KEGG   ORTHOLOGY: K08285Help
Entry
K08285                      KO                                     

Name
TRIM18, MID1
Definition
midline 1 [EC:2.3.2.27]
Pathway
Ubiquitin mediated proteolysis
Disease
H00583  
Opitz-GBBB syndrome
Brite
KEGG Orthology (KO) [BR:ko00001]
 Genetic Information Processing
  Folding, sorting and degradation
   04120 Ubiquitin mediated proteolysis
    K08285  TRIM18, MID1; midline 1
Enzymes [BR:ko01000]
 2. Transferases
  2.3  Acyltransferases
   2.3.2  Aminoacyltransferases
    2.3.2.27  RING-type E3 ubiquitin transferase
     K08285  TRIM18, MID1; midline 1
Ubiquitin system [BR:ko04121]
 Ubiquitin ligases (E3)
  Single Ring-finger type E3
   TRIM/RBCC proteins
    K08285  TRIM18, MID1; midline 1
BRITE hierarchy
Genes
HSA: 
4281(MID1)
PTR: 
741750(MID1)
PPS: 
100970390(MID1)
GGO: 
101147859(MID1)
PON: 
100174199(MID1)
NLE: 
100579343(MID1)
MCC: 
709683(MID1)
MCF: 
102130085(MID1)
RRO: 
CJC: 
100389533(MID1)
MMU: 
17318(Mid1)
RNO: 
54252(Mid1)
CGE: 
100758489(Mid1)
NGI: 
103749977(Mid1)
HGL: 
101701977(Mid1)
OCU: 
TUP: 
102491156(MID1)
CFA: 
491737(MID1)
AML: 
100468400(MID1)
UMR: 
103668093(MID1)
FCA: 
101085021(MID1)
PTG: 
102966170(MID1)
BTA: 
534604(MID1)
BOM: 
102268511(MID1)
PHD: 
102328059(MID1)
CHX: 
102174822(MID1)
OAS: 
101117818(MID1)
SSC: 
100524415(MID1)
CFR: 
102518817(MID1)
BACU: 
103013073(MID1)
LVE: 
103085610(MID1)
ECB: 
100049999(MID1)
MYB: 
102240796(MID1)
MYD: 
102773634(MID1)
PALE: 
102897002(MID1)
MDO: 
100018227(MID1)
SHR: 
100925173(MID1)
OAA: 
100082209(MID1)
GGA: 
373920(MID1)
MGP: 
100544167(MID1)
CJO: 
107325797(MID1)
APLA: 
101796423(MID1)
TGU: 
100230380(MID1)
GFR: 
102040330(MID1)
FAB: 
101821567(MID1)
PHI: 
102103044(MID1)
CCW: 
104686143(MID1)
FPG: 
101922750(MID1)
FCH: 
102053970(MID1)
CLV: 
102083555(MID1)
AAM: 
106491602(MID1)
ASN: 
102374310(MID1)
AMJ: 
102576737(MID1)
PSS: 
102449757(MID1)
CMY: 
102935002(MID1)
ACS: 
100556113(mid1)
PBI: 
103051810(MID1)
GJA: 
107120436(MID1)
XLA: 
100463496(mid1)
XTR: 
448651(mid1)
DRE: 
100330952(mid1)
TRU: 
MZE: 
OLA: 
XMA: 
LCM: 
102351326(MID1)
CMK: 
103177517(mid1)
BFO: 
CIN: 
SKO: 
CRG: 
105346521(Midline-1)
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Trockenbacher A, Suckow V, Foerster J, Winter J, Krauss S, Ropers HH, Schneider R, Schweiger S
  Title
MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation.
  Journal
Nat Genet 29:287-94 (2001)
  Sequence
[hsa:4281]

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