KEGG   Phocoena phocoena (harbor porpoise): 136138000
Entry
136138000         CDS       T11058                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2
  KO
K02353  segment polarity protein dishevelled
Organism
pphc  Phocoena phocoena (harbor porpoise)
Pathway
pphc04150  mTOR signaling pathway
pphc04310  Wnt signaling pathway
pphc04330  Notch signaling pathway
pphc04390  Hippo signaling pathway
pphc04550  Signaling pathways regulating pluripotency of stem cells
pphc04916  Melanogenesis
pphc04934  Cushing syndrome
pphc05010  Alzheimer disease
pphc05022  Pathways of neurodegeneration - multiple diseases
pphc05165  Human papillomavirus infection
pphc05200  Pathways in cancer
pphc05217  Basal cell carcinoma
pphc05224  Breast cancer
pphc05225  Hepatocellular carcinoma
pphc05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pphc00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    136138000 (DVL2)
   04330 Notch signaling pathway
    136138000 (DVL2)
   04390 Hippo signaling pathway
    136138000 (DVL2)
   04150 mTOR signaling pathway
    136138000 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    136138000 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    136138000 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    136138000 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    136138000 (DVL2)
   05226 Gastric cancer
    136138000 (DVL2)
   05217 Basal cell carcinoma
    136138000 (DVL2)
   05224 Breast cancer
    136138000 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    136138000 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    136138000 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    136138000 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    136138000 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 136138000
NCBI-ProteinID: XP_065752525
LinkDB
Position
19:complement(50846888..50854351)
AA seq 735 aa
MAGSGAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSENPQPEMAPPAHEPRTDPVPPPPPVPPL
PPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVVSLRRERPRRRDSSERGAGGHRPS
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEEDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERASSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDDGSSGASDQDTLAPLPG
ATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGGV
GRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEPGGTGDGGPPPSRGSSGGAPNLRAH
PGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQSF
HMAMGNPSEFFVDVM
NT seq 2208 nt   +upstreamnt  +downstreamnt
atggcgggcagcggcgctgggggcggtggtgtcggggagacgaaggtgatttaccacctg
gatgaagaagagactccctacctggtgaagatccccgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgtcttgcagcggcccgcgggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagagatttcagatgacaatgctcgccttccctgc
ttcaacggaagggtggtatcctggttagtgtcatcagaaaacccccaacctgagatggcc
cccccagcccacgagcctcggacagacccggtgcctccaccgccacctgtaccccctctg
ccaccggagaggaccagtggcattggagactccaggcctccatccttccaccctaacgtg
tctagcagccgggaaaatctggagcccgagacagaaacagagtcagtggtgtctctgagg
cgggagcgacctcgcaggcgagacagcagtgagcgcggcgcggggggccaccgtcccagc
ggcccctcgaggctggagcgccacctggcagggtacgagagctcctccaccctcatgacc
agtgagctggagagcaccagcctgggggactcggatgaggaggacaccatgagcaggttc
agcagctccacggagcagagcagcgcctcccgcctcctcaagcgccaccggcggcggagg
aaacagcggccaccccgcctggagagggcctcatccttcagcagcgtcaccgattccacc
atgtctctcaacatcatcacagtcacgctcaacatggagaagtacaacttcctgggcatc
tccatcgtgggtcagagcaacgagcggggagatggaggcatctacatcggctccatcatg
aagggtggggctgtggcggctgatgggcgcattgagcccggggacatgcttttgcaggtg
aacgacatgaactttgagaacatgagcaacgatgatgcggtgcgggtgctgagggacatc
gtgcacaagccgggccccatcgtgctgactgtagccaagtgctgggatccctctccccag
gcctatttcactctcccccgaaatgagcccatccagccgattgaccctgctgcctgggtc
tcacactctgccgcgctgactggcaccttcccagcctatccaggctcttcgtccatgagc
accatcacctctgggtcctctcttccggatggctgtgagggccggggcctctccatccat
accgacatggcatctgtgaccaaggccatggcagctccagagtctggactggaagttcgg
gaccgcatgtggctcaagatcaccatccctaacgcctttctgggctcggacgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgaaagtatgccagc
gggctgctcaaggcaggccttatccggcacactgtgaacaagatcaccttctctgagcag
tgctattatgtctttggagacctcagtggcggctgtgagagttacctagtcaacctgtct
ctgaatgacgatggctccagtggcgcttcggaccaggacaccttggctcctttgcccggg
gccacgccctggcccctgctgcccaccttctcctaccagtacccagccccgcatccatac
agtccccagcccccaccctaccacgagctctcgtcctacacctacggcggaggcagtgcc
agcagccagcacagtgaggggagccggagcagtgggtcgacacgaagcgatgggggggtg
gggcgcacagggaggcctgaggagcgggcccctgagtccaagtctggcagcggcagtgag
tctgagccttccagccggggcggcagccttcggcggggcggggaacctggtgggactggt
gatgggggccctcccccatccaggggctcatcaggaggtgctcctaatctccgagcccac
ccagggctccatccctatggcccacctcctggcatggccctcccgtataaccccatgatg
gtggtcatgatgccccctcccccaccccctgtccctcctgcagtgcagcctccgggggcc
cctccagtcagagacctgggctccgtgcccccagagctgacggccagccgccaaagcttc
cacatggccatgggcaaccccagtgagttctttgtggatgttatgtag

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