KEGG   Carlito syrichta (Philippine tarsier): 103263236
Entry
103263236         CDS       T07836                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
csyr  Carlito syrichta (Philippine tarsier)
Pathway
csyr04150  mTOR signaling pathway
csyr04310  Wnt signaling pathway
csyr04330  Notch signaling pathway
csyr04390  Hippo signaling pathway
csyr04550  Signaling pathways regulating pluripotency of stem cells
csyr04916  Melanogenesis
csyr04934  Cushing syndrome
csyr05010  Alzheimer disease
csyr05022  Pathways of neurodegeneration - multiple diseases
csyr05165  Human papillomavirus infection
csyr05200  Pathways in cancer
csyr05217  Basal cell carcinoma
csyr05224  Breast cancer
csyr05225  Hepatocellular carcinoma
csyr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:csyr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103263236 (DVL2)
   04330 Notch signaling pathway
    103263236 (DVL2)
   04390 Hippo signaling pathway
    103263236 (DVL2)
   04150 mTOR signaling pathway
    103263236 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103263236 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103263236 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103263236 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103263236 (DVL2)
   05226 Gastric cancer
    103263236 (DVL2)
   05217 Basal cell carcinoma
    103263236 (DVL2)
   05224 Breast cancer
    103263236 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103263236 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103263236 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    103263236 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103263236 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 103263236
NCBI-ProteinID: XP_008059113
Ensembl: ENSTSYG00000002261
UniProt: A0A1U7TRR2
LinkDB
Position
Unknown
AA seq 736 aa
MAGISSGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPELAPPAHEPRTELAPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLAPETETESVVSLRRERPRRRDSSEHGAGGHRPG
VPSRVERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRSLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLQRGGEPGGTGDGGPPPSRGSTGGAPNLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcatcagctcggggggcggtggggtcggggagacgaaggtgatttaccacctg
gatgaggaagagactccctacctggtgaagatccccgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgttctgcagcggcccgcgggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagaaatttcagatgacaatgcccgcctcccctgc
ttcaacggaagggtggtatcctggctagtgtcatcagataatccccaaccggagttggct
cctccagcccatgagcctcggacagaactggcacctccacccccacctttgccccctttg
ccacccgagaggaccagtggcattggggactcaaggcctccgtccttccaccctaatgtg
tccagtagccatgagaatctggcgcctgagacggaaaccgagtcagtagtgtcactgagg
cgggagaggcctcgcaggagagacagcagtgagcatggcgctgggggccacaggcctggt
gtcccttcaagggtggagcgccacctggcggggtacgaaagctcttctacgctcatgacc
agcgagctagagagtactagcctgggagactctgacgaggatgacaccatgagcaggttt
agcagctccacagagcagagcagtgcttcccgcctcctcaagcgccaccggcgacggagg
aaacagcggccaccccgcctggagaggacctcatccttcagcagtgtcacagattccaca
atgtctctcaacatcatcacagtcacactcaacatggagaagtacaacttcctgggcatc
tccattgtgggccaaagcaatgagcggggagatggaggcatctacatcgggtccatcatg
aagggtggggctgtggcggcagatggacgcattgagccaggggacatgcttttgcaggtg
aatgacatgaactttgagaacatgagcaatgatgatgccgtgcgggtactgagagacatt
gtgcacaagcctggccccatcgtgctgactgtggccaagtgctgggatccctctccccag
gcctatttcaccctcccccgaaatgagcccatccagccaattgaccctgctgcctgggtg
tcacactccgctgcactgactggcaccttcccagcctatccaggctcctcgtccatgagc
actattacatctggatcttctttgcctgatggctgcgagggccggagtctttccatccat
acggatatggcatctgtgaccaaggccatggcagctccagaatctgggctggaagtccgg
gaccgtatgtggctcaagatcaccatccctaatgcctttctgggctcagacgtagttgac
tggctctaccatcacgtggagggctttcctgaacggcgggaggcccgcaagtatgccagt
gggctgctgaaagcaggcctgatccgacacaccgtaaacaagatcaccttctctgagcag
tgctattatgtcttcggagacctcagtggtggctgtgagagttacctagtcaacctatct
ctgaatgacaacgatggctccagtggggcttcggaccaggacaccctggctcctctgcct
ggagccaccccctggcctctgctgcccaccttctcctaccagtacccagccccacacccc
tacagcccccagccaccaccctaccatgaactttcatcctatacctatggtgggggcagt
gccagcagccagcacagtgagggcagccggagcagtggttccacacgaagtgatgggggg
gcggggcgcacagggaggcctgaggagcgggcccctgagtctaaatccggcagtggcagt
gagtctgagccctccagtcgagggggcagccttcagcgtggcggggaacctggtgggact
ggtgatgggggccctcccccatccaggggctccactggaggtgctcccaacctccgagcc
catccagggctccatccctatggaccaccccctggcatggccctcccctataacccgatg
atggtggtcatgatgcctccccccccacctcctgtccctccagcagtgcagcccccaggg
gctcctccagtcagagacctgggctctgtgcccccagaactaacagccagccgccaaagc
ttccacatggccatgggcaatcccagtgagttctttgtggatgttatgtag

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