KEGG   Neogale vison (American mink): 122899331
Entry
122899331         CDS       T08764                                 
Symbol
DVL1
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-1 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04150  mTOR signaling pathway
nvs04310  Wnt signaling pathway
nvs04330  Notch signaling pathway
nvs04390  Hippo signaling pathway
nvs04519  Cadherin signaling
nvs04550  Signaling pathways regulating pluripotency of stem cells
nvs04916  Melanogenesis
nvs04934  Cushing syndrome
nvs05010  Alzheimer disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05165  Human papillomavirus infection
nvs05200  Pathways in cancer
nvs05217  Basal cell carcinoma
nvs05224  Breast cancer
nvs05225  Hepatocellular carcinoma
nvs05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    122899331 (DVL1)
   04330 Notch signaling pathway
    122899331 (DVL1)
   04390 Hippo signaling pathway
    122899331 (DVL1)
   04150 mTOR signaling pathway
    122899331 (DVL1)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    122899331 (DVL1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    122899331 (DVL1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    122899331 (DVL1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122899331 (DVL1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    122899331 (DVL1)
   05226 Gastric cancer
    122899331 (DVL1)
   05217 Basal cell carcinoma
    122899331 (DVL1)
   05224 Breast cancer
    122899331 (DVL1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    122899331 (DVL1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122899331 (DVL1)
   05022 Pathways of neurodegeneration - multiple diseases
    122899331 (DVL1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    122899331 (DVL1)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX PDZ DEP PDZ_6 Shufflon_N HTH_Rpn_C
Other DBs
NCBI-GeneID: 122899331
NCBI-ProteinID: XP_044092834
LinkDB
Position
2:complement(479112..490596)
AA seq 700 aa
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGVVK
EEISDDNAKLPCFNGRVVSWLVLAEGAHSDAGSQSTDGHTDRPPPLERTGGIGDSRPPSF
HPNVASSRDGMDNDTGTESLVSHRRERARRRNREEVARTNGHPRGDRRRDLGLPPDSASA
VLSSELESSSFIDSDEDDNTSRLSSSTEQSTSSRLIRKHKRRRRKQRLRQADRASSFSSI
TDSTMSLNIITVTLNMERHHFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDINFENMSNDDAVRVLREIVSQTGPISLTVAKCWDPTPRSYFTIPRADPVRPIDP
AAWLSHTAALTGALPRYGTSPCSSAVTRTSSSSLTSSVPGAPQLEETPLTVKSDMGAVVR
VMQLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFKERREARKYASSMLKRGFL
RHTVNKITFSEQCYYVFGDVCSNLAALNLNSGSSGASDQDTLAPLPHSAAPWPLGQGYPY
QYPGPPPCFPPAYQDPGFSYGSGSAGSQQSEGSKSSGSTRSAGGSSRRALGREKERRAAG
AGGSGSESDHTAPSGVGGGSWRERPASQLSRGSSPHSQASAAAPGLPPLYPLTKAYSVVG
GPPGGPPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq 2103 nt   +upstreamnt  +downstreamnt
atggcggagaccaagatcatctatcacatggacgaggaggagacgccgtacctggtcaag
ctgcccgtggcgcccgagcgcgtcacgctggccgacttcaagaacgtgctcagcaaccgg
cccgtgcacgcttacaaattcttcttcaagtccatggaccaggacttcggggtcgtgaag
gaggagatctccgatgataacgccaagctgccctgcttcaatggccgtgtggtctcctgg
ctggtcctggccgagggcgcacactcagatgccgggtctcagagcactgatggccacaca
gaccggcccccacctcttgagagaacgggcggcatcggggactcccggccaccctctttc
caccccaacgtagccagcagccgtgatgggatggacaatgacactggcacggagtctctg
gtcagccaccggcgggagcgagcccgacggcggaaccgtgaagaagttgcccggaccaat
gggcacccaaggggggaccggcggcgagacctggggctgccccccgacagtgcctctgcg
gtgctgagcagcgaactcgagtccagcagcttcatcgactccgatgaggatgacaacaca
agccgcctgagcagctccacggagcagagcacgtcctcccggctcatccggaagcacaag
cggaggcggcggaagcagcgcctgcggcaggcggaccgggcttcctccttcagcagcatc
acagactccaccatgtccctgaacatcatcaccgtcactctcaacatggagaggcaccac
ttcctgggtatcagcattgtgggccagagcaacgagcggggcgacggcggcatctacatc
ggctccatcatgaagggcggggccgtggcggccgacgggcgcatcgagccgggggacatg
ctgctgcaggtaaacgacatcaacttcgagaacatgagcaacgatgacgcggtgcgggtg
ctgcgggagatcgtgtcccagacggggcccatcagcctcacggtggccaagtgctgggac
ccgaccccccggagctacttcaccatcccgagggctgacccggtccggcccatcgacccc
gccgcctggctgtcccacacggcggcgctgaccggagccctgccgcgctatggtacgagc
ccctgctccagtgctgtcacacgcaccagctcctcctcactaaccagctctgtgccgggc
gctccacaactggaggagacgcctctgaccgtgaagagtgacatgggcgccgtggtgcgc
gtcatgcagctgccagactcgggcctggagatccgagaccgcatgtggctcaagatcacc
atcgccaacgctgtcatcggggcggacgtggtggactggctgtacacgcacgtggagggc
ttcaaggagcggcgcgaggctcgcaagtacgccagcagcatgctgaagcggggcttcctg
cggcacacggtcaacaagatcaccttctcggagcagtgctactacgtcttcggggacgtg
tgcagcaatctcgcagccctgaacctcaacagcggctccagcggggcctcggatcaggac
acgctggcccccctgccccattcggccgccccgtggcccctgggtcagggctacccctac
cagtacccgggccccccgccctgcttcccacctgcgtaccaggaccctggcttcagctat
ggtagcggcagcgcaggaagtcagcagagcgaaggaagcaaaagcagtgggtccacccgg
agcgccggcgggagcagccggcgggcactgggccgtgagaaggagcgccgggcggctgga
gccggaggcagtggcagcgagtcggaccacacggcgccgagtggggtcggtggtggcagc
tggcgggagcgtccggctagccagctcagccggggcagcagcccacacagccaggcctcg
gctgctgccccggggctacccccactgtatcccttaacaaaggcttactcagtggtgggg
gggccaccaggggggccgcctgtccgggagctggctgctgttcccccagagctgacaggc
agccgccagtccttccagaaggccatgggaaacccctgtgaattttttgttgacatcatg
tga

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