgcc
gtggcagctgacgggcgcatcgagccaggggacatgcttttgcaggtgaatgacatgaac
tttgagaacatgagcaatgatgatgctgtgcgggtgctgagggacattgtgcacaagcct
ggccccattgtgctgactgtggccaagtgctgggatccctctccccaggcctatttcacc
ctcccccgaaatgagcccatccagccaattgaccctgctgcctgggtgtcacactctgct
gcgctgactggcaccttcccagcctatccaggctcctcgtccatgagcaccattacatct
ggatcctctctgcctgatggctgtgagagccgtggtctctccatccatactgacatggca
tctgtgaccaaggccatggcagctccagagtctgggctggaagtccgggaccgcatgtgg
cttaagatcaccatccctaatgcctttctgggctcagacgtggttgactggctctaccat
cacgtggagggctttcctgagcggcgggaagcccggaagtatgccagcgggctgctaaag
gcaggcttgatccgacacactgtgaacaagatcaccttctctgaacagtgctattatgtc
tttggagacctcagtggcggctgtgagagctacctagtcaacctgtccttgaatgacaac
gatggctccagtggggcttcagaccaggacaccctggctccactgcctggggccacccct
tggcccctgctgcctaccttctcctaccaatacccagccccacatccctacagcccccag
cccccaccctaccatgagctttcatcctatacctacggcgggggcagtgccagcagccag
cacagtgaggggagccggagcagtgggtcaacacgaagcgatgggggggcagggcgtaca
gggaggcctgaggagcgggcccctgagtccaagtctggcagtggcagtgagtctgagccc
tccagtcgagggggcagccttcggcggggcggggaacctggtgggattggcgaagggggc
cctccaccatccaggggcacaacagggggtgctcccaatctccgagcccatccaggactc
catccctatggaccaccccctggcatggcccttccctataaccccatgatggtggtcatg
atgcccccacccccaccccctgtccctccagcagtgcagcccccaggggcccctccagtc
agagacctgggctcagtgcccccagaactgacagccagccgccaaagcttccacatggcc
atgggcaacccgagtgagttctttgtagatgtaatgtag

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