Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Exome sequencing on malignant meningiomas identified mutations in neurofibromatosis type 2 (NF2) and meningioma 1 (MN1) genes.
|
25549701 |
2014 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Recessive and dominant mutations in retinoic acid receptor beta in cases with microphthalmia and diaphragmatic hernia.
|
24075189 |
2013 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature.
|
22436304 |
2012 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Meningioma 1 is required for appropriate osteoblast proliferation, motility, differentiation, and function.
|
19386590 |
2009 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources.
|
19919682 |
2009 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
|
19344873 |
2009 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice.
|
18948418 |
2008 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
The 1,25(OH)2D3-regulated transcription factor MN1 stimulates vitamin D receptor-mediated transcription and inhibits osteoblastic cell proliferation.
|
15890672 |
2005 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Targeted disruption of the Mn1 oncogene results in severe defects in development of membranous bones of the cranial skeleton.
|
15870292 |
2005 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
The MN1 oncoprotein synergizes with coactivators RAC3 and p300 in RAR-RXR-mediated transcription.
|
12569362 |
2003 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
|
11559848 |
2001 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
The MN1-TEL fusion protein, encoded by the translocation (12;22)(p13;q11) in myeloid leukemia, is a transcription factor with transforming activity.
|
11094079 |
2000 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma.
|
7731706 |
1995 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11.
|
7731705 |
1995 |