KEGG   Rhinopithecus roxellana (golden snub-nosed monkey): 104673334
Entry
104673334         CDS       T03989                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
rro  Rhinopithecus roxellana (golden snub-nosed monkey)
Pathway
rro04150  mTOR signaling pathway
rro04310  Wnt signaling pathway
rro04330  Notch signaling pathway
rro04390  Hippo signaling pathway
rro04550  Signaling pathways regulating pluripotency of stem cells
rro04916  Melanogenesis
rro04934  Cushing syndrome
rro05010  Alzheimer disease
rro05022  Pathways of neurodegeneration - multiple diseases
rro05165  Human papillomavirus infection
rro05200  Pathways in cancer
rro05217  Basal cell carcinoma
rro05224  Breast cancer
rro05225  Hepatocellular carcinoma
rro05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:rro00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    104673334 (DVL2)
   04330 Notch signaling pathway
    104673334 (DVL2)
   04390 Hippo signaling pathway
    104673334 (DVL2)
   04150 mTOR signaling pathway
    104673334 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    104673334 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    104673334 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    104673334 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    104673334 (DVL2)
   05226 Gastric cancer
    104673334 (DVL2)
   05217 Basal cell carcinoma
    104673334 (DVL2)
   05224 Breast cancer
    104673334 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    104673334 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104673334 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    104673334 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    104673334 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 104673334
NCBI-ProteinID: XP_010375635
UniProt: A0A2K6PSZ4
Position
19:complement(69450345..69459694)
AA seq 736 aa
MAGSSAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMAPPAHEPRAELAPPAPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERPRRRDSSEHGAGGHRTG
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEEDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMGNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTFGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEPSGTGDGGPPPSRGSTGGAPNLRT
HSGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcagcgctgggggcggtggggttggggagacgaaggtgatttaccacctg
gatgaggaagagactccatacctggtgaagatccctgttcccgccgagcgcatcaccctc
ggcgatttcaagagcgtcctgcagcggcccgcgggcgccaagtactttttcaagtctatg
gatcaggatttcggagtggtgaaagaagaaatttcagatgacaacgcccgcctcccctgc
ttcaacggaagggtggtatcctggctggtgtcctcagataatccccaacccgagatggct
cctccagcccacgagcctcgggcagaactggcgcctccagccccacctttaccccctttg
ccacccgagaggaccagcggcattggggactcaaggcctccatcctttcaccctaatgtg
tccagcagccatgagaatctggagcctgagacagaaaccgagtcagtagtgtcactgaga
cgggagcggcctcgcaggagagacagcagtgagcatggcgctgggggccacaggactggt
ggcccctcaaggctggagcgccacctggccggatatgagagctcctctaccctcatgacc
agtgagctggagagtaccagcctgggggactcggacgaggaggacaccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctccttaagcgccaccgacggcggagg
aagcagcggccaccccgcctggagaggacatcgtccttcagcagcgtcacagattccacc
atgtctctcaatatcatcacagtcacgctaaacatggagaagtacaacttcctgggtatc
tccattgtgggccaaagcaatgagcggggagacggaggcatctacattggctccatcatg
aagggtggggctgtggcagccgacgggcgcattgagccaggggacatgcttttgcaggtg
aatgacatgaacttcgagaacatgggcaatgacgacgccgtgcgggtgctgagggacatt
gtgcacaagcctggccccattgtgctgactgtggccaagtgctgggatccctctcctcag
gcctatttcactctccctcgaaatgagcccatccagccaattgaccctgctgcctgggtg
tcccactctgcggctctgactggcaccttcccagcctatccgggctcctcttccatgagc
accattacatctggatcctctttgcctgatggctgtgagggccggggtctttccatccat
acggacatggcatcggtgaccaaggccatggcagctccagagtctggactggaagtccgg
gaccgcatgtggctcaagatcaccatccctaatgcctttctgggctcggatgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgcaagtatgccagc
gggctgctcaaagcgggcctgatccgacacaccgtcaacaagatcaccttctctgagcag
tgctattacgtcttcggagacctcagtggtggctgtgagagctacctagtcaacctgtct
ctcaatgacaacgatggctccagtggggcttcggaccaggataccctggctcctctgccg
ggggccaccccctggcccttgctgcccactttctcctaccaatacccggccccacacccc
tacagcccgcagcccccaccctaccatgaactttcatcttatacctttggtgggggcagt
gccagcagccaacacagtgaaggcagccggagcagtgggtcgacacggagtgatgggggg
gcagggcgcacagggaggcccgaggagcgggcccccgagtccaagtccggcagtggcagt
gagtctgagccctccagccgagggggcagccttcggcggggtggggaaccaagtgggact
ggcgatgggggccctcctccatccagaggctcaactgggggtgcccctaatctccgaacc
cactcggggctccatccctatggaccaccccctggcatggccctcccctacaaccccatg
atggtggtcatgatgcccccacccccacctccagtccctccagcagtgcagcctccgggg
gcccctccagtcagagacctgggctctgtgccgccagaactgacagccagccgccaaagc
ttccacatggccatgggcaatcccagcgagttctttgtggatgttatgtag

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