KEGG   Physeter macrocephalus (sperm whale): 102980874
Entry
102980874         CDS       T06011                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X4
  KO
K02353  segment polarity protein dishevelled
Organism
pcad  Physeter macrocephalus (sperm whale)
Pathway
pcad04150  mTOR signaling pathway
pcad04310  Wnt signaling pathway
pcad04330  Notch signaling pathway
pcad04390  Hippo signaling pathway
pcad04550  Signaling pathways regulating pluripotency of stem cells
pcad04916  Melanogenesis
pcad04934  Cushing syndrome
pcad05010  Alzheimer disease
pcad05022  Pathways of neurodegeneration - multiple diseases
pcad05165  Human papillomavirus infection
pcad05200  Pathways in cancer
pcad05217  Basal cell carcinoma
pcad05224  Breast cancer
pcad05225  Hepatocellular carcinoma
pcad05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pcad00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102980874 (DVL2)
   04330 Notch signaling pathway
    102980874 (DVL2)
   04390 Hippo signaling pathway
    102980874 (DVL2)
   04150 mTOR signaling pathway
    102980874 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102980874 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102980874 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102980874 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102980874 (DVL2)
   05226 Gastric cancer
    102980874 (DVL2)
   05217 Basal cell carcinoma
    102980874 (DVL2)
   05224 Breast cancer
    102980874 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102980874 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102980874 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    102980874 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102980874 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 102980874
NCBI-ProteinID: XP_007100771
Ensembl: ENSPCTG00005014347
UniProt: A0A2Y9EF70
LinkDB
Position
Unknown
AA seq 736 aa
MAGSGAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMVPPAHEPRTDPAPPPPPVPPL
PPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVVSLRRERPRRRDSSERGAGGHRPS
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEEDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERASSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTARPEERAPESKSGSGSESEPSSRGGSLRRGGEPGGTGDGGPPPSRGSSGGAPNLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcggcgctgggggcggtggtgtcggggagacgaaggtgatttaccacctg
gatgaagaagagactccctacctggtgaagatccccgtccccgccgagcgcatcactctc
ggcgatttcaagagcgtcctgcagcggcccgcgggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagagatttcagatgacaatgctcgccttccctgc
ttcaacggaagggtggtatcctggttagtgtcatcagataacccccaacctgagatggtc
cccccagcccacgagcctcggacagacccggcgcctccaccgccacctgtaccccctctg
ccaccggagaggaccagtggcattggagactccaggcctccatccttccaccctaacgtg
tccagcagccgggaaaatctggagcccgagacagaaacagagtcagtggtgtctctgagg
cgggagcgacctcgcaggcgagacagcagtgagcgcggcgcggggggccaccggcccagc
ggcccctcgaggctggagcgccacctggcagggtacgagagctcctccaccctcatgacc
agcgagctggagagcaccagcctgggggactcggacgaggaggacaccatgagcaggttc
agcagctccacggagcagagcagcgcttctcgcctcctcaagcgccaccggcggcggagg
aaacagcggccaccccgcctggagagggcctcatccttcagcagcgtcaccgattccacc
atgtctctcaacatcatcacagtcacgctcaacatggagaagtacaacttcctgggcatc
tccatcgtgggtcagagcaacgagcggggagatggaggcatctacatcggctccatcatg
aagggtggggctgtggcggctgacgggcgcattgagcccggggacatgcttttgcaggtg
aacgacatgaactttgagaacatgagcaacgatgatgcggtgcgggtgctgagggatatc
gtgcacaagccgggccccatcgtgctgactgtagccaagtgctgggatccctcaccccag
gcctatttcactctcccccgaaatgagcccatccagccgattgaccctgctgcctgggtc
tcacactctgctgcgctgactggcaccttcccagcctatccaggctcctcgtccatgagc
accatcacatctgggtcctctcttcctgatggctgtgagggccggggcctctccatccat
acagacatggcatctgtgaccaaggccatggcagctccagagtctggactggaagttcgg
gaccgcatgtggctcaagatcaccatccctaacgcctttctgggctcggacgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgaaagtatgccagc
gggctgctcaaggcaggccttatccggcacactgtgaacaagatcaccttctctgagcag
tgctattacgtctttggagacctcagtggcggctgtgagagttacctagtcaacctgtct
ctgaatgacaacgatggctccagtggcgcttcggaccaggacaccttggctcctttgccc
ggagccaccccctggcctctgctgcccaccttctcctaccagtacccagccccgcatcca
tacagtccccagcccccaccctaccacgagctctcgtcctacacctacggcggaggcagt
gccagcagccagcacagtgaggggagccggagcagtgggtcgacacgaagcgatgggggg
gcggggcgcacagcgaggcccgaggagcgggcccctgagtccaagtctggcagcggcagt
gagtctgagccttccagccggggcggcagccttcggcggggtggggaacctggtgggact
ggtgatgggggccctcccccatccaggggctcatcaggaggcgctcccaatctccgagcc
cacccagggctccatccctatggtccacctcctggcatggccctcccgtataaccccatg
atggtggtcatgatgccccctcccccgccccctgtccctccagcagtgcagcctccaggg
gcccctccagtcagagacctgggctccgtgcccccagagctgacggccagccgccaaagc
ttccacatggccatgggcaaccccagtgagttctttgtggatgttatgtag

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