KEGG   Oryctolagus cuniculus (rabbit): 100339336
Entry
100339336         CDS       T03373                                 
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X2
  KO
K02353  segment polarity protein dishevelled
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04150  mTOR signaling pathway
ocu04310  Wnt signaling pathway
ocu04330  Notch signaling pathway
ocu04390  Hippo signaling pathway
ocu04519  Cadherin signaling
ocu04550  Signaling pathways regulating pluripotency of stem cells
ocu04916  Melanogenesis
ocu04934  Cushing syndrome
ocu05010  Alzheimer disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05165  Human papillomavirus infection
ocu05200  Pathways in cancer
ocu05217  Basal cell carcinoma
ocu05224  Breast cancer
ocu05225  Hepatocellular carcinoma
ocu05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100339336
   04330 Notch signaling pathway
    100339336
   04390 Hippo signaling pathway
    100339336
   04150 mTOR signaling pathway
    100339336
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    100339336
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100339336
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100339336
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100339336
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100339336
   05226 Gastric cancer
    100339336
   05217 Basal cell carcinoma
    100339336
   05224 Breast cancer
    100339336
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100339336
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100339336
   05022 Pathways of neurodegeneration - multiple diseases
    100339336
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100339336
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100339336
NCBI-ProteinID: XP_008269029
Ensembl: ENSOCUG00000006978
LinkDB
Position
19:9525738..9533717
AA seq 736 aa
MAGSSTGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPETAPPAHEPRTELAPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERPRRRDSSEHGAGGHRPS
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRMERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGPSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEPGGTGDGGPPPSRGSTGGASNLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcagcacggggggcggaggcgtcggggagacgaaggtgatttaccacctg
gatgaggaggagactccctacctggtgaagatcccagtccccgccgagcgcatcaccctt
ggagacttcaagagcgttctgcagcggcccgcgggtgctaagtactttttcaagtccatg
gatcaggatttcggggtggtgaaggaagaaatttcagatgacaatgcccgcctgccctgc
ttcaacggaagggtggtatcctggctagtgtcgtcagataacccccagcctgagacggcc
cccccggcccacgagccgcggacagaactggcgcctccacccccacctttacctcctcta
cccccagagaggaccagtggcattggggactcaaggcctccatccttccaccctaatgtg
tccagcagccatgagaacctggagccagagacagaaacggagtccgtggtgtccctgagg
cgggagcggccccgccggagggacagcagcgagcatggcgctgggggccacaggcccagt
ggcccctcgaggctggaacgccacctggctgggtacgagagctcctccaccctcatgacc
agtgagctggagagtaccagcctgggggactcggatgaggacgacaccatgagcaggttc
agcagctccacggagcagagcagcgcctcccgcctcctcaagcgccaccggcggcggagg
aaacagcggcctccgcgcatggagaggacctcgtcctttagcagcgtcacggactccacc
atgtccctcaacatcatcacagtcacgctcaacatggagaagtacaacttcctgggaatc
tccattgtgggccaaagcaacgagcggggagacggaggcatctacatcggctccatcatg
aagggcggtgccgtggcggccgacgggcgcatcgagccgggggacatgctcttgcaggtg
aacgacatgaactttgagaacatgagcaacgatgatgccgtgcgggtgctgagggacatc
gtccacaagcccggccccatcgtgctgactgtggccaagtgttgggatccctctccccag
gcctatttcaccctcccccgaaatgaacccatccagccgattgaccctgccgcctgggtg
tcgcactctgccgcgctgactggcaccttcccagcctatcccggctcctcatccatgagc
accattacatccgggccctccctgcctgatggctgtgagggccggggtctctccatccac
acagacatggcatctgtgaccaaggccatggcagccccagagtccgggctggaagtccgc
gaccgcatgtggctcaagattaccatccccaatgcctttctgggctcggacgtggtcgac
tggctctaccatcacgtggagggcttccctgagcggcgggaggcgcgcaagtacgccagc
gggctgctcaaggcaggcctgatccggcacaccgtgaacaagatcaccttctctgagcag
tgctattacgtctttggtgacctcagtggcggctgtgagagttacctcgtcaacctgtct
ctgaatgacaacgatggctccagtggggcgtcagaccaggacaccctggctcctctgcct
ggggccaccccctggcccctgctgcccaccttctcctatcagtatccagccccacacccc
tacagcccccagcccccaccctaccacgagctttcgtcctacacctacggagggggcagt
gccagcagccagcacagtgaagggagccggagcagcgggtctacacgaagcgacgggggg
gctgggcgcacagggaggcctgaggagcgggcccccgagtccaagtccggcagtggcagt
gagtcggagccctccagcagggggggcagccttcgccggggcggggaacctggtgggact
ggcgatgggggtcctcccccgtccaggggctccacagggggtgcttccaatctcagagcc
cacccaggactccatccctacggaccaccccctggcatggccctcccgtataatcccatg
atggtggtcatgatgcccccgcccccaccccctgtccctccagcggtacagcccccaggg
gcccctccggtcagagacctgggttccgtacccccagaactgacagccagccgccagagc
ttccacatggccatgggcaaccccagcgagttctttgtggacgttatgtag

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