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| Multi locus imprinting disorders v1.15 | NLRP2 | Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #620332) and the OMIM record was last accessed on 18 December 2025. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Multi locus imprinting disorders v1.15 | NLRP2 | Achchuthan Shanmugasundram Phenotypes for gene: NLRP2 were changed from Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 MONDO:0016475 to Oocyte/zygote/embryo maturation arrest 18, OMIM:620332; oocyte/zygote/embryo maturation arrest 18, MONDO:0957230; Beckwith-Wiedemann syndrome due to imprinting defect of 11p15, MONDO:0016475 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Multi locus imprinting disorders v1.14 | NLRP2 | Achchuthan Shanmugasundram Tag watchlist tag was added to gene: NLRP2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Multi locus imprinting disorders v1.14 | NLRP2 |
Achchuthan Shanmugasundram Tag watchlist was removed from gene: NLRP2. Tag gene-checked was removed from gene: NLRP2. |
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| Multi locus imprinting disorders v0.14 | NLRP2 | Arina Puzriakova Tag gene-checked tag was added to gene: NLRP2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Multi locus imprinting disorders v0.6 | NLRP2 | Sarah Leigh Entity copied from Genomic imprinting v0.137 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Multi locus imprinting disorders v0.6 | NLRP2 |
Sarah Leigh gene: NLRP2 was added gene: NLRP2 was added to Multi locus imprinting disorders. Sources: Imprinting GeCIP Subdomain,Expert Review Green watchlist tags were added to gene: NLRP2. Mode of inheritance for gene: NLRP2 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal Publications for gene: NLRP2 were set to 19300480; 30221575; 32169557; 28422141; 28317850; 26323243; 29574422; 30877238; 33090377 Phenotypes for gene: NLRP2 were set to Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 MONDO:0016475 Penetrance for gene: NLRP2 were set to Complete Mode of pathogenicity for gene: NLRP2 was set to Other |
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