KEGG   Sarcophilus harrisii (Tasmanian devil): 100931932
Entry
100931932         CDS       T02286                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2
  KO
K02353  segment polarity protein dishevelled
Organism
shr  Sarcophilus harrisii (Tasmanian devil)
Pathway
shr04150  mTOR signaling pathway
shr04310  Wnt signaling pathway
shr04330  Notch signaling pathway
shr04390  Hippo signaling pathway
shr04550  Signaling pathways regulating pluripotency of stem cells
shr04916  Melanogenesis
shr04934  Cushing syndrome
shr05010  Alzheimer disease
shr05022  Pathways of neurodegeneration - multiple diseases
shr05165  Human papillomavirus infection
shr05200  Pathways in cancer
shr05217  Basal cell carcinoma
shr05224  Breast cancer
shr05225  Hepatocellular carcinoma
shr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:shr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100931932 (DVL2)
   04330 Notch signaling pathway
    100931932 (DVL2)
   04390 Hippo signaling pathway
    100931932 (DVL2)
   04150 mTOR signaling pathway
    100931932 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100931932 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100931932 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100931932 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100931932 (DVL2)
   05226 Gastric cancer
    100931932 (DVL2)
   05217 Basal cell carcinoma
    100931932 (DVL2)
   05224 Breast cancer
    100931932 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100931932 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100931932 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    100931932 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100931932 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100931932
NCBI-ProteinID: XP_003768836
Ensembl: ENSSHAG00000008295
UniProt: G3W2D2
LinkDB
Position
4:complement(289206458..289213504)
AA seq 731 aa
MAGSGAAGLSGAGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYYFKS
MDQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDSSQPENNPPASEPRPEPASPPPPLPP
LPPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVISLRRERSRRRESIDHVGGSHRP
SGSARLERHLAGYESSSTLLTSELENTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRR
RKQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSI
MKGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLREIVHKPGPIVLTVAKCWDPSP
QAYFTLPRNEPIQPIDPAAWVSHSAALTGAFPTYPGSSSMSTITSGSSLPDGCEGRSLSI
HTDMASVTKAMAAPDSGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYA
SGLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPL
PGATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYSYGGGSAGSQHSEGSRSSGSTRSDG
GIGRTGRPEDRGPESKSGSGSESEPSSRAGSLHWGGDSSDATLPPPRGLGGGSSSLRSHP
TLHPYGPPSGVTLPYNPMMVVMMPPPPPPAVQPPGAPPVRDLGSVPPELTASRQSFHLAM
GNPSEFFVDVM
NT seq 2196 nt   +upstreamnt  +downstreamnt
atggcgggcagcggcgccgctggacttagcggggccggtgagacgaaggtgatttaccat
ctggacgaagaggaaactccgtacctggtcaagatcccggtcccggccgagcgcatcacc
ttgggagactttaagagcgtcctgcagcgccccgccggggccaaatactacttcaagtca
atggaccaggatttcggagtggtgaaggaagagatttcagatgacaatgccagattgccc
tgtttcaatgggagagtggtctcttggcttgtgtcctcagatagctcacagccagagaat
aaccccccagcctctgaacctcggccagaacccgcatctccacccccgccattgcctcct
ctgcctcctgagaggactagtggcataggggattcaaggcctccatcattccaccctaat
gtatctagtagccgagagaacctggagcctgagacagaaacagagtcagtgatatcactg
agacgggagcgatccaggaggagagagagcatcgatcacgttggtgggagccatcgacct
agtggttctgcccgcctggagcggcacctggctggttatgagagctcctctactcttcta
actagtgaattagagaataccagcctgggagattcagatgaggatgatactatgagcagg
ttcagtagctccacagagcagagcagtgcttcccgactcctaaagagacaccggcggagg
agaaaacagcgaccacctcgactggagaggacctcatccttcagcagtgtaacggattcc
accatgtctctcaacatcatcacagttactctcaacatggagaagtacaatttcctgggc
atctccattgtgggccaaagcaatgaacgtggcgatggcggcatctacattggctctatc
atgaagggtggtgctgtggctgcagatgggcgaattgaaccaggggacatgctactgcag
gtaaatgacatgaactttgagaacatgagtaatgatgatgctgtacgggtgctgagagag
attgtgcacaagcctggccccattgtgttaacagtagccaagtgttgggatccctcgcct
caggcttacttcacactccctagaaatgagccaatccagcctattgatcctgctgcctgg
gtctctcattcagcagcactcactggtgccttccctacctacccaggctcttcttccatg
agcaccataacttcaggttcctccctgcctgatggctgtgaaggacgaagcctctctata
cacacagacatggcgtctgtgaccaaggccatggcagcccccgactctgggttggaggtc
cgggaccgaatgtggctcaagataactatccctaatgcttttctgggctcagatgtagtg
gactggctttaccaccacgtagaggggttccctgagcggcgggaagcaaggaaatatgcc
agtgggttgctcaaggcaggcctcatccggcatactgtcaacaagatcaccttttctgaa
cagtgttactatgtcttcggggacctcagtgggggatgtgaaagctaccttgtgaatttg
tctctgaatgataatgatggatcaagtggagcttccgaccaggacacattggctcccctg
cctggggccacaccttggcccctgctgcctactttctcctaccagtacccagccccacat
ccctacagcccccagcctcccccttaccatgagctctcatcctacagctatggagggggc
agtgccggaagccagcatagtgaaggaagccggagcagtgggtctacgagaagtgatggg
ggaataggacggacagggagaccagaagatcggggtccagagtccaaatcaggcagtggg
agtgaatccgaaccatcaagccgtgctggcagcctccactggggtggggattccagtgat
gccactcttcctccacccaggggactaggtgggggtagcagcagccttcgttcccaccct
actctccatccctatgggccaccctctggagtgaccctaccatacaatcccatgatggta
gttatgatgcctcccccaccacctccagcagttcaacctcctggggcacctcctgtgcgt
gacttgggctctgtaccgcctgagctaactgccagccgccagagcttccatttagccatg
ggcaaccctagtgagttttttgtggatgtcatgtag

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