Entrez Id: |
8626 |
Gene Symbol: |
TP63 |
TP63
|
0.720 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
652 |
Gene Symbol: |
BMP4 |
BMP4
|
0.430 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
23133 |
Gene Symbol: |
PHF8 |
PHF8
|
0.420 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
57822 |
Gene Symbol: |
GRHL3 |
GRHL3
|
0.400 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
7021 |
Gene Symbol: |
TFAP2B |
TFAP2B
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
340419 |
Gene Symbol: |
RSPO2 |
RSPO2
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
4487 |
Gene Symbol: |
MSX1 |
MSX1
|
0.700 |
SusceptibilityMutation
|
disease |
ORPHANET |
MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate.
|
12807959 |
2003 |
Entrez Id: |
80204 |
Gene Symbol: |
FBXO11 |
FBXO11
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.
|
17035249 |
2006 |
Entrez Id: |
8626 |
Gene Symbol: |
TP63 |
TP63
|
0.720 |
SusceptibilityMutation
|
disease |
ORPHANET |
A mutation of the p63 gene in non-syndromic cleft lip.
|
16740912 |
2006 |
Entrez Id: |
3664 |
Gene Symbol: |
IRF6 |
IRF6
|
0.900 |
Biomarker
|
disease |
CTD_human |
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6).
|
17041601 |
2006 |
Entrez Id: |
5727 |
Gene Symbol: |
PTCH1 |
PTCH1
|
0.420 |
Biomarker
|
disease |
CTD_human |
Contributions of PTCH gene variants to isolated cleft lip and palate.
|
16405370 |
2006 |
Entrez Id: |
3664 |
Gene Symbol: |
IRF6 |
IRF6
|
0.900 |
Biomarker
|
disease |
CTD_human |
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip.
|
18836445 |
2008 |
Entrez Id: |
7020 |
Gene Symbol: |
TFAP2A |
TFAP2A
|
0.410 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome.
|
10767004 |
2000 |
Entrez Id: |
6573 |
Gene Symbol: |
SLC19A1 |
SLC19A1
|
0.310 |
Biomarker
|
disease |
CTD_human |
Folate pathway and nonsyndromic cleft lip and palate.
|
21254359 |
2011 |
Entrez Id: |
7298 |
Gene Symbol: |
TYMS |
TYMS
|
0.310 |
Biomarker
|
disease |
CTD_human |
Folate pathway and nonsyndromic cleft lip and palate.
|
21254359 |
2011 |
Entrez Id: |
4548 |
Gene Symbol: |
MTR |
MTR
|
0.310 |
Biomarker
|
disease |
CTD_human |
Folate pathway and nonsyndromic cleft lip and palate.
|
21254359 |
2011 |
Entrez Id: |
10588 |
Gene Symbol: |
MTHFS |
MTHFS
|
0.300 |
Biomarker
|
disease |
CTD_human |
Folate pathway and nonsyndromic cleft lip and palate.
|
21254359 |
2011 |
Entrez Id: |
23743 |
Gene Symbol: |
BHMT2 |
BHMT2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Folate pathway and nonsyndromic cleft lip and palate.
|
21254359 |
2011 |
Entrez Id: |
4846 |
Gene Symbol: |
NOS3 |
NOS3
|
0.300 |
Biomarker
|
disease |
CTD_human |
Folate pathway and nonsyndromic cleft lip and palate.
|
21254359 |
2011 |
Entrez Id: |
8626 |
Gene Symbol: |
TP63 |
TP63
|
0.720 |
Biomarker
|
disease |
CTD_human |
Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.
|
16688749 |
2006 |
Entrez Id: |
4609 |
Gene Symbol: |
MYC |
MYC
|
0.300 |
Biomarker
|
disease |
CTD_human |
Long-range enhancers regulating Myc expression are required for normal facial morphogenesis.
|
24859337 |
2014 |
Entrez Id: |
8626 |
Gene Symbol: |
TP63 |
TP63
|
0.720 |
SusceptibilityMutation
|
disease |
ORPHANET |
Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate.
|
21567929 |
2011 |
Entrez Id: |
144100 |
Gene Symbol: |
PLEKHA7 |
PLEKHA7
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
|
29805042 |
2018 |
Entrez Id: |
80004 |
Gene Symbol: |
ESRP2 |
ESRP2
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
|
29805042 |
2018 |
Entrez Id: |
54477 |
Gene Symbol: |
PLEKHA5 |
PLEKHA5
|
0.300 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
|
29805042 |
2018 |