Piliocolobus tephrosceles (Ugandan red Colobus): 111521282
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Entry
111521282 CDS
T07491
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2
KO
K02353
segment polarity protein dishevelled
Organism
pteh
Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04150
mTOR signaling pathway
pteh04310
Wnt signaling pathway
pteh04330
Notch signaling pathway
pteh04390
Hippo signaling pathway
pteh04550
Signaling pathways regulating pluripotency of stem cells
pteh04916
Melanogenesis
pteh04934
Cushing syndrome
pteh05010
Alzheimer disease
pteh05022
Pathways of neurodegeneration - multiple diseases
pteh05165
Human papillomavirus infection
pteh05200
Pathways in cancer
pteh05217
Basal cell carcinoma
pteh05224
Breast cancer
pteh05225
Hepatocellular carcinoma
pteh05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pteh00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
111521282 (DVL2)
04330 Notch signaling pathway
111521282 (DVL2)
04390 Hippo signaling pathway
111521282 (DVL2)
04150 mTOR signaling pathway
111521282 (DVL2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
111521282 (DVL2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
111521282 (DVL2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
111521282 (DVL2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
111521282 (DVL2)
05226 Gastric cancer
111521282 (DVL2)
05217 Basal cell carcinoma
111521282 (DVL2)
05224 Breast cancer
111521282 (DVL2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
111521282 (DVL2)
09164 Neurodegenerative disease
05010 Alzheimer disease
111521282 (DVL2)
05022 Pathways of neurodegeneration - multiple diseases
111521282 (DVL2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
111521282 (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:
111521282
NCBI-ProteinID:
XP_023040338
Ensembl:
ENSPTEG00000016198
UniProt:
A0A8C9HCK6
LinkDB
All DBs
Position
16:complement(7007965..7017255)
Genome browser
AA seq
736 aa
AA seq
DB search
MAGSIAGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMTPPAHEPRAELAPPAPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERPRRRDSSEHGAGGHRTG
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEEDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSIH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTFGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEPSGTGDGGPPPSRGSTGGAPNLRA
HSGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq
2211 nt
NT seq
+upstream
nt +downstream
nt
atggcgggcagcatcgctgggggcggtggggttggggagacgaaggtgatttaccacctg
gatgaggaagagactccatacctggtgaagatccctgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgtcctgcagcggcccgcgggcgccaagtactttttcaagtctatg
gatcaggatttcggagtggtgaaggaagaaatttcagatgacaacgcccgcctcccctgc
ttcaacggaagggtggtatcctggctggtgtcctcagataatccccaaccggagatgact
cccccagcccacgagcctcgggcagaactggcacctccagccccacctttaccccctttg
ccacccgagaggaccagcggcattggggactcaaggcctccctcctttcaccctaatgtg
tccagcagccatgagaatctggagcctgagacagaaaccgagtcagtagtgtcactgaga
cgggagcggcctcgcaggagagacagcagtgagcatggcgctgggggccacaggactggt
ggcccctcaaggctggagcgccacctggccggatatgagagctcctctaccctcatgacc
agtgagctggagagtaccagcctgggggactcggacgaggaggacaccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctccttaagcgccaccgacggcggagg
aagcagcggccaccccgcctggagaggacatcgtccttcagcagcgtcacagattccacc
atgtctctcaatatcatcacagtcacgctaaacatggagaagtacaacttcctgggtatc
tccattgtgggccaaagcaatgagcggggagacggaggcatctacattggctccatcatg
aagggtggggctgtggcggccgacgggcgcattgagccaggggacatgcttttgcaggtg
aatgacatgaactttgagaacatgagcaatgacgacgccgtgcgggtgctgagggacatc
gtgcacaagcctggccccattgtgctgactgtggccaagtgctgggatccctctcctcag
gcctatttcactctccctcgaaatgagcccatccagccaattgaccctgctgcctgggtg
tcccactctgcggctctgactggcaccttcccagcctatccgggctcctcctccatgagc
accattacatctggatcctctttgcctgatggctgtgagggccggggtctctccatccat
acggacatggcatcggtgaccaaggccatggcagctccagagtctggactggaagtccgg
gaccgcatgtggctcaagatcaccatccctaatgcctttctgggctcggatgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgcaagtatgccagc
gggctgctcaaagccggcctgatccgacacaccgtcaacaagatcaccttctctgagcag
tgctattacgtcttcggagacctcagtggtggctgtgagagctacctagtcaacctgtct
ctcaatgacaacgatggctccagtggggcttcggaccaggataccctggctcctctgccg
ggggccaccccctggcccttgctgcccactttctcctaccaatacccggccccacacccc
tacagcccgcagcccccaccctaccatgaactttcatcttatacctttggtgggggcagt
gccagcagccagcacagtgagggcagccggagcagtgggtcgacacggagtgacgggggg
gcagggcgcacagggaggcccgaggagcgggcccccgagtccaagtccggcagtggcagt
gagtccgagccctccagccgagggggcagccttcggcggggtggggaaccaagtgggact
ggcgatgggggccctcctccatccagaggctcaactgggggtgcccctaatctccgagcc
cactcggggctccatccctatggaccaccccctggcatggccctcccctacaaccccatg
atggtggtcatgatgcccccacccccacctccagtccctccagcagtgcagcctccgggg
gcccctccagtcagagacctgggctccgtgccgccagaactgacagccagccgccaaagc
ttccacatggccatgggcaatcccagcgagttctttgtggatgttatgtag
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