KEGG   Loxodonta africana (African savanna elephant): 100657749
Entry
100657749         CDS       T04351                                 
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
  KO
K02353  segment polarity protein dishevelled
Organism
lav  Loxodonta africana (African savanna elephant)
Pathway
lav04150  mTOR signaling pathway
lav04310  Wnt signaling pathway
lav04330  Notch signaling pathway
lav04390  Hippo signaling pathway
lav04550  Signaling pathways regulating pluripotency of stem cells
lav04916  Melanogenesis
lav04934  Cushing syndrome
lav05010  Alzheimer disease
lav05022  Pathways of neurodegeneration - multiple diseases
lav05165  Human papillomavirus infection
lav05200  Pathways in cancer
lav05217  Basal cell carcinoma
lav05224  Breast cancer
lav05225  Hepatocellular carcinoma
lav05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:lav00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100657749 (DVL2)
   04330 Notch signaling pathway
    100657749 (DVL2)
   04390 Hippo signaling pathway
    100657749 (DVL2)
   04150 mTOR signaling pathway
    100657749 (DVL2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100657749 (DVL2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100657749 (DVL2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100657749 (DVL2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100657749 (DVL2)
   05226 Gastric cancer
    100657749 (DVL2)
   05217 Basal cell carcinoma
    100657749 (DVL2)
   05224 Breast cancer
    100657749 (DVL2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100657749 (DVL2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100657749 (DVL2)
   05022 Pathways of neurodegeneration - multiple diseases
    100657749 (DVL2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100657749 (DVL2)
SSDB
Motif
Pfam: Dsh_C Dishevelled DIX DEP PDZ PDZ_6 Shufflon_N
Other DBs
NCBI-GeneID: 100657749
NCBI-ProteinID: XP_003416931
LinkDB
Position
Unknown
AA seq 736 aa
MAGSGAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMAPPAHEPRTDLVPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVVSLRRERPRRRDSSEHGGGGHRPS
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEPGPAGDGGPPPSRGSSGGPPNLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPIRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggcgggcagcggcgcggggggcggtggtgtcggggagacgaaggtgatttaccacttg
gatgaggaagagactccctatctagtgaagatccccgtccccgctgagcgcatcaccctc
ggcgatttcaagagcgtcctgcagcggcccgcgggagccaagtactttttcaagtctatg
gatcaggatttcggagtggtgaaggaagaaatttccgacgacaatgctcgccttccttgc
ttcaacggaagggtggtgtcctggctagtgtcatcagataacccccaacccgagatggct
cccccagcccatgagcctcgcacagacctggtgcctccacctccaccactaccccctttg
ccaccggagaggaccagtggcattggggactccaggcctccatctttccaccctaacgtc
tccagcagccgtgaaaacctggagccagagacagaaacagagtcagtcgtgtctctgagg
cgggagcggcctcgtaggagagacagcagtgagcacggcggtgggggccacaggcccagt
ggcccctcgaggctggagcgccacctagcagggtatgagagttcttccaccctgatgacc
agtgagctggagagcaccagcctgggggactcagatgaggatgacaccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctcctcaagcgccaccggcggcggagg
aaacagcgaccgccccgcctggagaggacctcatctttcagcagtgtcactgactccaca
atgtctcttaacatcatcacagtcacactcaacatggagaagtacaacttcctgggcatc
tccattgtgggccagagcaatgagcggggagacggtggcatctacatcggctccattatg
aagggtggggcggtggcagctgatgggcgcattgagcctggagacatgcttttacaggtg
aatgacatgaattttgagaacatgagcaacgatgatgcagtgcgggtgctgagggacatc
gtacacaagccaggccccattgtgctgactgtggccaagtgttgggatccctctccgcaa
gcctacttcacactcccccgaaatgagcctatccagccgattgatcctgctgcctgggtc
tcccactctgctgcgctgactggcaccttcccagcctatccaggctcctcatctatgagc
accattacatctggttcgtctctgcctgacggctgtgagggccggggtctctccatccat
acagacatggcgtctgtgaccaaggccatggcagctccagagtctggcctggaagttcga
gaccgcatgtggctcaagatcaccatcccgaatgcctttctgggctctgacgtggttgac
tggctctaccatcacgtggagggctttcccgaacggcgggaggcccgcaagtatgctagt
gggctgctcaaggcaggcctcattcggcacaccgtcaacaagatcaccttctctgaacag
tgctactatgtctttggagacctcagtggcggctgtgagagctatctagtcaacctgtct
ttgaatgacaacgatggctccagcggggcttcggaccaggacaccttggctcctctgcct
ggggccaccccctggcccttgttgcctactttctcctaccagtacccagcaccccaccca
tacagcccccagcccccaccctaccatgagctgtcctcctacacctatggtgggggcagt
gccagcagccagcacagtgagggaagccggagcagtgggtcaacacgaagcgatggtggg
gcagggcgcacggggaggcctgaggagcgggcccccgagtccaaatctggcagcggcagt
gagtctgagccctccagccgggggggcagtcttcgacggggcggggaacctggcccagct
ggtgatgggggtcctcccccatccaggggctcgtcagggggtccccccaatcttcgagcc
cacccagggctccatccctatggaccacccccaggcatggccctcccctataaccccatg
atggtggtcatgatgcccccacccccaccccctgtccccccagcagtgcagcccccgggg
gcccctcccatcagagacctgggctctgtgccccctgagctgacagccagccgccaaagc
ttccatatggccatgggcaaccccagtgagttctttgtggatgtgatgtag

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