KEGG   Prionailurus bengalensis (leopard cat): 122484851
Entry
122484851         CDS       T07574                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
pbg  Prionailurus bengalensis (leopard cat)
Pathway
pbg04150  mTOR signaling pathway
pbg04310  Wnt signaling pathway
pbg04330  Notch signaling pathway
pbg04390  Hippo signaling pathway
pbg04550  Signaling pathways regulating pluripotency of stem cells
pbg04916  Melanogenesis
pbg04934  Cushing syndrome
pbg05010  Alzheimer disease
pbg05022  Pathways of neurodegeneration - multiple diseases
pbg05165  Human papillomavirus infection
pbg05200  Pathways in cancer
pbg05217  Basal cell carcinoma
pbg05224  Breast cancer
pbg05225  Hepatocellular carcinoma
pbg05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pbg00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    122484851 (DVL2)
   04330 Notch signaling pathway
    122484851 (DVL2)
   04390 Hippo signaling pathway
    122484851 (DVL2)
   04150 mTOR signaling pathway
    122484851 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    122484851 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    122484851 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122484851 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    122484851 (DVL2)
   05226 Gastric cancer
    122484851 (DVL2)
   05217 Basal cell carcinoma
    122484851 (DVL2)
   05224 Breast cancer
    122484851 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    122484851 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122484851 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    122484851 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    122484851 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX PDZ DEP PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 122484851
NCBI-ProteinID: XP_043438817
LinkDB
Position
E1:complement(2092925..2100689)
AA seq 742 aa
MAGSGAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDSARLPCFNGRVVSWLVSSDNPQPEVAPPAHEPRTELAPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVVSLRRDRPRRRDSSEHGAGGHRPG
GPSRLERHLAGYESSSTLMTSELESTSLGDSDDDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERASSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDVNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTMTSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSSGLRAGSDVVDWLYHHVEGFPERR
EARKYASGLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDDGSSGASDQD
TLAPLPGATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGS
TRSDGGAGRAGRPEERAPESKSGSGSESEPSTRGGSLRRGGDPGGAGDGGPPPSRGSSGG
APNLRAHPGLHPYGPPPGMALPYNPMMVVMVPPPPPPVPPAVQPPGAPPVRDLGSVPPEL
TASRQSFHMAMGNPSEFFVDVM
NT seq 2229 nt   +upstreamnt  +downstreamnt
atggcgggcagcggcgcggggggcggtggtgtcggggagacgaaggtgatttaccacctg
gatgaagaagagaccccgtacctggtgaagattcccgtccccgcggagcgcatcaccctg
ggcgatttcaagagcgtcctgcagcggcccgcgggcgctaagtactttttcaagtcaatg
gatcaggatttcggggtggtgaaggaggagatttcagatgacagcgcccgcctcccctgc
ttcaacggaagggtggtgtcctggctggtgtcgtcggacaacccccaacccgaggtggct
cccccagcccacgagcctcggaccgagctggcgccgccgccgccaccgttaccccctttg
ccgccggagaggaccagtggcattggcgactccagacctccgtccttccaccctaacgtg
tccagcagccgggaaaacctggagcccgagacagaaacggagtcggtggtgtctctgcgg
cgggaccggcctcgcaggagagacagcagtgagcatggcgcggggggccacaggcctggc
ggcccctcgaggctggagcgccacctggccgggtacgagagctcctcgacgctcatgacc
agcgagctggagagcaccagcctgggcgactctgacgacgacgacaccatgagcaggttc
agcagctccacggagcagagcagcgcctcccgcctcctgaagcgccaccggcggcggagg
aagcagcggccgccccgcctggagagggcctcgtccttcagcagtgtcaccgactccacc
atgtccctcaacatcatcacggtcacgctcaacatggagaagtacaacttcctgggcatc
tccatcgtgggccagagcaacgagcggggcgacggcggcatctacatcggctccatcatg
aaggggggcgccgtggcggccgacgggcgcatcgagccgggcgacatgttgctgcaggtg
aacgacgtgaacttcgagaacatgagcaatgacgacgcggtgcgggtgctgcgggacatc
gtgcacaagccgggccccatcgtgctgacggtggccaagtgctgggatccctctccccag
gcctacttcacccttcctcggaacgagcccatccagcccattgaccccgctgcctgggtg
tcccactccgccgcgctgacgggcaccttcccagcctatccgggctcctcgtccatgagc
accatgacatcggggtcctctctgcctgacggttgtgaggggcggggcctctccatccac
acagacatggcgtctgtgaccaaggccatggcagctcccgaatctggactggaagttcgg
gaccgcatgtggctcaagatcaccatccctaacgccttcctgggtagctccggtctccgg
gcaggctcggacgtagttgactggctttaccatcacgtggaaggctttcctgagcgccgg
gaggcccgcaaatacgccagcgggctgctcaaggctggcctcatccgacacacagtgaac
aaaatcaccttctctgagcagtgctattacgtgttcggggacctcagtggcggctgtgag
agctacctggtcaacctgtccctgaacgatgacggttccagcggggcttcggaccaggac
accttggcccctctgcctggggcgaccccgtggcccctgctgcccaccttctcctaccag
tacccggccccgcacccatacagcccccagccgccaccctaccatgagctctcatcctac
acctacggtgggggcagtgccagcagccagcacagcgaggggagccggagcagtgggtca
acacggagcgacgggggggcagggcgtgcggggaggcctgaggagcgggcccccgagtct
aagtccggcagcggcagtgagtccgagccctccacccgggggggcagccttcggcggggc
ggggaccctggtggagctggtgacgggggcccgcccccttccagaggctcttcggggggc
gcgcccaatctccgagcccaccctgggctgcatccctacggaccaccccctggcatggcc
ctcccctacaatcccatgatggtggtcatggtgcccccgccccctccccccgtgcctcca
gcagtgcagcccccgggggcccctccggtcagagacctgggctctgtgcccccggagctg
accgccagccgccagagcttccacatggccatgggcaaccccagtgagttctttgtggat
gttatgtag

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