KEGG   Odobenus rosmarus divergens (Pacific walrus): 101375453
Entry
101375453         CDS       T05148                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
oro  Odobenus rosmarus divergens (Pacific walrus)
Pathway
oro04150  mTOR signaling pathway
oro04310  Wnt signaling pathway
oro04330  Notch signaling pathway
oro04390  Hippo signaling pathway
oro04550  Signaling pathways regulating pluripotency of stem cells
oro04916  Melanogenesis
oro04934  Cushing syndrome
oro05010  Alzheimer disease
oro05022  Pathways of neurodegeneration - multiple diseases
oro05165  Human papillomavirus infection
oro05200  Pathways in cancer
oro05217  Basal cell carcinoma
oro05224  Breast cancer
oro05225  Hepatocellular carcinoma
oro05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:oro00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101375453 (DVL2)
   04330 Notch signaling pathway
    101375453 (DVL2)
   04390 Hippo signaling pathway
    101375453 (DVL2)
   04150 mTOR signaling pathway
    101375453 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101375453 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101375453 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101375453 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101375453 (DVL2)
   05226 Gastric cancer
    101375453 (DVL2)
   05217 Basal cell carcinoma
    101375453 (DVL2)
   05224 Breast cancer
    101375453 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101375453 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101375453 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    101375453 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101375453 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 101375453
NCBI-ProteinID: XP_004398597
UniProt: A0A2U3VTI9
LinkDB
Position
Unknown
AA seq 734 aa
MAGSGAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMAPPAHEPRTELAPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVVSVRRERPRRRDSSEHGAGGHRPS
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERASSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTMTSGSSLPEGCEGQGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVSLSLNDDGSSGASDQDTLAPLPG
ATPWPLLPAFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGGA
GRPGRPDERAPESKSGSGSESEPSSRGGSLRRGGDPGGADGGPPPSRGSAGGAPNLRAHP
GLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQSFH
MAMGNPSEFFVDVM
NT seq 2205 nt   +upstreamnt  +downstreamnt
atggcgggcagcggcgcggggggcggcggtgtcggggagaccaaggtgatataccatctg
gatgaagaagagactccctacctggtgaagatccccgttcccgccgagcgcatcactctc
ggcgatttcaagagcgtcctgcagcggcccgcgggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaggagatttcggatgacaacgcccgcctgccctgc
ttcaatggaagggtggtgtcctggctagtgtcatcagataacccccaacccgagatggct
cccccagcccacgagcctcggaccgaactggcgccaccgcccccaccgttacccccgttg
cccccagagaggaccagcggcattggggactctaggcctccgtccttccaccctaatgtg
tccagcagccgggaaaacctggagcctgagactgagacagagtcggtcgtgtcagtgcgg
cgggaacggcctcgcaggagagacagcagtgagcatggcgcggggggccacaggcccagt
ggcccgtcgaggctggagcgccacctggctgggtatgagagctcctcaaccctcatgacc
agcgagctggagagcaccagcctgggggactcagacgaggacgacaccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctcctcaagcgccaccggcggcggagg
aaacagcggccgccgcgcctggagagggcctcgtctttcagcagcgtcaccgactccacc
atgtctctcaacatcatcaccgtcacgctgaacatggagaagtacaacttcctgggcatc
tccatcgtgggccagagcaacgagcgtggtgacggcggcatctacatcggctccatcatg
aaggggggtgccgtggcggccgacgggcgcatcgagccgggcgacatgctgctgcaggtg
aacgacatgaacttcgagaacatgagcaacgacgacgcggtgcgcgtgctgcgggacatc
gtgcacaagccgggccccatcgtgctgacggtggccaagtgctgggatccctctccccag
gcctatttcactcttcctcgaaatgagcccatccagcccatcgaccctgctgcctgggtg
tcccactccgctgcgctgactggcaccttcccggcctatcccggctcttcgtccatgagc
accatgacgtcggggtcctctctgcctgagggctgtgaaggccagggtctttccatccac
acggacatggcatctgtgaccaaggccatggcagctccagagtctgggctggaagttcgg
gaccgcatgtggctcaagatcaccatccctaatgcctttctgggctcagacgtggttgac
tggctctaccatcacgtggaaggctttcccgagcggcgggaggcccgcaagtatgcgagt
gggctgctcaaggcgggcctcatccggcacaccgtgaacaagatcaccttctccgagcag
tgttactacgtcttcggggatctcagcggcggctgtgagagctacctcgtcagcctgtcc
ctgaatgacgacggctccagtggggcatcggaccaggacaccttggctcctctgcctggg
gccaccccctggcccctgctgcccgccttctcataccagtacccggccccgcacccgtac
agcccccagccgccgccctaccacgagctctcgtcctacacctacggaggtggcagtgcc
agcagccagcacagcgaggggagccggagcagtgggtcgacgcgaagcgatgggggggca
gggcgcccagggaggcctgacgagcgggcccccgagtccaagtccggcagcggcagtgag
tccgagccctccagccgcgggggcagcctccggcggggcggggatcccggcggggctgac
gggggccctcccccttccagaggctcggcaggcggtgctcccaatctccgagcccatcct
gggctccatccctacggaccgcccccggggatggccctcccctacaatcccatgatggtg
gtcatgatgcccccacctccaccccccgtccctccagccgtgcagcccccgggggcccct
ccggtcagagacctgggttctgtgcccccagagctgacagcaagccgccaaagtttccac
atggccatgggcaaccccagtgagttctttgtggatgttatgtag

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