KEGG   Nannospalax galili (Upper Galilee mountains blind mole rat): 103752158
Entry
103752158         CDS       T03372                                 
Symbol
Dvl2
Name
(RefSeq) dishevelled segment polarity protein 2
  KO
K02353  segment polarity protein dishevelled
Organism
ngi  Nannospalax galili (Upper Galilee mountains blind mole rat)
Pathway
ngi04150  mTOR signaling pathway
ngi04310  Wnt signaling pathway
ngi04330  Notch signaling pathway
ngi04390  Hippo signaling pathway
ngi04550  Signaling pathways regulating pluripotency of stem cells
ngi04916  Melanogenesis
ngi04934  Cushing syndrome
ngi05010  Alzheimer disease
ngi05022  Pathways of neurodegeneration - multiple diseases
ngi05165  Human papillomavirus infection
ngi05200  Pathways in cancer
ngi05217  Basal cell carcinoma
ngi05224  Breast cancer
ngi05225  Hepatocellular carcinoma
ngi05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ngi00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103752158 (Dvl2)
   04330 Notch signaling pathway
    103752158 (Dvl2)
   04390 Hippo signaling pathway
    103752158 (Dvl2)
   04150 mTOR signaling pathway
    103752158 (Dvl2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103752158 (Dvl2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103752158 (Dvl2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103752158 (Dvl2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103752158 (Dvl2)
   05226 Gastric cancer
    103752158 (Dvl2)
   05217 Basal cell carcinoma
    103752158 (Dvl2)
   05224 Breast cancer
    103752158 (Dvl2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103752158 (Dvl2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103752158 (Dvl2)
   05022 Pathways of neurodegeneration - multiple diseases
    103752158 (Dvl2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103752158 (Dvl2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 103752158
NCBI-ProteinID: XP_008854073
LinkDB
Position
Un
AA seq 732 aa
MAGSSAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMALPAHEPRTELVPPPPPLPPL
PPERTSGIGDSRPPSFHHENLEPETETESVVSLRRERPRRRDSSEHGGGGHRPSGPSRLE
RHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRRKQRPPR
MERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVA
ADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQAYFTLP
RNEPIQPIDPAAWVSHSAALTGTFPTYPGSSSMSTITSGSSLPDGCEGRGLSIHMDMASV
TKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYASGLLKAG
LIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLPGATPWP
LLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGGAGRTGR
PEERAPESKSGSGSESELSSRGGSLRRGGEPSGTGDGGPPPSRGSTGGAPNLRALPGLHP
YGPPPGMALPYNPMMVVMMPPPPPPPPVPTAVQPPGAPPVRDLGSVPPELTASRQSFHMA
MGNPSEFFVDVM
NT seq 2199 nt   +upstreamnt  +downstreamnt
atggcgggcagcagtgcggggggcggtggtgtcggggagacgaaggtgatttaccacctg
gatgaggaggagactccctacctggtgaagatcccagtccccgcggagcgcatcaccctc
ggcgatttcaaaagcgttctgcagcggcccgccggcgctaagtactttttcaagtctatg
gatcaggattttggggtggtgaaggaagaaatttcagatgacaacgctcgcctgccttgt
ttcaatggaagggtagtctcctggctagtgtcatcggataatccccaacctgagatggca
ctcccagcccatgagcctcggacagaactggtgcctccacctccaccattacctcctttg
ccgccagaaaggaccagtggcattggggactcgaggcctccatccttccatcatgaaaat
ctggagcctgagacagaaactgagtctgttgtgtcactgagacgggagcgacctcgaagg
agagacagcagtgagcatggcggtggtggccacaggcccagtggcccttcaaggctggag
cgccacctggctgggtacgagagctcctctactctcatgactagtgagctggagagtacc
agcctaggggattcagatgaggatgacaccatgagtcggttcagcagctccacagagcag
agtagtgcctcccgcctcctcaagcgccaccgaaggcgaaggaagcaacgaccacctcgt
atggagaggacctcatccttcagcagcgtcacagattccacaatgtctctcaacatcatc
acagtcacactcaacatggagaagtacaactttctgggcatctccattgtgggccaaagt
aatgaacggggtgacggaggcatctacatcggctccatcatgaaagggggagctgtggct
gctgatggccgcatcgagcctggggacatgcttttgcaggtgaatgacatgaactttgag
aacatgagcaacgatgatgctgtgcgggttctgagagacattgttcacaaaccaggcccc
attgtgctgactgtggccaagtgttgggatccatcaccccaagcctacttcacccttccc
cgaaatgagcccatccagccaattgaccctgctgcctgggtgtcgcattctgctgcgctg
actggcaccttccctacttatccgggttcttcatccatgagcaccattacatctggatcc
tctctccctgatggctgtgaaggtcgaggtctctctatccatatggacatggcctctgtg
accaaagccatggcagccccagagtctgggctggaagtccgggaccgcatgtggctcaag
atcaccatcccaaatgcctttctaggctcagatgtggtcgactggctataccatcacgtg
gagggttttcctgagcgccgggaggcccgcaagtatgccagcgggctgttgaaggcaggc
cttatccgacacactgtgaacaagatcactttttctgagcagtgctattatgtcttcggg
gacctcagtggtggctgtgagagttacctagttaacctgtctttgaatgacaatgatggt
tccagtggggcttcagaccaggataccttggctcctttgcctggggctaccccctggccc
ctgctacccaccttttcctaccaatacccagccccgcacccctacagcccccaaccccca
ccctaccatgagctttcatcttacacctatggtggaggcagtgccagcagccagcacagt
gaggggagccggagcagtgggtcaacaagaagcgatgggggtgctgggcgcacagggagg
cccgaggaacgggctcctgagtcgaagtctggtagtggcagtgagtctgagctctctagc
cggggaggcagccttcggcggggtggggaacctagtgggactggtgatgggggtcctcct
ccatccaggggctcaacagggggtgctcccaatctccgagcccttccaggactccatccc
tatggacctccccctggtatggctctcccctataaccccatgatggtagtcatgatgcct
ccacccccacccccaccccctgtccctacagcagtgcagccccctggtgctcctccagtc
agggacctgggctctgtgcccccagaactgacagctagccgccagagcttccacatggct
atgggtaaccccagtgagttttttgtagatgttatgtaa

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