Microphthalmia, Syndromic 5
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
Retinal Dystrophies
|
0.410 |
Biomarker
|
group |
GENOMICS_ENGLAND |
|
|
|
Panhypopituitarism
|
0.350 |
Biomarker
|
disease |
CTD_human |
|
|
|
Disorder of eye
|
0.320 |
Biomarker
|
group |
GENOMICS_ENGLAND |
|
|
|
Disorder of eye
|
0.320 |
Biomarker
|
group |
GENOMICS_ENGLAND |
|
|
|
Microphthalmia, Syndromic 5
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
The human homeodomain protein OTX2 binds to the human tenascin-C promoter and trans-represses its activity in transfected cells.
|
9174161 |
1997 |
Congenital small ears
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
The human homeodomain protein OTX2 binds to the human tenascin-C promoter and trans-represses its activity in transfected cells.
|
9174161 |
1997 |
Jaw Abnormalities
|
0.300 |
Biomarker
|
group |
CTD_human |
Genetic modifiers of otocephalic phenotypes in Otx2 heterozygous mutant mice.
|
12183386 |
2002 |
Microphthalmia, Syndromic 5
|
0.700 |
GermlineCausalMutation
|
disease |
ORPHANET |
Heterozygous mutations of OTX2 cause severe ocular malformations.
|
15846561 |
2005 |
Microphthalmia, Syndromic 5
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Heterozygous mutations of OTX2 cause severe ocular malformations.
|
15846561 |
2005 |
Microphthalmia, Syndromic 5
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Heterozygous mutations of OTX2 cause severe ocular malformations.
|
15846561 |
2005 |
Bipolar Disorder
|
0.310 |
Biomarker
|
disease |
PSYGENET |
Based on this positive case-control association finding, we conclude that variations in OTX2 might confer risk for the development of bipolar disorder.
|
17541950 |
2007 |
Microphthalmia, Syndromic 5
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
OTX2 mutation in a patient with anophthalmia, short stature, and partial growth hormone deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters.
|
18628516 |
2008 |
PITUITARY HORMONE DEFICIENCY, COMBINED, 6
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.
|
18728160 |
2008 |
Pituitary Hormone Deficiency, Combined, 1
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.
|
18728160 |
2008 |
Microphthalmia, Syndromic 5
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma.
|
18781617 |
2008 |
Medulloblastoma
|
0.400 |
Biomarker
|
disease |
CTD_human |
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
|
19270706 |
2009 |
Childhood Medulloblastoma
|
0.400 |
Biomarker
|
disease |
CTD_human |
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
|
19270706 |
2009 |
Adult Medulloblastoma
|
0.400 |
Biomarker
|
disease |
CTD_human |
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
|
19270706 |
2009 |
Medullomyoblastoma
|
0.310 |
Biomarker
|
disease |
CTD_human |
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
|
19270706 |
2009 |
Desmoplastic Medulloblastoma
|
0.300 |
Biomarker
|
disease |
CTD_human |
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
|
19270706 |
2009 |
Melanotic medulloblastoma
|
0.300 |
Biomarker
|
disease |
CTD_human |
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
|
19270706 |
2009 |
Microphthalmia, Syndromic 5
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction.
|
19956411 |
2009 |
Microphthalmia, Syndromic 5
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype.
|
19965921 |
2010 |
PITUITARY HORMONE DEFICIENCY, COMBINED, 6
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype.
|
19965921 |
2010 |