KEGG   Cricetulus griseus (Chinese hamster): 100762587
Entry
100762587         CDS       T02813                                 
Symbol
Dvl2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X2
  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
    100762587 (Dvl2)
   04330 Notch signaling pathway
    100762587 (Dvl2)
   04390 Hippo signaling pathway
    100762587 (Dvl2)
   04150 mTOR signaling pathway
    100762587 (Dvl2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100762587 (Dvl2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100762587 (Dvl2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100762587 (Dvl2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100762587 (Dvl2)
   05226 Gastric cancer
    100762587 (Dvl2)
   05217 Basal cell carcinoma
    100762587 (Dvl2)
   05224 Breast cancer
    100762587 (Dvl2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100762587 (Dvl2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100762587 (Dvl2)
   05022 Pathways of neurodegeneration - multiple diseases
    100762587 (Dvl2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100762587 (Dvl2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100762587
NCBI-ProteinID: XP_027282762
UniProt: A0A8C2LIW3
LinkDB
Position
7:83848011..83857140
AA seq 736 aa
MAGSSAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMAPPAHESRTELVPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERTRRRDSSEHGAGGHRPS
GTSRLERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRMERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCESRGLSIH
MDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESELSSRGGSLRRGGEPSGTGDGGPPPSRGSTGGTPNLRA
LPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVSTAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcagcgcggggggcggtggtgtaggcgagacgaaggtgatttaccatctg
gatgaggaagagactccctacctggtgaagattcctgtcccggcggagcgcatcaccctc
ggcgatttcaagagcgttttgcagcggcccgcgggcgctaagtactttttcaagtctatg
gatcaggattttggggtggtgaaggaagagatttcagatgacaatgcccgcctaccttgc
ttcaatggaagggttgtctcctggctagtgtcatcagataacccccagcctgagatggct
cccccagcccatgagtctcggacagaactggttcctccacctccaccattaccgcctttg
cctccagaaagaaccagtggtattggggactcaagacctccatccttccaccccaatgtg
tccagcagccatgaaaatctagagcctgagacagaaactgagtctgttgtatcactgaga
cgagaacgaactcgaaggagagacagcagtgagcatggcgctggtggccacaggcccagt
ggcacctcaaggctggagcgccacctggctgggtacgagagttcttccaccctcatgacc
agtgagctggagagtaccagcctaggagactctgatgaggatgacaccatgagtagattc
agcagttccactgagcagagcagtgcctcccgcctcctcaagcgccaccgaaggcggaga
aagcagcggccaccacgcatggaaaggacctcatcctttagcagtgtcaccgattccaca
atgtctctcaacatcatcacagttacactcaacatggagaagtacaacttcctgggcatc
tccattgtgggccaaagtaatgagcggggtgacggaggcatctacatcggctccatcatg
aaggggggcgctgtggctgctgatgggcgcatagagcctggagacatgcttttgcaggtg
aatgatatgaactttgagaacatgagcaatgatgacgctgtacgggtactgagagacatt
gtgcacaaaccaggccccatcgtgctgaccgtggccaagtgctgggatccctctccccag
gcctacttcaccctcccccgaaatgagcccatccagccaattgatcccgctgcctgggtg
tcacactccgctgctctgactggcaccttccctgcttatccgggctcttcatctatgagc
actattacatctggctcgtccctgcctgatggctgtgaaagccggggtctctctatccac
atggacatggcctctgtgaccaaggccatggcagctccagaatctgggctagaagttcgg
gaccgcatgtggctcaagatcaccatcccaaatgcctttctaggctcagatgtggtagac
tggctgtaccatcatgtggaaggctttcctgagcgccgggaggcccggaagtatgccagt
ggactattgaaggcgggactcatccgacacactgtcaacaagattactttttctgagcag
tgctattatgtcttcggggacctcagtggtggctgtgaaagttacctagttaacctgtct
ctgaacgacaatgatggttccagtggggcttctgaccaggataccctggctcctcttcct
ggagctaccccctggcccctgctgcctaccttctcctaccagtacccagccccacaccca
tacagcccacagcctccaccctaccacgagctttcatcctatacttacggtggaggcagt
gccagcagccagcacagtgaagggagccggagcagtgggtcaacaagaagtgatgggggg
gccgggcgcacagggaggcctgaggaacgggcccctgagtcaaagtctggcagtggcagt
gagtccgagctttccagccggggaggcagccttcggcggggtggggaacccagtgggact
ggtgatgggggtccccctccatccaggggctcaacaggcggtactcctaatctccgagct
cttccagggctccatccctatggacctccccctggcatggctctcccctataatcccatg
atggtagtcatgatgcctccacccccaccccctgtctctactgcagtgcagccccctggt
gctcctccagttagagacctgggctctgtgcccccagaactgacagctagccgtcagagc
ttccacatggccatgggcaaccccagtgaattttttgtagatgttatgtag

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