|
SLC39A13
|
0.300 |
Biomarker
|
group |
CTD_human |
Zinc balance is critical for NFI-C mediated regulation of odontoblast differentiation.
|
22228435 |
2012 |
|
| Entrez Id: |
54499 |
| Gene Symbol: |
TMCO1 |
TMCO1
|
0.300 |
Biomarker
|
group |
CTD_human |
Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation.
|
20018682 |
2010 |
|
SLC39A13
|
0.300 |
Biomarker
|
group |
CTD_human |
The zinc transporter SLC39A13/ZIP13 is required for connective tissue development; its involvement in BMP/TGF-beta signaling pathways.
|
18985159 |
2008 |
|
| Entrez Id: |
56172 |
| Gene Symbol: |
ANKH |
ANKH
|
0.300 |
Biomarker
|
group |
CTD_human |
Dental anomalies in a child with craniometaphysial dysplasia.
|
18027777 |
2007 |
|
| Entrez Id: |
4038 |
| Gene Symbol: |
LRP4 |
LRP4
|
0.300 |
Biomarker
|
group |
CTD_human |
Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice.
|
16207730 |
2005 |
|
| Entrez Id: |
860 |
| Gene Symbol: |
RUNX2 |
RUNX2
|
0.300 |
Biomarker
|
group |
CTD_human |
Phenotypic changes in dentition of Runx2 homozygote-null mutant mice.
|
14688224 |
2004 |
|
| Entrez Id: |
4487 |
| Gene Symbol: |
MSX1 |
MSX1
|
0.300 |
Biomarker
|
group |
CTD_human |
MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia.
|
14630905 |
2003 |
|
| Entrez Id: |
2263 |
| Gene Symbol: |
FGFR2 |
FGFR2
|
0.300 |
Biomarker
|
group |
CTD_human |
An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.
|
10631169 |
2000 |
|
| Entrez Id: |
5308 |
| Gene Symbol: |
PITX2 |
PITX2
|
0.300 |
Biomarker
|
group |
CTD_human |
Function of Rieger syndrome gene in left-right asymmetry and craniofacial development.
|
10499585 |
1999 |
|
| Entrez Id: |
6926 |
| Gene Symbol: |
TBX3 |
TBX3
|
0.300 |
Biomarker
|
group |
CTD_human |
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome.
|
9207801 |
1997 |
|
| Entrez Id: |
5080 |
| Gene Symbol: |
PAX6 |
PAX6
|
0.300 |
Biomarker
|
group |
CTD_human |
Genetic background effects on dental and other craniofacial abnormalities in homozygous small eye (Pax6Sey/Pax6Sey) mice.
|
9363853 |
1997 |
|
| Entrez Id: |
5080 |
| Gene Symbol: |
PAX6 |
PAX6
|
0.300 |
Biomarker
|
group |
CTD_human |
Craniofacial abnormalities in homozygous Small eye (Sey/Sey) embryos and newborn mice.
|
7559133 |
1995 |
|
| Entrez Id: |
80326 |
| Gene Symbol: |
WNT10A |
WNT10A
|
0.110 |
GeneticVariation
|
group |
BEFREE |
Human WNT10A mutations are associated with developmental tooth abnormalities and adolescent onset of a broad range of ectodermal defects.
|
28589954 |
2017 |
|
| Entrez Id: |
80326 |
| Gene Symbol: |
WNT10A |
WNT10A
|
0.110 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
9533 |
| Gene Symbol: |
POLR1C |
POLR1C
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
5818 |
| Gene Symbol: |
NECTIN1 |
NECTIN1
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
54880 |
| Gene Symbol: |
BCOR |
BCOR
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
126695 |
| Gene Symbol: |
KDF1 |
KDF1
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
64840 |
| Gene Symbol: |
PORCN |
PORCN
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
1717 |
| Gene Symbol: |
DHCR7 |
DHCR7
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
9361 |
| Gene Symbol: |
LONP1 |
LONP1
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
PPP1R13L
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
6949 |
| Gene Symbol: |
TCOF1 |
TCOF1
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
10743 |
| Gene Symbol: |
RAI1 |
RAI1
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
|
| Entrez Id: |
2316 |
| Gene Symbol: |
FLNA |
FLNA
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|