KEGG   ORTHOLOGY: K05729Help
Entry
K05729                      KO                                     

Name
ARHGEF6, PIXA
Definition
Rho guanine nucleotide exchange factor 6
Pathway
Regulation of actin cytoskeleton
Pancreatic cancer
Disease
H00480  
Non-syndromic X-linked mental retardation
Brite
KEGG Orthology (KO) [BR:ko00001]
 Cellular Processes
  Cell motility
   04810 Regulation of actin cytoskeleton
    K05729  ARHGEF6, PIXA; Rho guanine nucleotide exchange factor 6
 Human Diseases
  Cancers
   05212 Pancreatic cancer
    K05729  ARHGEF6, PIXA; Rho guanine nucleotide exchange factor 6
BRITE hierarchy
Other DBs
GO: 
Genes
HSA: 
9459(ARHGEF6)
PTR: 
473803(ARHGEF6)
PPS: 
100974851(ARHGEF6)
GGO: 
101152069(ARHGEF6)
PON: 
100434767(ARHGEF6)
MCC: 
693976(ARHGEF6)
MCF: 
102138998(ARHGEF6)
MMU: 
73341(Arhgef6)
RNO: 
363509(Arhgef6)
CGE: 
100762795(Arhgef6)
HGL: 
101700245(Arhgef6)
TUP: 
102488196(ARHGEF6)
CFA: 
610290(ARHGEF6)
AML: 
100467664(ARHGEF6)
FCA: 
101099030(ARHGEF6)
PTG: 
102969652(ARHGEF6)
BTA: 
533823(ARHGEF6)
BOM: 
102269505(ARHGEF6)
PHD: 
102320069(ARHGEF6)
CHX: 
102172607(ARHGEF6)
SSC: 
100622228(ARHGEF6)
CFR: 
BACU: 
103012611(ARHGEF6)
LVE: 
103069913(ARHGEF6)
ECB: 
100056622(ARHGEF6)
MYB: 
102256281(ARHGEF6)
MYD: 
102762553(ARHGEF6)
PALE: 
102885217(ARHGEF6)
MDO: 
100010264(ARHGEF6)
SHR: 
100919550(ARHGEF6)
OAA: 
100083576(ARHGEF6)
GGA: 
422247(ARHGEF6)
MGP: 
TGU: 
100228811(ARHGEF6)
FAB: 
101808339(ARHGEF6)
PHI: 
102107901(ARHGEF6)
APLA: 
101805138(ARHGEF6)
FPG: 
101910918(ARHGEF6)
FCH: 
102059226(ARHGEF6)
CLV: 
102086829(ARHGEF6)
ASN: 
102379973(ARHGEF6)
AMJ: 
102574657(ARHGEF6)
PSS: 
102461283(ARHGEF6)
CMY: 
102945357(ARHGEF6)
ACS: 
PBI: 
103061511(ARHGEF6)
XTR: 
100489192(arhgef6)
DRE: 
TRU: 
MZE: 
OLA: 
XMA: 
LCM: 
102348209(ARHGEF6)
CMK: 
103178151(arhgef6)
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Lower KM, Gecz J
  Title
Characterization of ARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for X-linked mental retardation: mutation screening in Borjeson-Forssman-Lehmann syndrome and MRX27.
  Journal
Am J Med Genet 100:43-8 (2001)
  Sequence
[hsa:9459]

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