Growth failure in early childhood
Gene: NLRP7EnsemblGeneIds (GRCh38): ENSG00000167634
EnsemblGeneIds (GRCh37): ENSG00000167634
OMIM: 609661, Gene2Phenotype
NLRP7 is in 2 panels
3 reviews
Ivone Leong (Genomics England Curator)
Submitted on behalf of NHS GMS "This gene does not go on the panel as linked to MLID and suggest separate panel for this. Genes NLRP5, NLRP7, PAD16, NLRP2 & KHDC3L"Created: 3 Mar 2022, 1:49 p.m. | Last Modified: 3 Mar 2022, 1:49 p.m.
Panel Version: 1.100
After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed.Created: 3 Mar 2022, 1:49 p.m. | Last Modified: 3 Mar 2022, 1:49 p.m.
Panel Version: 1.100
Sarah Leigh (Genomics England Curator)
Comment on mode of inheritance: Review from Eamonn Maher: I think it would be better that these are maternal effect genes for which biallelic variants in a healthy women cause a reproductive phenotype that may include miscarriage, hydatidiform mole or children with a congenital imprinting disorderCreated: 21 Apr 2021, 2:43 p.m. | Last Modified: 21 Apr 2021, 2:43 p.m.
Panel Version: 1.61
Comment on mode of inheritance: MOI based on review from Professor Karen Temple (Clinical Genetics, University Hospital Southampton NHS Foundation Trust).Created: 2 Feb 2021, 2:36 p.m. | Last Modified: 2 Feb 2021, 2:36 p.m.
Panel Version: 1.50
Comment on list classification: Based on review from Professor Karen Temple (Clinical Genetics, University Hospital Southampton NHS Foundation Trust) for the involvement of NLRP7 variants in Multi Locus Imprinting DisturbanceCreated: 1 Feb 2021, 8:53 a.m. | Last Modified: 2 Feb 2021, 2:47 p.m.
Panel Version: 1.52
Karen Temple (Wessex GMC)
NOte that this gene is tested for in recurrent hydatidiform mole. But some pregnancies progress with growth disorders due to multilocus imprinting disturbance. This can missed on genome testing and so patients require methylation testing at imprinted loci to confirm The mutation in NLRP7 is in the mother of the proband.
Sources: Expert listCreated: 29 Jan 2021, 11:11 a.m.
Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
IUGR; Short stature; fetal wastage
Publications
- Eur J Hum Genet. 2017 Aug
- 25(8):924-929. PMID: 28561018 doi: 10.1038/ejhg.2017.94. Epub 2017 May 31. Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring. Soellner L(1), Begemann M(1), Degenhardt F(2), Geipel A(3), Eggermann T(1), Mangold E(2).
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Phenotypes
-
- IUGR
- Short stature
- fetal wastage
- Multi Locus Imprinting Disturbance
- Hydatidiform mole, recurrent, 1 OMIM:231090
- hydatidiform mole, recurrent, 1 MONDO:0009273
- OMIM
- 609661
- Clinvar variants
- Variants in NLRP7
- Penetrance
- unknown
- Publications
- Panels with this gene
History Filter Activity
Removed Tag
Ivone Leong (Genomics England Curator)Tag for-review was removed from gene: NLRP7.
Set mode of inheritance
Sarah Leigh (Genomics England Curator)Mode of inheritance for gene: NLRP7 was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for gene: NLRP7 were changed from IUGR; Short stature; fetal wastage; Multi Locus Imprinting Disturbance to IUGR; Short stature; fetal wastage; Multi Locus Imprinting Disturbance; Hydatidiform mole, recurrent, 1 OMIM:231090; hydatidiform mole, recurrent, 1 MONDO:0009273
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for gene: NLRP7 were changed from IUGR; Short stature; fetal wastage to IUGR; Short stature; fetal wastage; Multi Locus Imprinting Disturbance
Set mode of inheritance
Sarah Leigh (Genomics England Curator)Mode of inheritance for gene: NLRP7 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Entity classified by Genomics England curator
Sarah Leigh (Genomics England Curator)Gene: nlrp7 has been classified as Amber List (Moderate Evidence).
Set publications
Sarah Leigh (Genomics England Curator)Publications for gene: NLRP7 were set to Eur J Hum Genet. 2017 Aug; 25(8):924-929. PMID: 28561018 doi: 10.1038/ejhg.2017.94. Epub 2017 May 31. Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring. Soellner L(1), Begemann M(1), Degenhardt F(2), Geipel A(3), Eggermann T(1), Mangold E(2).
Added Tag
Sarah Leigh (Genomics England Curator)Tag for-review tag was added to gene: NLRP7.
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes, Set penetrance
Karen Temple (Wessex GMC)gene: NLRP7 was added gene: NLRP7 was added to Growth failure in early childhood. Sources: Expert list Mode of inheritance for gene: NLRP7 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: NLRP7 were set to Eur J Hum Genet. 2017 Aug; 25(8):924-929. PMID: 28561018 doi: 10.1038/ejhg.2017.94. Epub 2017 May 31. Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring. Soellner L(1), Begemann M(1), Degenhardt F(2), Geipel A(3), Eggermann T(1), Mangold E(2). Phenotypes for gene: NLRP7 were set to IUGR; Short stature; fetal wastage Penetrance for gene: NLRP7 were set to unknown Review for gene: NLRP7 was set to GREEN