Nomascus leucogenys (northern white-cheeked gibbon): 100583216
Help
Entry
100583216 CDS
T03265
Symbol
DVL3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3
KO
K02353
segment polarity protein dishevelled
Organism
nle
Nomascus leucogenys (northern white-cheeked gibbon)
Pathway
nle04150
mTOR signaling pathway
nle04310
Wnt signaling pathway
nle04330
Notch signaling pathway
nle04390
Hippo signaling pathway
nle04550
Signaling pathways regulating pluripotency of stem cells
nle04916
Melanogenesis
nle04934
Cushing syndrome
nle05010
Alzheimer disease
nle05022
Pathways of neurodegeneration - multiple diseases
nle05165
Human papillomavirus infection
nle05200
Pathways in cancer
nle05217
Basal cell carcinoma
nle05224
Breast cancer
nle05225
Hepatocellular carcinoma
nle05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
nle00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100583216 (DVL3)
04330 Notch signaling pathway
100583216 (DVL3)
04390 Hippo signaling pathway
100583216 (DVL3)
04150 mTOR signaling pathway
100583216 (DVL3)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100583216 (DVL3)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100583216 (DVL3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100583216 (DVL3)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100583216 (DVL3)
05226 Gastric cancer
100583216 (DVL3)
05217 Basal cell carcinoma
100583216 (DVL3)
05224 Breast cancer
100583216 (DVL3)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100583216 (DVL3)
09164 Neurodegenerative disease
05010 Alzheimer disease
100583216 (DVL3)
05022 Pathways of neurodegeneration - multiple diseases
100583216 (DVL3)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100583216 (DVL3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
DEP
PDZ
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
100583216
NCBI-ProteinID:
XP_030678751
Ensembl:
ENSNLEG00000006124
LinkDB
All DBs
Position
11:105299489..105314772
Genome browser
AA seq
716 aa
AA seq
DB search
MGETKIIYHLDGQETPYLVKLPLPAERVTLADFKGVLQRPSYKFFFKSMDDDFGVVKEEI
SDDNAKLPCFNGRVVSWLVSAEGSHPDPAPFCADNPSELPPPMERTGGIGDSRPPSFHPH
AGGGSQENLDNDTETDSLVSAQRERPRRRDGPEHATRLNGTAKGERRREPGGYDSSSTLM
SSELETTSFFDSDEDDSTSRFSSSTEQSSASRLMRRHKRRRRKQKVSRIERSSSFSSITD
STMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIMKGGAVAADGRIEPGDMLL
QVNEINFENMSNDDAVRVLREIVHKPGPITLTVAKCWDPSPRGCFTLPRSEPIRPIDPAA
WVSHTAAMTGTFPAYGMSPSLSTITSTSSSITSSIPDTERLDDFHLSIHSDMAAIVKAMA
SPESGLEVRDRMWLKITIPNAFIGSDVVDWLYHNVEGFTDRREARKYASNLLKAGFIRHT
VNKITFSEQCYYIFGDLCGNMANLSLHDHDGSSGASDQDTLAPLPHPGAAPWPMAFPYQY
PPPPHPYNPHPGFPELGYSYGGGSASSQHSEGSRSSGSNRSGSDRRKEKDPKAGDSKSGG
SGSESDHTTRSSLRGPRERAPSERSGPAASEHSHRSHHSLASSLRSHHTHPSYGPPGVPP
LYGPPMLMMPPPPAAMGPPGAPPGRDLASVPPELTASRQSFRMAMGNPSEFFVDVM
NT seq
2151 nt
NT seq
+upstream
nt +downstream
nt
atgggcgagaccaagatcatctaccacttggatgggcaggagacgccgtaccttgtgaag
ctgcccctgcctgccgagcgcgtcaccttggcggactttaagggcgttttgcagcgaccc
agctataagttcttcttcaagtctatggacgacgatttcggagtggtgaaggaggagatc
tcggatgacaatgccaagctaccgtgcttcaatggccgggtggtgtcctggctggtgtca
gctgagggctcacacccagacccagcccccttctgtgctgacaacccatcggagctgcca
ccacctatggagcgcacgggaggcatcggggactcccgacccccatccttccaccctcat
gctggtgggggcagccaggagaacctggacaatgacacagagacggactctttggtgtct
gcccagcgagagcggccacgccggagggatggcccagagcatgcaacccggctaaatgga
actgcgaagggggagcggcggcgagaaccagggggttatgatagctcatccacccttatg
agcagcgagctggagaccaccagcttctttgactcagatgaggatgactccaccagcagg
ttcagcagctccacagaacagagcagcgcctcacgcctgatgagaagacacaagcggcgg
cggcggaagcagaaggtttctcggattgagcggtcctcgtccttcagcagcatcacggac
tccaccatgtcactcaacatcatcacggtcactctcaacatggagaaatataacttcttg
ggcatctccatcgtgggccaaagcaacgagcgtggtgacggcggcatctacattggctct
atcatgaagggtggagccgtggctgctgatggacgcatcgagccaggagatatgctgtta
caggtaaacgagatcaactttgagaacatgagtaatgacgatgcagtccgggtactgcgg
gagattgtgcacaaaccggggcccatcaccctgactgtagccaagtgctgggacccaagt
ccacgtggttgcttcacattgcccaggagcgagcccatccggcccattgaccctgcggcc
tgggtctcccacactgcagccatgaccggcaccttccctgcatacggcatgagcccctcc
ctgagcaccatcacctccaccagctcctccatcaccagttccatccctgacacagagcgc
ctagacgacttccacttgtccatccacagtgacatggctgccatcgtaaaagccatggcc
tcccctgaatcagggttggaggtccgtgaccgcatgtggctcaagattaccatccctaat
gctttcatcggctcagatgtggtggactggctgtaccacaatgtggaaggcttcacggac
cggagggaggcccgcaagtatgccagcaacctgctgaaagctggcttcatccgccatacc
gtcaacaagatcaccttctccgagcagtgctactacatcttcggcgacctctgcggcaac
atggccaacctgtctctccacgatcacgatggctccagtggcgcttctgaccaggacaca
ctggcccctttgccgcacccgggggccgccccttggcccatggctttcccgtaccagtac
ccgccacccccgcacccctacaacccccacccgggcttcccggagctgggctacagctac
ggcgggggcagcgccagcagtcagcacagcgaaggcagtcggagcagtggctccaaccgt
agcggcagcgatcggaggaaggagaaggacccgaaggccggggactccaagtctgggggc
agcggcagcgaatcggaccacaccacacgcagcagcctgcgggggccgcgggagcgggcg
cccagcgagcgctcagggccagcggccagcgagcacagccaccgcagccaccattccctg
gccagcagccttcgcagccaccacacccacccaagctacggccctcccggagtgccccct
ctctacggcccccccatgctgatgatgcccccgccgcccgcggccatggggcccccagga
gcccctccgggccgcgacctggcctcagtgcccccggaactgaccgccagcagacaatcc
ttccgcatggccatgggaaaccccagtgagttctttgtggatgtgatgtga
Nomascus leucogenys (northern white-cheeked gibbon): 100585595
Help
Entry
100585595 CDS
T03265
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2
KO
K02353
segment polarity protein dishevelled
Organism
nle
Nomascus leucogenys (northern white-cheeked gibbon)
Pathway
nle04150
mTOR signaling pathway
nle04310
Wnt signaling pathway
nle04330
Notch signaling pathway
nle04390
Hippo signaling pathway
nle04550
Signaling pathways regulating pluripotency of stem cells
nle04916
Melanogenesis
nle04934
Cushing syndrome
nle05010
Alzheimer disease
nle05022
Pathways of neurodegeneration - multiple diseases
nle05165
Human papillomavirus infection
nle05200
Pathways in cancer
nle05217
Basal cell carcinoma
nle05224
Breast cancer
nle05225
Hepatocellular carcinoma
nle05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
nle00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100585595 (DVL2)
04330 Notch signaling pathway
100585595 (DVL2)
04390 Hippo signaling pathway
100585595 (DVL2)
04150 mTOR signaling pathway
100585595 (DVL2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100585595 (DVL2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100585595 (DVL2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100585595 (DVL2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100585595 (DVL2)
05226 Gastric cancer
100585595 (DVL2)
05217 Basal cell carcinoma
100585595 (DVL2)
05224 Breast cancer
100585595 (DVL2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100585595 (DVL2)
09164 Neurodegenerative disease
05010 Alzheimer disease
100585595 (DVL2)
05022 Pathways of neurodegeneration - multiple diseases
100585595 (DVL2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100585595 (DVL2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
DEP
PDZ
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
100585595
NCBI-ProteinID:
XP_004092705
Ensembl:
ENSNLEG00000008027
LinkDB
All DBs
Position
19:70549174..70558790
Genome browser
AA seq
736 aa
AA seq
DB search
MAGSSTGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMAPPAHEPRAELAPPAPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERPRRRDSSEHGAGGHRTG
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEEDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEPSGTSDGGPPPSRGSTGGAANLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq
2211 nt
NT seq
+upstream
nt +downstream
nt
atggcgggcagcagcactgggggcggtggggttggggagacgaaggtgatttaccatctg
gatgaggaagagactccctacctggtgaagatccctgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgtcctgcagcggcccgcaggcgccaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagaaatttcagatgacaacgcccgcctcccctgc
ttcaacggaagggtggtatcctggctggtgtcctcagataatccccaacccgagatggcc
cctccagcccatgagcctcgggcagaactggcgcctccagccccacctttaccccctttg
ccacccgagaggaccagcggcattggggactcaaggcctccatccttccaccctaatgtg
tccagcagccatgagaatctggagcctgagacagaaaccgagtcagtagtgtcactgagg
cgggagcggcctcgcaggagagacagcagtgagcatggcgctgggggccacaggactggt
ggcccctcaaggctggagcgccacctggccggatacgagagctcctctaccctcatgacc
agcgagctggagagtaccagcctgggggactcagatgaggaggacaccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctccttaagcgccaccggcggcgaagg
aagcagcggccaccccgcctggagaggacgtcgtccttcagcagcgtcacagattccaca
atgtctctgaatatcatcacagtcacgctaaacatggagaagtacaacttcctgggtatc
tccatcgtgggccaaagcaacgagcggggagacggaggcatctacattggctccatcatg
aagggtggggctgtggcggccgacgggcgcattgagccaggggacatgcttttgcaggtg
aatgacatgaactttgagaacatgagcaatgatgacgccgtgcgggtgctgagggacatt
gtgcacaagcctggccccattgtgctgactgtggccaagtgctgggatccctctcctcag
gcctatttcactctcccccgaaatgagcccatccagccaattgaccctgctgcctgggtg
tcccattccgcggctctgactggcaccttcccagcctatccaggctcctcgtccatgagc
accattacatctggatcgtctttgcctgatggctgtgagggccggggtctctccatccat
acggacatggcatcggtgaccaaggccatggcagctccagagtctggactggaagtccgg
gaccgcatgtggctcaagatcaccatccctaatgcctttctgggctcggatgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgcaaatatgccagc
gggctgctcaaagcgggtctgatccgacacaccgtcaacaagatcaccttctctgagcag
tgctattacgtcttcggagacctcagtggtggctgtgagagctacctagtcaacctgtct
ctcaatgacaacgatggctccagtggggcctcagaccaggataccctggctcctttgcct
ggggccaccccttggcccctgctgcccactttctcctaccaataccctgccccacacccc
tacagcccgcagcctccaccctaccatgagctttcatcttacacctatggtgggggcagt
gccagcagccagcacagtgagggcagccggagcagtgggtcgacacggagtgacgggggg
gcagggcgcacggggaggcccgaagagcgggcccccgagtccaagtctggtagtggcagt
gagtccgagccctccagccgagggggcagccttcggcggggtggggaaccaagtgggact
agcgatgggggccctcctccatccagaggctcaactgggggtgccgctaatctccgagcc
cacccagggctccatccctatggaccgccccctggcatggccctcccctacaaccccatg
atggtggtcatgatgcccccacctccacctccagtccctccagcagtgcagcctccgggg
gcccctccagtcagagacctgggctctgtgcccccagaactgacagccagccgccaaagc
ttccacatggccatgggcaatcccagcgagttctttgtggatgttatgtag
Nomascus leucogenys (northern white-cheeked gibbon): 100593186
Help
Entry
100593186 CDS
T03265
Symbol
DVL1
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-1 isoform X1
KO
K02353
segment polarity protein dishevelled
Organism
nle
Nomascus leucogenys (northern white-cheeked gibbon)
Pathway
nle04150
mTOR signaling pathway
nle04310
Wnt signaling pathway
nle04330
Notch signaling pathway
nle04390
Hippo signaling pathway
nle04550
Signaling pathways regulating pluripotency of stem cells
nle04916
Melanogenesis
nle04934
Cushing syndrome
nle05010
Alzheimer disease
nle05022
Pathways of neurodegeneration - multiple diseases
nle05165
Human papillomavirus infection
nle05200
Pathways in cancer
nle05217
Basal cell carcinoma
nle05224
Breast cancer
nle05225
Hepatocellular carcinoma
nle05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
nle00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100593186 (DVL1)
04330 Notch signaling pathway
100593186 (DVL1)
04390 Hippo signaling pathway
100593186 (DVL1)
04150 mTOR signaling pathway
100593186 (DVL1)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100593186 (DVL1)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100593186 (DVL1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100593186 (DVL1)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100593186 (DVL1)
05226 Gastric cancer
100593186 (DVL1)
05217 Basal cell carcinoma
100593186 (DVL1)
05224 Breast cancer
100593186 (DVL1)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100593186 (DVL1)
09164 Neurodegenerative disease
05010 Alzheimer disease
100593186 (DVL1)
05022 Pathways of neurodegeneration - multiple diseases
100593186 (DVL1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100593186 (DVL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
PDZ
DEP
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
100593186
NCBI-ProteinID:
XP_030661777
Ensembl:
ENSNLEG00000000028
LinkDB
All DBs
Position
24:complement(2445369..2459070)
Genome browser
AA seq
695 aa
AA seq
DB search
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGVVK
EEIFDDNAKLPCFNGRVVSWLVLAEGAHSDVGSQGTDSHTDLPPPLERTGGIGDSRPPSF
HPNVASSRDGMDNETGTESMVSHRRERARRRNREEAARTNGHPRGDRRRDVGLPPDSAST
ALSSELESSSFVDSDEDGSTSRLSSSTEQSTSSRLIRKHKRRRRKQRLRQTDRASSFSSI
TDSTMSLNIVTVTLNMERHHFLGISIVGQSNDRGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDVNFENMSNDDAVRVLREIVSQTGPISLTVAKCWDPTPRSYFTVPRADPVRPIDP
AAWLSHTAALTGALPRYGTSPCSSAVTRTSSSSLTSSVPGAPQLEEAPLTVKSDMSAVVR
VMQLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFKERREARKYASSLLKHGFL
RHTVNKITFSEQCYYVFGDLCSNLATLNLNSGSSGASDQDTLAPLPHPAAPWPLGQGYPY
QYPGPPPCFPPAYQDPGFSYGSGSTGSQQSEGSKSSGSTRSSRRAPGREKERRAAGAGGS
GSESDHTAPSGVGSSWRERPAGQLSRGSSPRSQASATAPGLPPPHPMTKAYTVVGGPPGG
PPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq
2088 nt
NT seq
+upstream
nt +downstream
nt
atggcggagaccaagatcatctaccacatggacgaggaggagacgccgtacctggtcaag
ctgcccgtggcccccgagcgcgtcacgctagccgacttcaagaacgtgctcagcaaccgg
cccgtgcacgcctacaaattcttctttaagtccatggaccaggacttcggggtggtgaag
gaggagatctttgatgacaacgccaagcttccctgcttcaacggccgcgtggtctcctgg
ctggtcctggctgagggtgctcactcagatgtggggtcccagggcacggacagccacaca
gacctgcccccgcctctcgagcggacaggcggcatcggagactcccggcccccctccttc
cacccgaatgtggccagcagccgtgacgggatggacaatgagacaggcacggagtccatg
gtcagccaccggcgggagcgtgcccgacgccggaaccgcgaggaggccgcccggaccaat
gggcacccaaggggagaccgacggcgggatgtagggctgcccccagacagtgcgtccacc
gccctgagcagcgagcttgaatccagcagctttgtggactcggacgaggatggcagcaca
agcaggctgagcagctccacggagcagagcacctcatccaggctcatccggaagcacaaa
cgccggcggaggaagcagcgccttcggcagacggaccgggcctcctccttcagcagcata
accgactccaccatgtctctcaacatcgtcactgtcacgctcaacatggagagacatcac
tttctgggcatcagcatcgtggggcagagcaacgaccgtggagacggcggcatctacatc
ggctccatcatgaagggcggggctgtggccgctgacggccgcatcgagcccggcgacatg
ttgctgcaggtgaatgacgtgaactttgagaatatgagcaacgatgacgctgtgcgggtg
ctgcgggagatcgtgtcccagacggggcccatcagcctcactgtggccaagtgctgggac
ccgacgccccgaagctacttcaccgtcccacgggctgacccggtgcggcccatcgacccc
gccgcctggctgtcccacacggcggcactgacaggagccctgccccgctacggtacgagc
ccctgctccagcgccgtcacgcgcaccagctcctcctcactaaccagctccgtgcctggt
gctccacagctggaagaggcgccgctgacggtgaagagtgacatgagcgccgtggtccgg
gtcatgcagctgccagactcgggactggagatccgcgaccgtatgtggctcaagatcacc
attgccaacgctgtcatcggggcggacgtggtggactggctgtacacacacgtggaaggc
ttcaaggagcggcgggaggcccggaagtacgccagcagcttgctgaaacacggctttctg
cggcacacggtcaacaagatcaccttctccgagcagtgctactacgtattcggggacctc
tgcagcaatctcgccaccctgaacctcaacagtggctccagtggggcttcggatcaggac
acgctggccccgctgccccacccggctgccccctggcccctgggtcagggctacccctac
cagtacccggggcccccgccctgcttcccgcctgcctaccaggacccaggctttagctat
ggcagtggcagcaccgggagtcagcagagtgaagggagcaagagcagcgggtccacccgg
agcagccgccgggccccgggccgtgagaaggagcgtcgggcggcgggagccgggggcagt
ggcagtgaatcggatcacacggcaccgagtggggtggggagcagctggcgagagcgtccg
gctggccagctcagccgcggcagcagcccacgcagtcaggcctcggccaccgccccgggg
ctccccccgccccaccccatgaccaaggcctatacggtggtgggggggccccccggggga
ccccctgtccgggagctggctgccgtccccccggagttgacaggcagtcgccagtccttt
cagaaggctatggggaacccctgtgagttcttcgtggacatcatgtga
DBGET
integrated database retrieval system
