Homo sapiens (human): 1855
Help
Entry
1855 CDS
T01001
Symbol
DVL1, DRS2, DVL, DVL1L1, DVL1P1
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-1 isoform 1
KO
K02353
segment polarity protein dishevelled
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04330
Notch signaling pathway
hsa04390
Hippo signaling pathway
hsa04519
Cadherin signaling
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
hsa04934
Cushing syndrome
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
hsa05200
Pathways in cancer
hsa05217
Basal cell carcinoma
hsa05224
Breast cancer
hsa05225
Hepatocellular carcinoma
hsa05226
Gastric cancer
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06215
WNT signaling (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06263
Hepatocellular carcinoma
nt06270
Breast cancer
nt06271
Endometrial cancer
nt06274
Thyroid cancer
nt06505
WNT signaling
nt06549
Cadherin signaling
Element
N00056
Wnt signaling pathway, Canonical pathway
N00059
FZD7-overexpression to Wnt signaling pathway
N00060
LRP6-overexpression to Wnt signaling pathway
N01427
WNT5A-ROR signaling pathway
N01444
NXN mutation to WNT5A-ROR signaling pathway
N02010
Wnt signaling pathway, PCP pathway
Disease
H00485
Robinow syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
1855 (DVL1)
04330 Notch signaling pathway
1855 (DVL1)
04390 Hippo signaling pathway
1855 (DVL1)
04150 mTOR signaling pathway
1855 (DVL1)
09133 Signaling molecules and interaction
04519 Cadherin signaling
1855 (DVL1)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
1855 (DVL1)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
1855 (DVL1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
1855 (DVL1)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
1855 (DVL1)
05226 Gastric cancer
1855 (DVL1)
05217 Basal cell carcinoma
1855 (DVL1)
05224 Breast cancer
1855 (DVL1)
09172 Infectious disease: viral
05165 Human papillomavirus infection
1855 (DVL1)
09164 Neurodegenerative disease
05010 Alzheimer disease
1855 (DVL1)
05022 Pathways of neurodegeneration - multiple diseases
1855 (DVL1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
1855 (DVL1)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
PDZ
DEP
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
1855
NCBI-ProteinID:
NP_001317240
OMIM:
601365
HGNC:
3084
Ensembl:
ENSP00000368166.5
UniProt:
O14640
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(1335278..1349418)
Genome browser
AA seq
695 aa
AA seq
DB search
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGVVK
EEIFDDNAKLPCFNGRVVSWLVLAEGAHSDAGSQGTDSHTDLPPPLERTGGIGDSRPPSF
HPNVASSRDGMDNETGTESMVSHRRERARRRNREEAARTNGHPRGDRRRDVGLPPDSAST
ALSSELESSSFVDSDEDGSTSRLSSSTEQSTSSRLIRKHKRRRRKQRLRQADRASSFSSI
TDSTMSLNIVTVTLNMERHHFLGISIVGQSNDRGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDVNFENMSNDDAVRVLREIVSQTGPISLTVAKCWDPTPRSYFTVPRADPVRPIDP
AAWLSHTAALTGALPRYGTSPCSSAVTRTSSSSLTSSVPGAPQLEEAPLTVKSDMSAVVR
VMQLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFKERREARKYASSLLKHGFL
RHTVNKITFSEQCYYVFGDLCSNLATLNLNSGSSGTSDQDTLAPLPHPAAPWPLGQGYPY
QYPGPPPCFPPAYQDPGFSYGSGSTGSQQSEGSKSSGSTRSSRRAPGREKERRAAGAGGS
GSESDHTAPSGVGSSWRERPAGQLSRGSSPRSQASATAPGLPPPHPTTKAYTVVGGPPGG
PPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq
2088 nt
NT seq
+upstream
nt +downstream
nt
atggcggagaccaagattatctaccacatggacgaggaggagacgccgtacctggtcaag
ctgcccgtggcccccgagcgcgtcacgctggccgacttcaagaacgtgctcagcaaccgg
cccgtgcacgcctacaaattcttctttaagtccatggaccaggacttcggggtggtgaag
gaggagatctttgatgacaatgccaagcttccctgcttcaacggccgcgtggtctcctgg
ctggtcctggctgagggtgctcactcggatgcggggtcccagggcacggacagccacaca
gacctgcccccgcctcttgagcggacaggcggcatcggggactcccggcccccctccttc
cacccaaatgtggccagcagccgtgacgggatggacaacgagacaggcacggagtccatg
gtcagtcaccggcgggagcgtgcccgacgccggaaccgcgaggaggccgcccggaccaat
gggcacccaaggggagaccgacggcgggatgtggggctgcccccagacagcgcgtccacc
gccctcagcagcgagcttgagtccagcagctttgtggactcggacgaggatggcagcacg
agcaggctcagcagctccacggagcagagcacctcatccagactcatccggaagcacaaa
cgccggcggaggaagcagcgccttcggcaggcggaccgggcctcctccttcagcagcata
accgactccaccatgtccctcaacatcgtcactgtcacgctcaacatggaaagacatcac
tttctgggcatcagcatcgtggggcagagcaacgaccgtggagacggcggcatctacatt
ggctccatcatgaagggcggggctgtggccgctgacggccgcatcgagcccggcgacatg
ttgctgcaggtgaatgacgtgaactttgagaacatgagcaatgacgatgccgtgcgggtg
ctgcgggagatcgtttcccagacggggcccatcagcctcactgtggccaagtgctgggac
ccaacgccccgaagctacttcaccgtcccacgggctgacccggtgcggcccatcgacccc
gccgcctggctgtcccacacggcggcactgacaggagccctgccccgctacggtacgagt
ccctgctccagcgccgtcacgcgcaccagctcctcctcactaaccagctccgtgcctggt
gctccacagctggaagaggcgccgctgacggtgaagagtgacatgagcgccgtcgtccgg
gtcatgcagctgccagactcgggactggagatccgcgaccgcatgtggctcaagatcacc
atcgccaatgccgtcatcggggcggacgtggtggactggctgtacacacacgtggagggc
ttcaaggagcggcgggaggcccggaagtacgccagcagcttgctgaagcacggcttcctg
cggcacacggtcaacaagatcaccttctccgagcagtgctactacgtcttcggggatctc
tgcagcaatctcgccaccctgaacctcaacagtggctccagtgggacttcggatcaggac
acgctggccccgctgccccacccggctgccccctggcctctgggtcagggctacccctac
cagtacccgggacccccaccctgcttcccgcctgcctaccaggacccgggctttagctat
ggcagcggcagcaccgggagtcagcagagtgaagggagcaaaagcagtgggtccacccgg
agcagccgccgggccccgggccgtgagaaggagcgtcgggcggcgggagctgggggcagt
ggcagtgaatcggatcacacggcaccgagtggggtggggagcagctggcgagagcgtccg
gccggccagctcagccgtggcagcagcccacgcagtcaggcctcggctaccgccccgggg
ctccccccgccccaccccacgaccaaggcctatacagtggtgggggggccacccggggga
ccccctgtccgggagctggctgccgtccccccggaattgacaggcagccgccagtccttc
cagaaggctatggggaacccctgcgagttcttcgtggacatcatgtga
Homo sapiens (human): 1856
Help
Entry
1856 CDS
T01001
Symbol
DVL2
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-2
KO
K02353
segment polarity protein dishevelled
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04330
Notch signaling pathway
hsa04390
Hippo signaling pathway
hsa04519
Cadherin signaling
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
hsa04934
Cushing syndrome
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
hsa05200
Pathways in cancer
hsa05217
Basal cell carcinoma
hsa05224
Breast cancer
hsa05225
Hepatocellular carcinoma
hsa05226
Gastric cancer
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06215
WNT signaling (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06263
Hepatocellular carcinoma
nt06270
Breast cancer
nt06271
Endometrial cancer
nt06274
Thyroid cancer
nt06505
WNT signaling
nt06549
Cadherin signaling
Element
N00056
Wnt signaling pathway, Canonical pathway
N00059
FZD7-overexpression to Wnt signaling pathway
N00060
LRP6-overexpression to Wnt signaling pathway
N01427
WNT5A-ROR signaling pathway
N01444
NXN mutation to WNT5A-ROR signaling pathway
N02010
Wnt signaling pathway, PCP pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
1856 (DVL2)
04330 Notch signaling pathway
1856 (DVL2)
04390 Hippo signaling pathway
1856 (DVL2)
04150 mTOR signaling pathway
1856 (DVL2)
09133 Signaling molecules and interaction
04519 Cadherin signaling
1856 (DVL2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
1856 (DVL2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
1856 (DVL2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
1856 (DVL2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
1856 (DVL2)
05226 Gastric cancer
1856 (DVL2)
05217 Basal cell carcinoma
1856 (DVL2)
05224 Breast cancer
1856 (DVL2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
1856 (DVL2)
09164 Neurodegenerative disease
05010 Alzheimer disease
1856 (DVL2)
05022 Pathways of neurodegeneration - multiple diseases
1856 (DVL2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
1856 (DVL2)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
DEP
PDZ
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
1856
NCBI-ProteinID:
NP_004413
OMIM:
602151
HGNC:
3086
Ensembl:
ENSP00000005340.4
UniProt:
O14641
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:complement(7225342..7234517)
Genome browser
AA seq
736 aa
AA seq
DB search
MAGSSTGGGGVGETKVIYHLDEEETPYLVKIPVPAERITLGDFKSVLQRPAGAKYFFKSM
DQDFGVVKEEISDDNARLPCFNGRVVSWLVSSDNPQPEMAPPVHEPRAELAPPAPPLPPL
PPERTSGIGDSRPPSFHPNVSSSHENLEPETETESVVSLRRERPRRRDSSEHGAGGHRTG
GPSRLERHLAGYESSSTLMTSELESTSLGDSDEEDTMSRFSSSTEQSSASRLLKRHRRRR
KQRPPRLERTSSFSSVTDSTMSLNIITVTLNMEKYNFLGISIVGQSNERGDGGIYIGSIM
KGGAVAADGRIEPGDMLLQVNDMNFENMSNDDAVRVLRDIVHKPGPIVLTVAKCWDPSPQ
AYFTLPRNEPIQPIDPAAWVSHSAALTGTFPAYPGSSSMSTITSGSSLPDGCEGRGLSVH
TDMASVTKAMAAPESGLEVRDRMWLKITIPNAFLGSDVVDWLYHHVEGFPERREARKYAS
GLLKAGLIRHTVNKITFSEQCYYVFGDLSGGCESYLVNLSLNDNDGSSGASDQDTLAPLP
GATPWPLLPTFSYQYPAPHPYSPQPPPYHELSSYTYGGGSASSQHSEGSRSSGSTRSDGG
AGRTGRPEERAPESKSGSGSESEPSSRGGSLRRGGEASGTSDGGPPPSRGSTGGAPNLRA
HPGLHPYGPPPGMALPYNPMMVVMMPPPPPPVPPAVQPPGAPPVRDLGSVPPELTASRQS
FHMAMGNPSEFFVDVM
NT seq
2211 nt
NT seq
+upstream
nt +downstream
nt
atggcgggtagcagcactgggggcggtggggttggggagacgaaggtgatttaccacctg
gatgaggaagagactccctacctggtgaagatccctgtccccgccgagcgcatcaccctc
ggcgatttcaagagcgtcctgcagcggcccgcgggcgccaagtactttttcaagtctatg
gatcaggatttcggggtggtgaaggaagaaatttcagatgacaacgcccgcctcccctgc
ttcaacggaagggtggtatcctggctggtgtcctcagataatccccaacccgagatggcc
cctccagtccatgagcctcgggcagaactggcgcctccagccccacctttacctcctttg
ccacccgagaggaccagcggcattggggactcaaggcctccatccttccaccctaatgtg
tccagcagccatgagaatctggagcctgagacagaaaccgagtcagtagtgtcactgagg
cgggagcggcctcgcaggagagacagcagtgagcatggcgctgggggccacaggactggt
ggcccctcaaggctggagcgccacctggccggatacgagagctcctctaccctcatgacc
agcgagctggagagtaccagcctgggggactcggacgaggaggacaccatgagcaggttc
agcagctccacggagcagagcagtgcctcccgcctccttaagcgccaccggcggcgaagg
aagcagaggccaccccgcctggagaggacgtcatccttcagcagcgtcacagattccaca
atgtctctcaatatcatcacagtcacgctaaacatggagaagtacaacttcctgggtatc
tccattgttggccagagcaatgagcggggagacggaggcatctacattggctccatcatg
aagggtggggctgtggcggccgacgggcgcattgagccaggggacatgcttttgcaggtg
aatgacatgaactttgagaacatgagcaacgatgacgctgtgcgggtgctgagggacatt
gtgcacaagcctggccccattgtgctgactgtggccaagtgctgggatccctctcctcag
gcctatttcactctcccccgaaatgagcccatccagccaattgaccctgctgcctgggtg
tcccattccgcggctctgactggcaccttcccagcctatccaggttcctcctccatgagc
accattacatctggatcgtctttgcctgatggctgtgaaggccggggtctctccgtccat
acggacatggcatcggtgaccaaggccatggcagctccagagtctggactggaagtccgg
gaccgcatgtggctcaagatcaccatccctaatgcctttctgggctcggatgtggttgac
tggctctaccatcacgtggagggctttcctgagcggcgggaggcccgcaagtatgccagc
gggctgctcaaagcaggcctgatccgacacaccgtcaacaagatcaccttctctgagcag
tgctattacgtcttcggagacctcagtggtggctgtgagagctacctagtcaacctgtct
ctcaatgacaacgatggctccagtggggcttcagaccaggataccctggctcctctgcct
ggggccaccccctggcccctgctgcccactttctcctaccaataccctgccccacacccc
tacagcccgcagcctccaccctaccatgagctttcatcttacacctatggtgggggcagt
gccagcagccagcatagtgagggcagccggagcagtgggtcgacacggagtgatgggggg
gcagggcgcacggggaggcccgaggagcgggcccccgagtccaagtccggcagtggcagt
gagtctgagccctccagccgagggggcagccttcggcggggtggggaagcaagtgggact
agcgatgggggccctcctccatccagaggctcaactgggggtgcccctaatctccgagcc
cacccagggctccatccctatggaccgccccctggcatggccctcccctacaaccccatg
atggtggtcatgatgcccccacctccacctccagtccctccagcagtgcagcctccgggg
gcccctccagtcagagacctgggctctgtgcccccagaactgacagccagccgccaaagc
ttccacatggccatgggcaatcccagcgagttctttgtggatgttatgtag
Homo sapiens (human): 1857
Help
Entry
1857 CDS
T01001
Symbol
DVL3, DRS3
Name
(RefSeq) segment polarity protein dishevelled homolog DVL-3
KO
K02353
segment polarity protein dishevelled
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04330
Notch signaling pathway
hsa04390
Hippo signaling pathway
hsa04519
Cadherin signaling
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
hsa04934
Cushing syndrome
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
hsa05200
Pathways in cancer
hsa05217
Basal cell carcinoma
hsa05224
Breast cancer
hsa05225
Hepatocellular carcinoma
hsa05226
Gastric cancer
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06215
WNT signaling (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06263
Hepatocellular carcinoma
nt06270
Breast cancer
nt06271
Endometrial cancer
nt06274
Thyroid cancer
nt06505
WNT signaling
nt06549
Cadherin signaling
Element
N00056
Wnt signaling pathway, Canonical pathway
N00059
FZD7-overexpression to Wnt signaling pathway
N00060
LRP6-overexpression to Wnt signaling pathway
N01427
WNT5A-ROR signaling pathway
N01444
NXN mutation to WNT5A-ROR signaling pathway
N02010
Wnt signaling pathway, PCP pathway
Disease
H00485
Robinow syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
1857 (DVL3)
04330 Notch signaling pathway
1857 (DVL3)
04390 Hippo signaling pathway
1857 (DVL3)
04150 mTOR signaling pathway
1857 (DVL3)
09133 Signaling molecules and interaction
04519 Cadherin signaling
1857 (DVL3)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
1857 (DVL3)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
1857 (DVL3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
1857 (DVL3)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
1857 (DVL3)
05226 Gastric cancer
1857 (DVL3)
05217 Basal cell carcinoma
1857 (DVL3)
05224 Breast cancer
1857 (DVL3)
09172 Infectious disease: viral
05165 Human papillomavirus infection
1857 (DVL3)
09164 Neurodegenerative disease
05010 Alzheimer disease
1857 (DVL3)
05022 Pathways of neurodegeneration - multiple diseases
1857 (DVL3)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
1857 (DVL3)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
DEP
PDZ
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
1857
NCBI-ProteinID:
NP_004414
OMIM:
601368
HGNC:
3087
Ensembl:
ENSP00000316054.3
UniProt:
Q92997
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:184155377..184173614
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
ctgcccctgcccgccgagcgcgtcaccttggcggactttaagggcgttttgcagcgaccc
agctataagttcttcttcaagtctatggacgacgatttcggagtggtgaaggaggagatc
tcggatgacaatgccaagctaccatgcttcaatggccgggtggtgtcctggctggtgtca
gctgagggctcacacccagacccagcccccttctgtgctgataacccatcggagctgcca
ccacctatggagcgcacgggaggcatcggggactcccgacccccatccttccaccctcat
gctggtgggggcagccaggagaacctggacaatgacacagagacggactctttggtgtct
gcccagcgagagcggccacgccggagggatggcccagagcatgcaacccggctaaatgga
actgcgaagggggaacggcggcgagaaccagggggttatgatagctcatccacccttatg
agcagtgagctggagaccaccagcttctttgactcagatgaggatgactccaccagcagg
ttcagcagctccacagaacagagcagtgcctcacgcctgatgagaagacacaagcggcgg
cggcggaagcagaaggtttctcggattgagcggtcctcgtccttcagcagcatcacggac
tccaccatgtcactcaacatcatcacggtcactctcaacatggaaaaatataacttcttg
ggcatctccattgtgggccaaagcaacgagcgtggtgacggcggcatctacattggctct
atcatgaagggtggggccgtggctgctgatggacgcatcgagccaggagatatgttgtta
caggtaaacgagatcaactttgagaacatgagtaatgacgatgcagtccgggtactgcgg
gagattgtgcacaaaccggggcccatcaccctgactgtagccaagtgctgggacccaagt
ccacgtggttgcttcacattgcccaggagcgagcccatccggcccattgaccctgcggcc
tgggtctcccacactgcagccatgaccggcaccttccctgcatacggcatgagcccctcc
ctgagcaccatcacctccaccagctcctccatcaccagttccatccctgacacagagcgc
ctagacgacttccacttgtccatccacagtgacatggctgccatcgtaaaagccatggcc
tcccctgaatcagggttggaggtccgtgaccgcatgtggctcaagattaccatccctaat
gctttcatcggctcagatgtggtggactggctgtaccacaatgtggaaggcttcacggac
cggagggaggcccgcaagtatgccagcaacctgctgaaagctggcttcatccgccatacc
gtcaacaagatcaccttctccgagcagtgctactacatcttcggtgacctctgcggcaac
atggccaacctgtctctccacgatcacgatggctccagtggcgcctctgaccaggacaca
ctggcccctttgccgcacccgggggccgccccttggcccatggctttcccgtaccagtac
ccgccacccccgcacccatacaacccgcacccgggcttcccggagctgggctacagctac
ggcgggggcagcgccagcagtcagcacagcgaaggcagtcggagcagtggctccaaccgt
agcggcagcgatcggaggaaggagaaggacccgaaggccggggactccaagtccgggggc
agcggcagcgaatcggaccacaccacacgcagcagcctgcgggggccgcgggagcgggcg
cccagcgagcgctcagggccggcggccagcgagcacagccaccgcagccaccattccctg
gccagcagccttcgcagccaccacacacacccgagctacggtcctcccggagtgccccct
ctctacggcccccccatgctgatgatgcccccgccgcccgcggccatggggcccccagga
gcccctccgggccgcgacctggcctcagtgcccccggaactgaccgccagcagacagtcc
ttccgcatggccatgggaaaccccagtgagttctttgtggatgtgatgtga
Homo sapiens (human): 22881
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Entry
22881 CDS
T01001
Symbol
ANKRD6
Name
(RefSeq) ankyrin repeat domain-containing protein 6 isoform a
KO
K21435
ankyrin repeat domain-containing protein 6
Organism
hsa
Homo sapiens (human)
Pathway
hsa04310
Wnt signaling pathway
hsa04519
Cadherin signaling
Network
nt06505
WNT signaling
nt06549
Cadherin signaling
Element
N02010
Wnt signaling pathway, PCP pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
22881 (ANKRD6)
09133 Signaling molecules and interaction
04519 Cadherin signaling
22881 (ANKRD6)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
22881 (ANKRD6)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Kinases and associated factors
Kinase associated protein
22881 (ANKRD6)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Ank
Ank_2
Ank_4
Ank_5
Ank_3
Ank_KRIT1
Apolipoprotein
DUF445
STB2_C
PRR11_2nd
Phasin
ANK_LRRK2
Motif
Other DBs
NCBI-GeneID:
22881
NCBI-ProteinID:
NP_001229738
OMIM:
610583
HGNC:
17280
Ensembl:
ENSP00000345767.4
UniProt:
Q9Y2G4
B7Z3D2
LinkDB
All DBs
Position
6:89433152..89633834
Genome browser
AA seq
727 aa
AA seq
DB search
MSQQDAVAALSERLLVAAYKGQTENVVQLINKGARVAVTKHGRTPLHLAANKGHLPVVQI
LLKAGCDLDVQDDGDQTALHRATVVGNTEIIAALIHEGCALDRQDKDGNTALHEASWHGF
SQSAKLLIKAGANVLAKNKAGNTALHLACQNSHSQSTRVLLLAGSRADLKNNAGDTCLHV
AARYNHLSIIRLLLTAFCSVHEKNQAGDTALHVAAALNHKKVAKILLEAGADTTIVNNAG
QTPLETARYHNNPEVALLLTKAPQVLRFSRGRSLRKKRERLKEERRAQSVPRDEVAQSKG
SVSAGDTPSSEQAVARKEEAREEFLSASPEPRAKDDRRRKSRPKVSAFSDPTPPADQQPG
HQKNLHAHNHPKKRNRHRCSSPPPPHEFRAYQLYTLYRGKDGKVMQAPINGCRCEPLINK
LENQLEATVEEIKAELGSVQDKMNTKLGQMENKTQHQMRVLDKLMVERLSAERTECLNRL
QQHSDTEKHEGEKRQISLVDELKTWCMLKIQNLEQKLSGDSRACRAKSTPSTCESSTGVD
QLVVTAGPAAASDSSPPVVRPKEKALNSTATQRLQQELSSSDCTGSRLRNVKVQTALLPM
NEAARSDQQAGPCVNRGTQTKKSGKSGPTRHRAQQPAASSTCGQPPPATGSEQTGPHIRD
TSQALELTQYFFEAVSTQMEKWYERKIEEARSQANQKAQQDKATLKEHIKSLEEELAKLR
TRVQKEN
NT seq
2184 nt
NT seq
+upstream
nt +downstream
nt
atgagccagcaagatgcggtcgctgcactttcagagcgccttctcgtagctgcgtacaaa
ggccaaacagagaatgtggttcagctcatcaacaagggcgccagggtagcggttaccaag
catggccggactcccctgcatcttgctgccaataagggccatcttcctgtggtccagatc
ttgctgaaggctggctgcgaccttgatgtccaggatgatggggaccagaccgccttgcac
cgggccacagtggtggggaacacggagatcatcgcggcgctcatccacgaagggtgtgcc
ctggacagacaagacaaggatgggaatacagccttgcatgaagcatcctggcatggtttc
agccagtcagccaagctgctcattaaagcaggagccaacgtgcttgccaagaacaaggcg
gggaacacagctctgcacctggcctgccagaacagccactcccagagcacgcgcgtcctc
ctgctggccgggtcccgcgctgacctcaaaaataatgcaggagacacctgtttgcacgtt
gctgcgcgctataatcacttgtccatcattaggctcctcctcactgctttctgttctgtc
catgaaaagaaccaggctggagacacagcacttcacgttgctgctgccctaaatcacaag
aaggtggccaaaatcttactggaagccggagcagatacgaccattgttaacaatgcaggc
cagactccgctggagactgcccgctaccacaataacccggaagttgctcttctccttact
aaagctccccaggtcttgcgcttcagtcgtgggcgaagcctgaggaaaaagagagagagg
ctcaaggaagagaggagagcccagtctgtgccaagagatgaggtggcccaaagcaagggc
agtgtctcagcaggagacacccccagcagtgaacaggctgtggccagaaaagaagaagcc
agagaagagttcctgtcagcctccccagaacccagagcaaaggatgacaggaggagaaag
tcaaggcccaaggtgtcagcattttctgaccccaccccaccagccgaccaacagcctgga
caccagaagaacctgcatgctcataatcaccctaaaaagaggaacaggcatcggtgttca
tccccacccccaccccatgagttcagggcgtatcagctctacacattgtaccggggcaag
gatgggaaagtgatgcaggcaccaataaatggttgtcgatgtgaacctctaatcaacaag
ctggagaatcagttggaggctactgtggaggagataaaagcagagctgggatcggttcag
gacaaaatgaatacaaagctggggcagatggagaataagacccagcaccaaatgcgtgtt
ttggacaagctgatggttgagcgactttctgcagagaggacggagtgcctgaaccgcctg
caacagcactcagacacagagaagcatgagggggagaaacgacagatatccttggtggat
gaattaaaaacctggtgcatgttaaagattcagaatctggagcagaagctttctggagat
tctagggcctgcagagctaaatccacaccatctacttgtgagtcctctacaggtgtggac
caattagtggtgactgcaggtccagcagcagcttccgacagctcccctccagtggttagg
cccaaagagaaggccctcaactccactgctacccagagactccagcaggagctgtcgtct
tctgactgtacaggctcccgactgagaaacgtcaaggtccagacagccttgctacccatg
aatgaggcagccagatctgatcagcaggctgggccctgcgtcaacagaggcactcaaact
aagaagtctgggaagagtgggccaacaaggcatcgtgcccagcaacccgcagccagcagc
acctgtgggcagccgccaccagccacaggcagcgagcagactggccctcacattcgggac
acctcccaagctctggagcttacccagtatttttttgaggctgtttctacccagatggaa
aagtggtatgaaaggaagattgaagaagcacgaagccaagccaatcagaaagcccagcaa
gataaggctacattgaaggaacacattaaaagtttagaagaggaacttgccaaactaagg
actagggtgcagaaggaaaattag
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