KEGG   Microcebus murinus (gray mouse lemur): 105877972
Entry
105877972         CDS       T07238                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
mmur  Microcebus murinus (gray mouse lemur)
Pathway
mmur04150  mTOR signaling pathway
mmur04310  Wnt signaling pathway
mmur04330  Notch signaling pathway
mmur04390  Hippo signaling pathway
mmur04550  Signaling pathways regulating pluripotency of stem cells
mmur04916  Melanogenesis
mmur04934  Cushing syndrome
mmur05010  Alzheimer disease
mmur05022  Pathways of neurodegeneration - multiple diseases
mmur05165  Human papillomavirus infection
mmur05200  Pathways in cancer
mmur05217  Basal cell carcinoma
mmur05224  Breast cancer
mmur05225  Hepatocellular carcinoma
mmur05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mmur00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105877972 (DVL2)
   04330 Notch signaling pathway
    105877972 (DVL2)
   04390 Hippo signaling pathway
    105877972 (DVL2)
   04150 mTOR signaling pathway
    105877972 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105877972 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105877972 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105877972 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105877972 (DVL2)
   05226 Gastric cancer
    105877972 (DVL2)
   05217 Basal cell carcinoma
    105877972 (DVL2)
   05224 Breast cancer
    105877972 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105877972 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105877972 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    105877972 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105877972 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 105877972
NCBI-ProteinID: XP_012632495
Ensembl: ENSMICG00000004315
UniProt: A0A8B7H7I0
LinkDB
Position
16:55830770..55839790
AA seq 736 aa
MAGSSTGGCGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPPPEIAPPAHEPRTELVPPPPPLPPL
PPERTSGIGDSRPPSFHPNMSSSHENLEPETETESVVSLRRERPRRRDSSEHGAGGHRPA
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRMERSSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSESTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSIRWGGEPGGTGDGGPLPSRGSSGGAPNLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcagcacagggggctgtggggtcggggagacgaaggtgatttaccacctg
gatgaagaagagacgccctacctggtgaagatccccgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgttctgcagcggcccgcgggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaagaggaaatttcagacgacaatgcacgcctcccctgc
ttcaatggaagggtggtatcctggctagtgtcatcagataatcccccacctgagattgct
cctccagcccatgagcctcgaacagaactggtgcctcctcccccaccgttaccccctctg
ccaccggagaggactagcggcattggggactcgaggcctccatccttccaccctaatatg
tccagcagccatgaaaatctggagcctgagacggaaaccgagtcagtagtttcactgagg
cgagagcggccgcgcaggagagacagcagtgagcatggcgctgggggccacaggcctgct
ggcccctcaagactggagcgccacctggctgggtacgagagttcctctactcttatgacc
agtgagctggagagtacgagcctgggggactcggacgaggacgataccatgagcaggttc
agcagttccacagagcagagcagtgcctcccgcctccttaagcgccaccggcgacggagg
aaacagcggccaccccgcatggagaggagctcatccttcagcagcgtcacggattccacc
atgtctctcaacatcatcacagtcacgctcaacatggagaagtataacttcctgggcatc
tccattgtgggccaaagcaatgagcggggagacggaggcatctacatcggctccatcatg
aagggtggggctgtggcagccgatgggcgcatagagccaggggacatgcttttgcaggtg
aatgacatgaattttgagaacatgagcaatgatgatgctgtacgggtgctgagggacatt
gtgcacaagccgggccccatcgtgctgactgtggccaagtgctgggatccctccccccag
gcctatttcaccctcccccgaaatgagcccatccagccaattgaccctgctgcctgggtg
tcacactccgctgcactgactggtaccttcccagcctatccaggctcctcgtccatgagc
accatcacttctggatcttctttgcctgatggctgtgagggccggggcctctccatccat
acagatatggcatctgtgaccaaggcgatggcagctccagagtcggggctggaagtccgg
gaccgcatgtggctcaagatcaccatccctaatgcctttctgggctctgatgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggctcgcaagtatgccagc
gggctgctcaaggcaggcctgatccgacataccgtaaacaagatcaccttctctgagcag
tgctattatgtcttcggggacctcagcggtggctgtgagagttacctagtcaacctgtct
ctgaatgacaacgatggctccagtggggcttcagaccaggacaccctggctcctctgcct
ggggccaccccctggccccttctgcccaccttctcctaccaatacccagccccgcacccc
tacagcccccagcccccaccctaccatgagctttcatcgtacacctatggtgggggcagt
gccagcagccagcacagtgagggcagccggagcagtgagtcgacacgaagtgatgggggg
gcaggacgcacagggaggcccgaggagcgggcccctgagtccaagtccggcagtggcagt
gagtccgagccctccagcagagggggcagcatccgatggggtggggaacctggtgggact
ggtgatgggggtcctctcccctccagaggctcaagtgggggtgctcccaatctccgagcc
cacccagggctccatccctatggaccaccccctggcatggccctcccctataaccccatg
atggtggtcatgatgccgccacccccaccccctgtacccccagcagtgcagcccccgggg
gcccctccagtcagagacctgggctctgtgcccccagaactgacagccagccgccaaagc
ttccacatggccatgggcaaccccagtgagttctttgtggatgttatgtag

DBGET integrated database retrieval system