KEGG   Cricetulus griseus (Chinese hamster): 100770288
Entry
100770288         CDS       T02813                                 
Symbol
Dvl1
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-1 isoform X4
  KO
K02353  segment polarity protein dishevelled
Organism
cge  Cricetulus griseus (Chinese hamster)
Pathway
cge04150  mTOR signaling pathway
cge04310  Wnt signaling pathway
cge04330  Notch signaling pathway
cge04390  Hippo signaling pathway
cge04550  Signaling pathways regulating pluripotency of stem cells
cge04916  Melanogenesis
cge04934  Cushing syndrome
cge05010  Alzheimer disease
cge05022  Pathways of neurodegeneration - multiple diseases
cge05165  Human papillomavirus infection
cge05200  Pathways in cancer
cge05217  Basal cell carcinoma
cge05224  Breast cancer
cge05225  Hepatocellular carcinoma
cge05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cge00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100770288 (Dvl1)
   04330 Notch signaling pathway
    100770288 (Dvl1)
   04390 Hippo signaling pathway
    100770288 (Dvl1)
   04150 mTOR signaling pathway
    100770288 (Dvl1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100770288 (Dvl1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100770288 (Dvl1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100770288 (Dvl1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100770288 (Dvl1)
   05226 Gastric cancer
    100770288 (Dvl1)
   05217 Basal cell carcinoma
    100770288 (Dvl1)
   05224 Breast cancer
    100770288 (Dvl1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100770288 (Dvl1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100770288 (Dvl1)
   05022 Pathways of neurodegeneration - multiple diseases
    100770288 (Dvl1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100770288 (Dvl1)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX PDZ DEP PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100770288
NCBI-ProteinID: XP_027254385
UniProt: G3I423
LinkDB
Position
2:complement(425743..437819)
AA seq 695 aa
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGVVK
EEIFDDNAKLPCFNGRVVSWLVLAEGAHSDAGSQGTDSHTDLPPPLERTGGIGDSRPPSF
HPNVASSRDGMDNETGTESMVSHRRERARRRNRDEASRTNGHPRGDRRRDLGLPPDSAST
VLSSELESSSFIDSDEEDNTSRLSSSTEQSTSSRLIRKHKCRRRKQRLRQTDRASSFSSI
TDSTMSLNIITVTLNMERHHFLGISIVGQSNDRGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDVNFENMSNDDAVRVLREIVSQTGPISLTVAKCWDPTPRSYFTIPRADPVRPIDP
AAWLSHTAALTGALPRYGTSPCSSAITRTSSSSLTSSVPGAPQLEEAPLTVKSDMSAIVR
VMQLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFRERREARKYASSMLKRGFL
RHTVNKITFSEQCYYVFGDLCTNLASLNLNSGSSGASDQDTLAPLPHPSVPWPLGQGYPY
QYPGPPPCFPPAYQDPGFSYGSGSAGSQQSEGSKSSGSTRSSHRTPGREERRAAGAGGSG
SESDHTAPSGSGSTGWWERPVSQLSHGSSPRSQASAVAPGLPPLHPLTKAYAVVGGPPGG
PPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq 2088 nt   +upstreamnt  +downstreamnt
atggcggagaccaagatcatctaccacatggacgaggaggagacgccgtacctggtcaag
ctgccggtagctcccgaacgcgtcacgctggcggacttcaagaacgtgctcagcaaccgg
ccggtgcacgcctacaaattcttcttcaagtctatggaccaggacttcggggtggtgaag
gaggagatcttcgatgacaatgccaagttgccctgcttcaatggccgggtggtttcctgg
ctggtcctggctgagggcgctcactcggacgcagggtcccagggcactgacagccacacg
gacctgcccccaccccttgagaggacaggcggcattggggactccaggcccccctccttc
catccaaatgttgccagtagccgtgatggaatggacaatgagacaggcacagagtccatg
gtcagtcaccggcgggagcgagcccgacgtcgaaaccgtgatgaggcttcccggaccaat
gggcacccgaggggagaccggcgacgggatctgggactgcctccagacagtgcatccact
gtgttgagcagtgagcttgaatctagcagctttattgactcagatgaggaggataacaca
agccggctgagcagttctacagagcagagcacctcctctcggctaattcgtaagcacaaa
tgtcgtcgtcggaagcagcgcttgaggcagacagaccgggcatcctccttcagcagcatc
accgactccaccatgtccctgaacatcatcaccgtcactctcaacatggagaggcaccac
ttcctgggcatcagcatcgtgggccagagcaacgaccggggtgatggcggcatctacatt
ggatccatcatgaagggcggagctgtggctgctgatggccgcattgagccaggcgacatg
ctgctgcaggtcaatgatgtcaactttgagaacatgagcaacgatgacgctgtgcgggtg
cttcgggagatcgtatcccaaacggggcccatcagcctcacagtggccaagtgctgggac
ccaacccctcggagctactttaccatcccaagggctgacccagtgcgacccatcgacccg
gctgcctggctgtcccacacagcagcgctgacgggtgctctgccccgctatggtacgagt
ccctgctccagtgccatcacacgcaccagctcttcctcactaaccagctcagtgcctggc
gccccacagcttgaggaggcaccactgacagtgaagagtgacatgagcgccattgtccgg
gtcatgcagttgccagactcaggactggagattcgggaccgcatgtggcttaagatcacc
attgccaatgctgtcattggggcggatgtggtggactggctgtacacgcatgtggagggc
ttcagagagcgaagagaggcgaggaagtatgccagcagtatgctgaagcgcggcttcttg
aggcacaccgtcaacaagatcaccttctctgagcagtgctactatgtctttggggacctg
tgcactaaccttgcatccctgaacctcaacagtggctccagtggagcctcagatcaggac
acactggcccccctgccccacccatctgtaccctggcccttgggtcaaggctacccctac
cagtacccagggcccccgccctgcttcccacctgcttaccaggaccctggcttcagctat
ggcagtggcagtgctgggagtcagcagagtgaagggagcaagagcagtgggtccacaagg
agcagccatcggaccccaggccgagaggagcgccgggcagctggagctgggggcagtggc
agcgaatcagatcacacggcaccaagtgggtctggtagcactggctggtgggagcgtcca
gtcagccagcttagccatggcagtagccctagaagtcaggcgtcagctgttgccccaggt
ctccccccactgcaccccctgacaaaggcctatgcagtagtgggtgggccacctggaggg
ccacctgtccgggagctggctgctgttcctccggaacttacaggtagccgccagtccttc
caaaaggctatgggaaatccctgtgagttctttgtggacattatgtga

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