KEGG   Eulemur rufifrons (Bennett's brown lemur): 138379591
Entry
138379591         CDS       T11398                                 
Symbol
DVL1
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-1 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
eruf  Eulemur rufifrons (Bennett's brown lemur)
Pathway
eruf04150  mTOR signaling pathway
eruf04310  Wnt signaling pathway
eruf04330  Notch signaling pathway
eruf04390  Hippo signaling pathway
eruf04550  Signaling pathways regulating pluripotency of stem cells
eruf04916  Melanogenesis
eruf04934  Cushing syndrome
eruf05010  Alzheimer disease
eruf05022  Pathways of neurodegeneration - multiple diseases
eruf05165  Human papillomavirus infection
eruf05200  Pathways in cancer
eruf05217  Basal cell carcinoma
eruf05224  Breast cancer
eruf05225  Hepatocellular carcinoma
eruf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:eruf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    138379591 (DVL1)
   04330 Notch signaling pathway
    138379591 (DVL1)
   04390 Hippo signaling pathway
    138379591 (DVL1)
   04150 mTOR signaling pathway
    138379591 (DVL1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    138379591 (DVL1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    138379591 (DVL1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    138379591 (DVL1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    138379591 (DVL1)
   05226 Gastric cancer
    138379591 (DVL1)
   05217 Basal cell carcinoma
    138379591 (DVL1)
   05224 Breast cancer
    138379591 (DVL1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    138379591 (DVL1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    138379591 (DVL1)
   05022 Pathways of neurodegeneration - multiple diseases
    138379591 (DVL1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    138379591 (DVL1)
SSDB
Other DBs
NCBI-GeneID: 138379591
NCBI-ProteinID: XP_069320793
LinkDB
Position
Unknown
AA seq 695 aa
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGVVK
EEIFDDNAKLPCFNGRVVSWLVLAEGAHSDAGSQGTDSHADLPPPLERTGGIGDSRPPSF
HPNVASSRDGMDNETGTESIVSHRRERARRRNREEAARTNGHPRGDRRRDLGLPPDSAST
LLSSELESSSFVDSDEDDDTSRLSSSTEQSTSSRLIRKHKRRRRKQRLRQTDRASSFSSI
TDSTMSLNIVTVTLNMERHHFLGISIVGQSNDRGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDVNFENMSNDDAVRVLREIVSQTGPISLTVAKCWDPTPRSYFTIPRADPVRPIDP
AAWLSHTAALTGALPRYGTSPCSSAVTRTSSSSLTSSVPGAPQLEDTPLTVKSDMGAVVR
VMQLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFRERREARKYASSMLKRGFL
RHTVNKITFSEQCYYVFGDLCSNLAALNLNSGSSGASDQDTLAPLPHPAAPWPLGQGYPY
QYPGPPPCFPPAYQDPGFSYGSGSTGSQQSEGSKSSGSTRSSRRPGREKECRAAGAGGSG
SESDHTAPSGVGGSGWRERPASQLSRGSSPRSQASATAPGLPPLHPLTKAYAVVGGPPGG
PPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq 2088 nt   +upstreamnt  +downstreamnt
atggcggagaccaagatcatctaccacatggacgaggaggagactccgtacctggtcaag
ctgcccgtggcccccgagcgcgtcacgctggccgacttcaagaacgtgctcagcaaccgg
cctgtgcacgcctacaaattcttcttcaagtccatggaccaggacttcggggtggtgaag
gaggagatcttcgacgacaacgccaagctgccctgcttcaacggccgtgtggtttcctgg
ctggtcttggccgagggtgctcactcggacgcgggctcccagggcactgacagccacgcg
gacctgcccccgcctctcgagcgcacgggtggcatcggagactcccggcccccctccttc
caccccaatgtggccagcagccgcgacgggatggacaatgagactggcacggagtccatc
gtcagccaccggcgggagcgagcccggcgccggaaccgcgaggaagccgcccggaccaat
gggcacccgaggggggaccggcggcgggacctggggctgcccccagacagcgcgtccacc
ctgctgagcagcgagctcgagtccagcagcttcgtcgactctgatgaggacgacgatacc
agcaggctgagcagctccacggagcagagcacctcttcccggctcatccggaagcacaag
cgccgccggcggaagcagcgcctgcggcagacggacagggcctcctccttcagcagcatc
actgactctaccatgtccctgaacatcgtcaccgtcacgctcaacatggagcggcaccac
ttcctgggcatcagcatcgtgggccagagcaacgaccggggtgatggtggcatctacatc
ggctccatcatgaagggcggggccgtggccgcggacggccgcatcgagccgggcgacatg
ctgctgcaggtgaacgacgtcaactttgagaacatgagcaacgacgacgcggtgcgggtg
ctgcgggagatcgtgtcccagacggggcccatcagcctcacggtggccaagtgctgggac
ccgactccccggagctacttcaccattccgagggccgacccagtgcggcccatcgacccg
gccgcctggctgtcccacacggcggcgctgacgggagccctgccgcgctacggtacgagc
ccttgctccagcgccgtgacgcgcaccagctcctcctcactaaccagctccgtgcctggc
gctccacagctggaggacaccccgctgacggtgaagagtgacatgggcgccgtcgtccgc
gtcatgcagctgccggattcgggactggagatccgcgaccgcatgtggctcaagatcacc
atcgccaatgccgtcatcggcgcggacgtggtggactggctgtacacgcacgtggagggc
ttccgggagcggcgggaggcgcggaagtacgccagcagcatgctgaagcgcggcttcctg
cggcacacggtcaacaagatcaccttctccgagcagtgctactacgtcttcggggacctg
tgcagcaatctcgcggccctgaacctcaacagtggctccagtggagcctccgaccaggac
acactggccccgctgccccacccggctgcaccctggcccctggggcagggctacccctac
cagtacccggggcccccaccctgcttcccacctgcctaccaggaccccggctttagctat
ggcagcggcagcaccgggagtcagcagagcgaagggagcaaaagcagcgggtccacccgg
agcagccggcgcccgggccgtgagaaggagtgccgggcagctggagccgggggcagcggc
agcgaatcggaccacacagcgccaagtggggtgggtggcagtggctggcgggagcgtccg
gccagccagctcagccgcggcagcagcccgcgcagtcaggcctcagccactgccccaggc
cttcccccgctgcaccccctgacgaaggcgtatgcagtggtgggggggccgccagggggg
ccccccgtccgggaactggccgctgtgcccccagagttgacaggcagccggcagtccttc
cagaaggccatggggaacccttgtgagttctttgtggacatcatgtga

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