|
| Entrez Id: |
341640 |
| Gene Symbol: |
FREM2 |
FREM2
|
0.400 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
|
24700879 |
2014 |
|
| Entrez Id: |
341640 |
| Gene Symbol: |
FREM2 |
FREM2
|
0.400 |
GermlineCausalMutation
|
disease |
ORPHANET |
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis.
|
21900877 |
2012 |
|
| Entrez Id: |
80000 |
| Gene Symbol: |
GREB1L |
GREB1L
|
0.310 |
GermlineCausalMutation
|
disease |
ORPHANET |
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
|
29100090 |
2017 |
|
| Entrez Id: |
80000 |
| Gene Symbol: |
GREB1L |
GREB1L
|
0.310 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
|
29100091 |
2017 |
|
| Entrez Id: |
80144 |
| Gene Symbol: |
FRAS1 |
FRAS1
|
0.310 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
|
24700879 |
2014 |
|
| Entrez Id: |
5979 |
| Gene Symbol: |
RET |
RET
|
0.310 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.
|
24429398 |
2014 |
|
| Entrez Id: |
5979 |
| Gene Symbol: |
RET |
RET
|
0.310 |
GermlineCausalMutation
|
disease |
ORPHANET |
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis.
|
21900877 |
2012 |
|
| Entrez Id: |
80144 |
| Gene Symbol: |
FRAS1 |
FRAS1
|
0.310 |
GermlineCausalMutation
|
disease |
ORPHANET |
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis.
|
21900877 |
2012 |
|
| Entrez Id: |
158326 |
| Gene Symbol: |
FREM1 |
FREM1
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Clinical implications of the solitary functioning kidney.
|
24370773 |
2014 |
|
| Entrez Id: |
25778 |
| Gene Symbol: |
DSTYK |
DSTYK
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutations in DSTYK and dominant urinary tract malformations.
|
23862974 |
2013 |
|
| Entrez Id: |
652 |
| Gene Symbol: |
BMP4 |
BMP4
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis.
|
21900877 |
2012 |
|
| Entrez Id: |
158326 |
| Gene Symbol: |
FREM1 |
FREM1
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Congenital anomalies of kidney and urinary tract.
|
20807610 |
2010 |
|
| Entrez Id: |
25778 |
| Gene Symbol: |
DSTYK |
DSTYK
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33.
|
17273976 |
2007 |
|
| Entrez Id: |
7380 |
| Gene Symbol: |
UPK3A |
UPK3A
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.
|
15888565 |
2005 |