KEGG   ORTHOLOGY: K00572Help
Entry
K00572                      KO                                     

Name
WNT7
Definition
wingless-type MMTV integration site family, member 7
Pathway
mTOR signaling pathway
Wnt signaling pathway
Hippo signaling pathway
Signaling pathways regulating pluripotency of stem cells
Melanogenesis
HTLV-I infection
Pathways in cancer
Proteoglycans in cancer
Basal cell carcinoma
Breast cancer
Module
M00677  
Wnt signaling
Disease
H00846  
Fuhrmann syndrome
H00847  
Al-Awadi/Raas-Rothschild syndrome
Brite
KEGG Orthology (KO) [BR:ko00001]
 Environmental Information Processing
  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
 Cellular Processes
  Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    K00572  WNT7; wingless-type MMTV integration site family, member 7
 Organismal Systems
  Endocrine system
   04916 Melanogenesis
    K00572  WNT7; wingless-type MMTV integration site family, member 7
 Human Diseases
  Cancers
   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
   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
  Infectious diseases
   05166 HTLV-I infection
    K00572  WNT7; wingless-type MMTV integration site family, member 7
KEGG modules [BR:ko00002]
 Functional set
  Cellular processes
   Cell signaling
    M00677  Wnt signaling
     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: 
PON: 
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)
CJC: 
100387909(WNT7A) 100414221(WNT7B)
SBQ: 
MMU: 
22421(Wnt7a) 22422(Wnt7b)
RNO: 
114850(Wnt7a) 315196(Wnt7b)
CGE: 
100755799(Wnt7b) 100772978(Wnt7a)
NGI: 
103730373(Wnt7a) 103743417(Wnt7b)
HGL: 
101725735(Wnt7a) 101726616(Wnt7b)
OCU: 
TUP: 
102484353(WNT7A) 102500004(WNT7B)
CFA: 
481206(WNT7B) 607180(WNT7A)
AML: 
100474982(WNT7B) 100475153(WNT7A)
UMR: 
103669629(WNT7A) 103674134(WNT7B)
FCA: 
101083664(WNT7A) 101095592(WNT7B)
PTG: 
102972888(WNT7A) 107180716(WNT7B)
BTA: 
BOM: 
PHD: 
102324829(WNT7B) 102336785(WNT7A)
CHX: 
102171665(WNT7A) 102176768(WNT7B)
OAS: 
101109531(WNT7B)
SSC: 
100153445(WNT7A) 100626947(WNT7B)
CFR: 
102506800(WNT7A) 102519277(WNT7B)
BACU: 
LVE: 
103068582(WNT7A) 103083305(WNT7B)
ECB: 
100053027(WNT7B) 100055450(WNT7A)
MYB: 
102249626(WNT7A) 102257706(WNT7B)
MYD: 
PALE: 
102888597(WNT7A) 102898026(WNT7B)
LAV: 
100660629(WNT7B) 100675463(WNT7A)
MDO: 
100014091(WNT7B)
SHR: 
100925362(WNT7B) 100931119(WNT7A)
OAA: 
100075994(WNT7A)
GGA: 
374168(WNT7A) 427937(WNT7B)
MGP: 
100542203(WNT7B) 100542958(WNT7A)
CJO: 
107317577(WNT7B) 107319707(WNT7A)
APLA: 
101792761(WNT7A) 101805245(WNT7B)
TGU: 
100220226(WNT7B) 100220584(WNT7A)
GFR: 
102043987(WNT7A) 102044794(WNT7B)
FAB: 
101813299(WNT7A) 101816884(WNT7B)
PHI: 
102113507(WNT7B) 102113528(WNT7A)
CCW: 
104695759(WNT7A) 104696093(WNT7B)
FPG: 
101913212(WNT7A) 101919373(WNT7B)
FCH: 
102050340(WNT7B) 102056992(WNT7A)
CLV: 
102084979(WNT7B) 102088082(WNT7A)
AAM: 
106488582(WNT7A) 106488789(WNT7B)
ASN: 
AMJ: 
102568312(WNT7B) 102575772(WNT7A)
PSS: 
102450567(WNT7B) 102452569(WNT7A)
CMY: 
102942821(WNT7B) 102945035(WNT7A)
ACS: 
100553258(wnt7a) 100567981(wnt7b)
PBI: 
GJA: 
107114761(WNT7B) 107118817(WNT7A)
XLA: 
399364(wnt7b.L)
XTR: 
100145124(wnt7b)
DRE: 
100148840(wnt7bb) 563427(wnt7ba) 565714(wnt7aa)
TRU: 
101071438(wnt7b) 101078823(wnt7a)
TNG: 
MZE: 
101464816(wnt7b) 101466313(wnt7a) 101469419(wnt7b) 101484715
OLA: 
XMA: 
SASA: 
LCM: 
CMK: 
103179433(wnt7b) 103185034(wnt7a)
BFO: 
BRAFLDRAFT_56634(AmphiWnt7b)
CIN: 
778938(wnt7)
SPU: 
SKO: 
100313764(Wnt7)
DPO: 
DAN: 
DER: 
DPE: 
DSE: 
DSI: 
Dsimw501_GD10659(Dsim_GD10659)
DWI: 
DYA: 
Dyak_GE19281(dyak_GLEANR_3054)
DGR: 
DMO: 
DVI: 
MDE: 
AGA: 
AAG: 
CQU: 
AME: 
411919(Wnt7)
BIM: 
BTER: 
SOC: 
HST: 
CFO: 
NVI: 
TCA: 
661936(Wnt7)
BMOR: 
DPL: 
PXY: 
API: 
DPX: 
ISC: 
HRO: 
LGI: 
CRG: 
OBI: 
ADF: 
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)
  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)
  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)
  Sequence
[mmu:22421]

DBGET integrated database retrieval system