Rousettus aegyptiacus (Egyptian rousette): 107507013
Help
Entry
107507013 CDS
T06036
Gene name
DVL3
Definition
(RefSeq) segment polarity protein dishevelled homolog DVL-3 isoform X1
KO
K02353
segment polarity protein dishevelled
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150
mTOR signaling pathway
ray04310
Wnt signaling pathway
ray04330
Notch signaling pathway
ray04390
Hippo signaling pathway
ray04550
Signaling pathways regulating pluripotency of stem cells
ray04916
Melanogenesis
ray04934
Cushing syndrome
ray05010
Alzheimer disease
ray05022
Pathways of neurodegeneration - multiple diseases
ray05165
Human papillomavirus infection
ray05200
Pathways in cancer
ray05217
Basal cell carcinoma
ray05224
Breast cancer
ray05225
Hepatocellular carcinoma
ray05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
107507013 (DVL3)
04330 Notch signaling pathway
107507013 (DVL3)
04390 Hippo signaling pathway
107507013 (DVL3)
04150 mTOR signaling pathway
107507013 (DVL3)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
107507013 (DVL3)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
107507013 (DVL3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
107507013 (DVL3)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
107507013 (DVL3)
05226 Gastric cancer
107507013 (DVL3)
05217 Basal cell carcinoma
107507013 (DVL3)
05224 Breast cancer
107507013 (DVL3)
09164 Neurodegenerative disease
05010 Alzheimer disease
107507013 (DVL3)
05022 Pathways of neurodegeneration - multiple diseases
107507013 (DVL3)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
107507013 (DVL3)
09172 Infectious disease: viral
05165 Human papillomavirus infection
107507013 (DVL3)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
DEP
PDZ
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
107507013
NCBI-ProteinID:
XP_015993468
LinkDB
All DBs
Position
Unknown
AA seq
754 aa
AA seq
DB search
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPEPAPFCADNPSELPPPMERTGGIGDSRPPSFHPH
AGGGSQENLDNDTETDSLVSAQRERPRRRDGPEHTARLNGTAKGERRRDPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGYGWDGHYRRGGRHFWLSGKGFGLASTHPALTRD
TLAFRPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAAWVSHTAAMTGTFPAYGMSPSLS
TITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMASPESGLEVRDRMWLKITIPNAF
IGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHTVNKITFSEQCYYIFGDLCGNMA
NLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQYPPPPHPYNPHPGFPELGYSYGG
GSASSQHSEGSRSSGSNRSGSDRRKEKDPKAGDSKSGGSGSESDHTTRSSLRGPRERAPS
ERSGPTASEHSHRSHHSLASSLRSHHTHPSYGPPGVPPLYGPPMLMMPPPPAAMGPPGAP
PGRDLASVPPELTASRQSFRMAMGNPSEFFVDVM
NT seq
2265 nt
NT seq
+upstream
nt +downstream
nt
atgggagagaccaagatcatctaccacctggacgggcaggagacgccgtacctggtgaag
ctgcccctgcccgccgagcgcgtcaccttggcggactttaagggcgttctgcagcgaccc
agctataagttcttcttcaagtctatggacgacgatttcggagtggtgaaggaagagatc
tcagatgacaatgcaaagctgccctgcttcaatggccgggtggtgtcctggctggtgtca
gctgagggctcacacccagagccagctcccttttgtgctgataacccatcagagctgcca
ccacccatggagcgcacaggaggcattggggactcccggcccccatccttccaccctcat
gctggtgggggcagccaggagaacctggacaatgatacagagacggactcattggtgtct
gcccagcgggagcggccacgcaggagggacggcccagagcacacagcccggctaaatgga
actgcaaagggggaacgacggcgagatccagggggttatgacagctcatccaccctcatg
agcagtgaattggagaccaccagcttctttgattcagatgaagatgactctaccagcagg
ttcagcagctccacagagcagagcagcgcctcacgcctgatgagaagacacaagcggcgg
cggcggaagcagaaggtttcccggattgagcggtcctcgtccttcagcagcatcacggac
tccaccatgtcactcaacatcatcacggtcactctcaacatggaaaagtataacttcttg
ggcatctccattgtgggccaaagcaacgagcgtggtgacggaggcatctacattggctct
atcatgaagggtggggctgtggctgctgatggacgcatcgagccaggagatatgctgtta
caggtaaacgagatcaactttgagaacatgagtaatgatgacgcggtccgggtactgcgg
gagattgtgcacaaaccagggtatggatgggatgggcattacagaagaggaggcagacat
ttctggctctcaggcaaggggtttggtctggcctccacacatcctgccctcactagggac
acccttgctttcaggcccatcaccctgactgtagccaagtgctgggacccaagcccacgt
ggttgcttcacactgcccaggagcgagcccatcaggcccattgaccctgcggcctgggtc
tctcacactgcagccatgactggcaccttccctgcctacggcatgagcccctccctgagc
accatcacctccaccagctcctccatcaccagctccatccctgacacagagcggctagat
gatttccacctgtccatccacagtgacatggctgccattgtgaaagccatggcctcccct
gaatccgggttggaggtccgagaccgcatgtggctcaagatcaccatccccaatgctttc
atcggctcggatgtggtggactggctgtaccacaacgtggaaggcttcactgaccggcga
gaggcccgcaagtacgccagcaacctgctgaaagctggcttcattcgccacactgtgaac
aagatcactttctccgagcagtgctactacatcttcggcgacctttgcggcaacatggcc
aacctgtctctccatgatcatgatggctctagtggtgcctctgaccaggacacgctggcc
cctttgccgcaccccggggccgccccttggcccatggctttcccttaccagtacccacca
cccccgcacccttacaacccgcatccaggctttcctgagctggggtacagctacggcggg
ggcagcgctagcagtcagcacagtgaaggcagccggagcagtggctccaaccgtagtggc
agcgaccggcggaaagagaaggacccgaaggctggggactcaaagtccggaggcagtggc
agcgagtcggaccacacaacccgcagcagccttcgggggccgcgagagcgggcgcccagc
gagcgctcagggcctactgccagcgagcatagccaccgtagccaccactcgctggccagc
agcctgcgcagccaccacacgcacccaagctacggtccccctggtgtgccccctctctac
ggccctcctatgctgatgatgcccccaccgcctgcggccatgggacccccaggagcccct
cctggccgtgacctggcctcggtgccccctgaactgaccgccagcagacagtccttccgc
atggccatgggaaaccccagtgagttctttgtggatgtgatgtga
Rousettus aegyptiacus (Egyptian rousette): 107509513
Help
Entry
107509513 CDS
T06036
Gene name
DVL2
Definition
(RefSeq) segment polarity protein dishevelled homolog DVL-2 isoform X1
KO
K02353
segment polarity protein dishevelled
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150
mTOR signaling pathway
ray04310
Wnt signaling pathway
ray04330
Notch signaling pathway
ray04390
Hippo signaling pathway
ray04550
Signaling pathways regulating pluripotency of stem cells
ray04916
Melanogenesis
ray04934
Cushing syndrome
ray05010
Alzheimer disease
ray05022
Pathways of neurodegeneration - multiple diseases
ray05165
Human papillomavirus infection
ray05200
Pathways in cancer
ray05217
Basal cell carcinoma
ray05224
Breast cancer
ray05225
Hepatocellular carcinoma
ray05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
107509513 (DVL2)
04330 Notch signaling pathway
107509513 (DVL2)
04390 Hippo signaling pathway
107509513 (DVL2)
04150 mTOR signaling pathway
107509513 (DVL2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
107509513 (DVL2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
107509513 (DVL2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
107509513 (DVL2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
107509513 (DVL2)
05226 Gastric cancer
107509513 (DVL2)
05217 Basal cell carcinoma
107509513 (DVL2)
05224 Breast cancer
107509513 (DVL2)
09164 Neurodegenerative disease
05010 Alzheimer disease
107509513 (DVL2)
05022 Pathways of neurodegeneration - multiple diseases
107509513 (DVL2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
107509513 (DVL2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
107509513 (DVL2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
PDZ
DEP
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
107509513
NCBI-ProteinID:
XP_015997580
LinkDB
All DBs
Position
Unknown
AA seq
736 aa
AA seq
DB search
MAGSGAGVSGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNSQPEMTPSAQEPRTELAPPPPPLPPL
PPERTSGIGDSRPPSFHPNVSSSRENLEPETETESVVSLRRERPRRRDSSEHGAGGHRPN
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEDDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCENYLVNLSLNDNDGSSGASDQDTLAPLP
GTTPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSARSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGDPSGTGDGGPPLSRSSSGGTPSHQA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPAAPPVVQPPGAPPIRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq
2211 nt
NT seq
+upstream
nt +downstream
nt
atggcgggcagcggcgcgggggttagtggtgtcggagagacgaaggtgatttaccatttg
gatgaagaagagactccctacctggtgaagatccccgtccctgccgagcgcatcaccctt
ggcgattttaagagcgtactgcagcgacccgcgggcgctaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagaaatttcagatgacaatgcccgccttccctgc
ttcaacggaagggtggtttcctggctcgtgtcatcggataactcccagcctgagatgact
ccctcagctcaggaacctcggacagaactggcacctccacccccaccattaccccctttg
ccaccagagaggaccagtggcattggggattctagacctccatccttccaccctaatgtt
tcgagcagccgggaaaatctggagcctgagacagaaacagagtcagtagtgtctctgagg
cgggagcggcctcggagaagagacagcagtgagcatggcgctgggggccacaggcccaac
ggcccctctaggctggagcgccacctggctgggtacgagagctcctcaacccttatgact
agcgagctggagagcactagcctaggggactcagatgaggatgataccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctcctcaagcgtcaccggcggcgaagg
aaacagcggccaccccgtctggagaggacctcatccttcagcagtgtcactgattccaca
atgtctctcaacatcatcacagtcacactcaacatggagaagtacaacttcctgggcatc
tccattgtgggccaaagcaatgagcggggagacgggggcatctacatcggctccatcatg
aagggtggggctgtggcggctgatggacgcattgagcctggggacatgcttttgcaggtg
aatgacatgaactttgagaacatgagcaatgatgatgcggtgcgggtgctgagagacatt
gtgcacaagccaggccccattgtgctgactgtggccaagtgctgggatccctctcctcag
gcttatttcactcttcctcgaaatgagcccatccagccaattgaccccgctgcctgggtc
tcacattctgctgcactgactggcaccttcccagcttatccaggctcctcctccatgagc
accattacatctgggtcctctttacctgatggttgtgagggccggggtctctccatccat
acagacatggcatctgtgactaaagccatggcagctccagagtctggactagaagttcgg
gaccgtatgtggctcaagatcaccattcctaatgcctttctcggctcagatgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgcaagtatgccagt
ggactgctaaaggcaggccttatccgacacacagtaaacaagatcaccttctctgagcag
tgctattacgtcttcggagacctcagtggtggctgtgagaattatttagtcaacctgtct
ttgaatgataatgatggctccagtggggcttcggatcaggacaccttggctcctctgcct
gggaccaccccctggcccctgctgcccaccttctcctaccagtacccagccccacaccca
tacagcccccagcccccaccctaccatgaactctcatcctatacctatggtggaggcagt
gctagcagccagcacagtgaagggagccggagcagtgggtccgcacgaagcgatgggggg
gcagggcgcacagggaggcctgaggagcgggcccctgagtccaagtccggcagcggcagt
gagtccgagccctccagccgggggggcagccttcggcgaggcggggatcctagtggcact
ggtgatgggggccctcccctttccaggagctcatcagggggtactcccagtcaccaagcc
cacccagggctccatccctatggtccaccccctggtatggccctcccctataaccccatg
atggtggtcatgatgcccccacctcctccagctgcccctccagtagtgcaacccccaggg
gcccctcccatcagagacctgggctcagtgcccccagagctgacagccagccgccaaagc
ttccacatggccatgggcaaccccagtgagttctttgtggatgttatgtag
Rousettus aegyptiacus (Egyptian rousette): 107510646
Help
Entry
107510646 CDS
T06036
Gene name
DVL1
Definition
(RefSeq) LOW QUALITY PROTEIN: segment polarity protein dishevelled homolog DVL-1
KO
K02353
segment polarity protein dishevelled
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150
mTOR signaling pathway
ray04310
Wnt signaling pathway
ray04330
Notch signaling pathway
ray04390
Hippo signaling pathway
ray04550
Signaling pathways regulating pluripotency of stem cells
ray04916
Melanogenesis
ray04934
Cushing syndrome
ray05010
Alzheimer disease
ray05022
Pathways of neurodegeneration - multiple diseases
ray05165
Human papillomavirus infection
ray05200
Pathways in cancer
ray05217
Basal cell carcinoma
ray05224
Breast cancer
ray05225
Hepatocellular carcinoma
ray05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
107510646 (DVL1)
04330 Notch signaling pathway
107510646 (DVL1)
04390 Hippo signaling pathway
107510646 (DVL1)
04150 mTOR signaling pathway
107510646 (DVL1)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
107510646 (DVL1)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
107510646 (DVL1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
107510646 (DVL1)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
107510646 (DVL1)
05226 Gastric cancer
107510646 (DVL1)
05217 Basal cell carcinoma
107510646 (DVL1)
05224 Breast cancer
107510646 (DVL1)
09164 Neurodegenerative disease
05010 Alzheimer disease
107510646 (DVL1)
05022 Pathways of neurodegeneration - multiple diseases
107510646 (DVL1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
107510646 (DVL1)
09172 Infectious disease: viral
05165 Human papillomavirus infection
107510646 (DVL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Dishevelled
Dsh_C
PDZ
DIX
DEP
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
107510646
NCBI-ProteinID:
XP_015999848
LinkDB
All DBs
Position
Unknown
AA seq
757 aa
AA seq
DB search
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGSVG
RGPVRGRGCWHLSALGQGLGDPGAAPRRGVSTCLWVVDSGGQRRLQTCFNGPAWSPLGGP
ALAAWQWRALRRRGEAGHRAPRAPWVWPRGCRASPSHCSPPQLVLAEGAHSDAGSQATDG
HADLPPPLERMGGIGDSRPPSFHPNVASSREGMDNETGTESMVSHRRERARRRNREEAAR
TNGHPRGDRRRDLGLPPDSASTVLSSELESSSFIDXDEDGSTSRLSSSTEQSTSSRLIRK
HKRRRRKQRLRQTDRASSFSSSITDSTMSLNIITVTLNMERHHFLGISIVGQSNDRGDGG
IYIGSIMKGGAVAADGRIEPGDMLLQVNDVNFENMSNDDAVRVLREIVSQTGPISLTVAK
CWDPTPRSYFTIPRADPVRPIDPAAWLSHAAALAGARPLYELEEGPLTVKSDMGAVVRVM
QLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFKERREARRYASSMLKHGFLRH
TVNKVTFSEQCYYVFGDLCSSLAALTLHSGSSGASDQDMLAPLPHPAAPWPLGQGYPYQY
PGPPPCFPPAYQDPGFSYGSGSAGSQQSEGSKSSGSTRSAGGSSRRALGREKEHRGAGAG
GSGSESDHTAPSGVGGSGWRERPVSQLSRGSSPHSQASAAPGLPPLHPLTKAYSVVGGPP
GGPPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq
2274 nt
NT seq
+upstream
nt +downstream
nt
atggcggagaccaagatcatctatcacatggatgaggaggagacgccgtacctggtcaag
ctgcccgtggcgcctgagcgcgtcacgctggccgacttcaagaacgtgctcagcaaccgg
ccagtgcacgcctacaaattcttcttcaagtccatggaccaggacttcgggtcagtgggc
cgtgggcctgtgcgcgggcgcgggtgttggcacctgtcggcgcttgggcagggccttggg
gatcctggggccgcgccccggcgtggcgtgtccacctgtctgtgggtggtagattctgga
ggacagcgcaggctgcagacctgcttcaacggccctgcgtggtctcctttgggtggccct
gcactggcggcgtggcagtggcgggcactccggcggaggggggaggccggccaccgcgcc
ccgcgggccccgtgggtgtggcctaggggctgccgggcttccccgagccactgctctcct
ccgcagctggtcctggctgagggcgcccactcggatgcagggtctcaggccactgacgga
cacgcagacctgcccccgcctctggagcggatgggtggcatcggggactcccggcccccc
tctttccacccgaatgtggccagcagccgtgaagggatggacaatgagactggtaccgag
tccatggtcagccacaggcgggagcgagcccggcgccggaaccgtgaggaggctgcccgg
accaacgggcacccgaggggggaccggcggcgggacctggggctgccccccgacagtgcg
tccaccgtgctgagcagcgaactcgagtccagtagcttcatcgacncagacgaggatggc
agcacgagccggctgagcagctccacggagcagagcacctcctcccggctcatccggaag
cacaagcggcggcggcggaagcagcgcttgcggcagacggaccgcgcctcctccttcagc
agcagcatcacggactccaccatgtccctgaacatcatcaccgtcacgctcaacatggag
aggcaccacttcctgggcatcagcatcgtgggccagagcaacgaccggggtgacggcggc
atctacatcggctccatcatgaagggcggggccgtggctgcggacggccggatcgagccc
ggcgacatgctgctgcaggtgaacgacgtcaacttcgagaacatgagcaacgacgacgct
gtgcgggtgctgcgggagatcgtgtcgcagacggggcccatcagcctcacagtggccaag
tgctgggacccaacgccccggagctatttcaccatcccgagggctgacccggtgcggccc
atcgacccggccgcctggctgtcccacgcagcggcgctggccggagcccggcccctgtac
gagctggaggaggggccgctgacggtgaagagcgacatgggcgccgtggtccgggtcatg
cagctgccggactccggcctggagatccgcgaccggatgtggctcaagatcaccattgcc
aatgctgtcattggcgcggacgtggtggactggctgtacacgcacgtggaaggcttcaag
gagcgcagggaggcacgcaggtacgccagcagcatgctcaagcacggcttcctgaggcac
acggtcaacaaggtcaccttctccgagcagtgctactacgtcttcggggacctgtgcagc
agtctcgccgccctgaccctccacagcggctccagtggggcctcggaccaggacatgctg
gccccgctgccccacccggctgccccctggcccctgggccagggctacccctaccagtac
ccggggcccccgccctgcttcccgcccgcgtaccaggaccccggcttcagctacggcagc
ggcagtgctgggagtcagcagagtgaaggaagcaaaagcagcgggtccacccggagtgcg
ggcgggagcagccggcgggccctgggccgagagaaggagcatcgcggggctggagctgga
ggcagcggcagcgagtcagaccacacagccccgagtggagtcgggggcagcgggtggcgg
gagcgtccagtgagccagctcagtcgtggcagcagcccgcatagccaggcctcggcggcc
ccagggctccccccactgcatcccctgacgaaggcatactcagtggtgggcgggccgcct
ggggggcctcccgtccgggagctggccgctgtccccccagagctgacgggcagccgccag
tccttccagaaggccatggggaatccctgtgaattcttcgtcgacatcatgtga
DBGET
integrated database retrieval system