Activity
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3 actions
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| Fetal anomalies v8.26 | NRIP1 | Ida Ertmanska commented on gene: NRIP1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | NRIP1 | Tessa Homfray reviewed gene: NRIP1: Rating: AMBER; Mode of pathogenicity: ; Publications: 41868040, 34525250, 28381549; Phenotypes: Congenital anomalies of kidney and urinary tract 3, OMIM:618270, congenital anomalies of kidney and urinary tract 3, MONDO:0032646; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | NRIP1 |
Ida Ertmanska gene: NRIP1 was added gene: NRIP1 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: NRIP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: NRIP1 were set to 41868040; 34525250; 28381549 Phenotypes for gene: NRIP1 were set to Congenital anomalies of kidney and urinary tract 3, OMIM:618270; congenital anomalies of kidney and urinary tract 3, MONDO:0032646 |
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