KEGG   ORTHOLOGY: K00572Help
Entry
K00572                      KO                                     

Name
WNT7
Definition
wingless-type MMTV integration site family, member 7
Pathway
ko04150  mTOR signaling pathway
ko04310  Wnt signaling pathway
ko04390  Hippo signaling pathway
ko04550  Signaling pathways regulating pluripotency of stem cells
ko04916  Melanogenesis
ko04934  Cushing syndrome
ko05165  Human papillomavirus infection
ko05200  Pathways in cancer
ko05205  Proteoglycans in cancer
ko05217  Basal cell carcinoma
ko05224  Breast cancer
ko05225  Hepatocellular carcinoma
ko05226  Gastric cancer
Disease
H00846  Fuhrmann syndrome
H00847  Al-Awadi/Raas-Rothschild syndrome
Brite
KEGG Orthology (KO) [BR:ko00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    K00572  WNT7; wingless-type MMTV integration site family, member 7
   04390 Hippo signaling pathway
    K00572  WNT7; wingless-type MMTV integration site family, member 7
   04150 mTOR signaling pathway
    K00572  WNT7; wingless-type MMTV integration site family, member 7
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    K00572  WNT7; wingless-type MMTV integration site family, member 7
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    K00572  WNT7; wingless-type MMTV integration site family, member 7
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    K00572  WNT7; wingless-type MMTV integration site family, member 7
   05205 Proteoglycans in cancer
    K00572  WNT7; wingless-type MMTV integration site family, member 7
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    K00572  WNT7; wingless-type MMTV integration site family, member 7
   05226 Gastric cancer
    K00572  WNT7; wingless-type MMTV integration site family, member 7
   05217 Basal cell carcinoma
    K00572  WNT7; wingless-type MMTV integration site family, member 7
   05224 Breast cancer
    K00572  WNT7; wingless-type MMTV integration site family, member 7
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    K00572  WNT7; wingless-type MMTV integration site family, member 7
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    K00572  WNT7; wingless-type MMTV integration site family, member 7
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins
    K00572  WNT7; wingless-type MMTV integration site family, member 7
Glycosaminoglycan binding proteins [BR:ko00536]
 Heparan sulfate/Haparin
  Morphogens
   K00572  WNT7; wingless-type MMTV integration site family, member 7
BRITE hierarchy
Genes
HSA: 7476(WNT7A) 7477(WNT7B)
PTR: 104003805(WNT7B) 749914(WNT7A)
PPS: 100977315(WNT7B) 100995012(WNT7A)
GGO: 101146237(WNT7A)
PON: 100441147(WNT7A) 100451196(WNT7B)
NLE: 100579580(WNT7B) 100593900(WNT7A)
MCC: 693419(WNT7A) 713864(WNT7B)
MCF: 102135636(WNT7B) 102137321(WNT7A)
CSAB: 103223483(WNT7B) 103228043(WNT7A)
RRO: 104676099(WNT7B) 104679020(WNT7A)
RBB: 108514489(WNT7B) 108544845(WNT7A)
CJC: 100387909(WNT7A) 100414221(WNT7B)
MMU: 22421(Wnt7a) 22422(Wnt7b)
MCAL: 110296669(Wnt7a) 110310689(Wnt7b)
MPAH: 110316305(Wnt7a) 110335001(Wnt7b)
RNO: 114850(Wnt7a) 315196(Wnt7b)
MUN: 110545047(Wnt7b) 110549843(Wnt7a)
CGE: 100755799(Wnt7b) 100772978(Wnt7a)
NGI: 103730373(Wnt7a) 103743417(Wnt7b)
HGL: 101725735(Wnt7a) 101726616(Wnt7b)
OCU: 100355697(WNT7A) 103347432
TUP: 102484353(WNT7A) 102500004(WNT7B)
CFA: 481206(WNT7B) 607180(WNT7A)
VVP: 112914456(WNT7A) 112935842(WNT7B)
AML: 100474982(WNT7B) 100475153(WNT7A)
UMR: 103669629(WNT7A) 103674134(WNT7B)
UAH: 113241648(WNT7B) 113257229(WNT7A)
ORO: 101381717(WNT7A) 101386348(WNT7B)
FCA: 101083664(WNT7A) 101095592(WNT7B)
PTG: 102972888(WNT7A) 107180716(WNT7B)
AJU: 106978815(WNT7A) 113602684(WNT7B)
BTA: 100337066(WNT7B) 533782(WNT7A)
BIU: 109558644(WNT7B) 109576501(WNT7A)
BBUB: 102399122(WNT7A) 102401643(WNT7B)
PHD: 102324829(WNT7B) 102336785(WNT7A)
CHX: 102171665(WNT7A) 102176768(WNT7B)
OAS: 101109531(WNT7B) 114109341(WNT7A)
SSC: 100153445(WNT7A) 100626947(WNT7B)
CFR: 102506800(WNT7A) 102519277(WNT7B)
CDK: 105091978(WNT7B) 105093166(WNT7A)
LVE: 103068582(WNT7A) 103083305(WNT7B)
OOR: 101278865(WNT7A) 101282844(WNT7B)
DLE: 111168811(WNT7A) 111186418(WNT7B)
ECB: 100053027(WNT7B) 100055450(WNT7A)
EPZ: 103556791(WNT7A) 103558099(WNT7B)
EAI: 106829376(WNT7A) 106845973(WNT7B)
MYB: 102249626(WNT7A) 102257706(WNT7B)
MYD: 102758002 102774695(WNT7A)
MNA: 107534839(WNT7B) 107537987(WNT7A)
HAI: 109387605(WNT7B) 109390460(WNT7A)
RSS: 109451217(WNT7B) 109459247(WNT7A)
DRO: 112320683(WNT7A) 112322077(WNT7B)
PALE: 102888597(WNT7A) 102898026(WNT7B)
LAV: 100660629(WNT7B) 100675463(WNT7A)
MDO: 100014091(WNT7B)
SHR: 100925362(WNT7B) 100931119(WNT7A)
PCW: 110201658(WNT7B) 110204974(WNT7A)
OAA: 100075994(WNT7A) 100093588(WNT7B)
GGA: 374168(WNT7A) 427937(WNT7B)
MGP: 100542203(WNT7B) 100542958(WNT7A)
CJO: 107317577(WNT7B) 107319707(WNT7A)
APLA: 101792761(WNT7A) 101805245(WNT7B)
ACYG: 106038211(WNT7B) 106040033(WNT7A)
TGU: 100220226(WNT7B) 100220584(WNT7A)
LSR: 110470371(WNT7B) 110479430(WNT7A)
SCAN: 103816927(WNT7A) 103820439(WNT7B)
GFR: 102043987(WNT7A) 102044794(WNT7B)
FAB: 101813299(WNT7A) 101816884(WNT7B)
PHI: 102113507(WNT7B) 102113528(WNT7A)
PMAJ: 107204452(WNT7B) 107210469(WNT7A)
CCAE: 111923341(WNT7B) 111935250(WNT7A)
CCW: 104695759(WNT7A) 104696093(WNT7B)
ETL: 114067661(WNT7A) 114068280
FPG: 101913212(WNT7A) 101919373(WNT7B)
FCH: 102050340(WNT7B) 102056992(WNT7A)
CLV: 102084979(WNT7B) 102088082
EGZ: 104124300(WNT7A) 104135171(WNT7B)
NNI: 104012662(WNT7B) 104022169(WNT7A)
ACUN: 113475861(WNT7B) 113484979(WNT7A)
AAM: 106488582(WNT7A) 106488789(WNT7B)
AMJ: 102568312(WNT7B) 102575772(WNT7A)
PSS: 102450567(WNT7B) 102452569(WNT7A)
CMY: 102942821(WNT7B) 102945035(WNT7A)
CPIC: 101934994(WNT7B) 101939685(WNT7A)
ACS: 100553258(wnt7a) 100567981(wnt7b)
PVT: 110075003(WNT7B) 110081630(WNT7A)
PBI: 103052813(WNT7A) 103058473 103059073(WNT7B)
GJA: 107114761(WNT7B) 107118817(WNT7A)
XTR: 100145124(wnt7b) 100490426(wnt7c) 105947033
DRE: 100148840(wnt7bb) 563427(wnt7ba) 565714(wnt7aa)
AMEX: 103026929 103027182(wnt7a) 103028473(wnt7b) 103046044
TRU: 101071438(wnt7b) 101078823(wnt7a)
NCC: 104955515 104966327(wnt7b) 104966749(wnt7a)
CMK: 103179433(wnt7b) 103185034(wnt7a)
BFO: BRAFLDRAFT_56634(AmphiWnt7b)
CIN: 778938
SPU: 581981
SKO: 100313764(Wnt7)
DER: 6542264
DPE: 6592209
DSI: Dsimw501_GD10659(Dsim_GD10659)
DWI: 6640767
DAZ: 108615928
DNV: 108653824
DHE: 111604601
MDE: 101889017
AAG: 5570378
AME: 411919
BIM: 100741405
BTER: 100646705
SOC: 105193029
MPHA: 105833587
ACEP: 105618028
PBAR: 105432993
HST: 105181239
DQU: 106741954
CFO: 105259313
LHU: 105673358
PGC: 109853360
OBO: 105283919
PCF: 106791180
NVI: 100122745
MDL: 103580558
TCA: 661936(Wnt7)
DPA: 109536345
NVL: 108562837
BMOR: 101740841
PMAC: 106713271
PRAP: 110995122
HAW: 110382331
TNL: 113506522
DNX: 107166553
AGS: 114124781
CLEC: 106671019
FCD: 110845687
DPX: DAPPUDRAFT_64642(WNT7)
DPTE: 113789916
PCAN: 112571885
CRG: 105337729
MYI: 110441939
LAK: 106162452
SHX: MS3_06044
AQU: 100616534(WntB)
 » show all
TaxonomyKoalaUniProt
Reference
PMID:9161407
  Authors
Bui TD, Lako M, Lejeune S, Curtis AR, Strachan T, Lindsay S, Harris AL
  Title
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25.
  Journal
Gene 189:25-9 (1997)
DOI:10.1016/S0378-1119(96)00808-6
  Sequence
[hsa:7476]
Reference
  Authors
Kirikoshi H, Sekihara H, Katoh M
  Title
Molecular cloning and characterization of human WNT7B.
  Journal
Int J Oncol 19:779-83 (2001)
DOI:10.3892/ijo.19.4.779
  Sequence
[hsa:7477]
Reference
PMID:9790192
  Authors
Parr BA, McMahon AP
  Title
Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a.
  Journal
Nature 395:707-10 (1998)
DOI:10.1038/27221
  Sequence
[mmu:22421]

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