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| Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.21 | CBWD1 | Zornitza Stark Marked gene: CBWD1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.21 | CBWD1 | Zornitza Stark Gene: cbwd1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.21 | CBWD1 |
Zornitza Stark gene: CBWD1 was added gene: CBWD1 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic_VCGS. Sources: Literature Mode of inheritance for gene: CBWD1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CBWD1 were set to 31862704 Phenotypes for gene: CBWD1 were set to CAKUT Review for gene: CBWD1 was set to RED Added comment: A pair of siblings with homozygous deletion in this gene reported; functional data including animal model. Sources: Literature |
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