×
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:
7055
Gene Symbol:
THAS
THAS
0.300
Biomarker
disease
CTD_human
X-linked midline defects.
4039891
1985
×
Entrez Id:
5818
Gene Symbol:
NECTIN1
NECTIN1
0.640
Biomarker
disease
GENOMICS_ENGLAND
Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia.
10932188
2000
×
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:
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:
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:
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:
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:
5818
Gene Symbol:
NECTIN1
NECTIN1
0.640
SusceptibilityMutation
disease
ORPHANET
Study of the PVRL1 gene in Italian nonsyndromic cleft lip patients with or without cleft palate.
16674562
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:
4524
Gene Symbol:
MTHFR
MTHFR
0.390
Biomarker
disease
CTD_human
Variable contribution of the MTHFR C677T polymorphism to non-syndromic cleft lip and palate risk in China.
16470725
2006
×
Entrez Id:
7341
Gene Symbol:
SUMO1
SUMO1
0.320
Biomarker
disease
CTD_human
SUMO1 haploinsufficiency leads to cleft lip and palate.
16990542
2006
×
Entrez Id:
6948
Gene Symbol:
TCN2
TCN2
0.310
Biomarker
disease
CTD_human
Study of four genes belonging to the folate pathway: transcobalamin 2 is involved in the onset of non-syndromic cleft lip with or without cleft palate.
16470748
2006
×
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:
3664
Gene Symbol:
IRF6
IRF6
0.900
SusceptibilityMutation
disease
ORPHANET
This study aimed to confirm the contribution of IRF6 to cleft lip with or without palate risk in additional Asian populations.
17438386
2007
×
Entrez Id:
2260
Gene Symbol:
FGFR1
FGFR1
0.430
Biomarker
disease
CTD_human
Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases.
17963255
2007
×
Entrez Id:
2253
Gene Symbol:
FGF8
FGF8
0.400
Biomarker
disease
CTD_human
Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases.
17963255
2007
×
Entrez Id:
2255
Gene Symbol:
FGF10
FGF10
0.310
Biomarker
disease
CTD_human
Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases.
17963255
2007
×
Entrez Id:
2252
Gene Symbol:
FGF7
FGF7
0.310
Biomarker
disease
CTD_human
Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases.
17963255
2007
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.310
Biomarker
disease
CTD_human
Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases.
17963255
2007