Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
GeneticVariation
|
disease |
BEFREE |
A mutation in the B-box region of TRIM32 has also been shown to result in a more pleiotropic disorder, Bardet-Biedl Syndrome (BBS11).
|
21496629 |
2011 |
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
Biomarker
|
disease |
BEFREE |
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
|
16606853 |
2006 |
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
|
16606853 |
2006 |
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
GeneticVariation
|
disease |
UNIPROT |
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
|
16606853 |
2006 |
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene.
|
11822024 |
2002 |
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Entrez Id: |
22954 |
Gene Symbol: |
TRIM32 |
TRIM32
|
0.720 |
Biomarker
|
disease |
CTD_human |
|
|
|
Entrez Id: |
23245 |
Gene Symbol: |
ASTN2 |
ASTN2
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Entrez Id: |
23245 |
Gene Symbol: |
ASTN2 |
ASTN2
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Entrez Id: |
79594 |
Gene Symbol: |
MUL1 |
MUL1
|
0.010 |
Biomarker
|
disease |
BEFREE |
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
|
16606853 |
2006 |
Entrez Id: |
5071 |
Gene Symbol: |
PRKN |
PRKN
|
0.010 |
Biomarker
|
disease |
BEFREE |
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
|
16606853 |
2006 |
Entrez Id: |
158506 |
Gene Symbol: |
CBLL2 |
CBLL2
|
0.010 |
Biomarker
|
disease |
BEFREE |
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
|
16606853 |
2006 |