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Mendeliome v1.2818 OGFRL1 Zornitza Stark Marked gene: OGFRL1 as ready
Mendeliome v1.2818 OGFRL1 Zornitza Stark Gene: ogfrl1 has been classified as Red List (Low Evidence).
Mendeliome v1.2818 OGFRL1 Zornitza Stark Classified gene: OGFRL1 as Red List (low evidence)
Mendeliome v1.2818 OGFRL1 Zornitza Stark Gene: ogfrl1 has been classified as Red List (Low Evidence).
Mendeliome v1.2817 OGFRL1 Rylee Peters gene: OGFRL1 was added
gene: OGFRL1 was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: OGFRL1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: OGFRL1 were set to PMID: 38699440
Phenotypes for gene: OGFRL1 were set to Cherubism (MONDO:0007315), OGFRL1-related
Review for gene: OGFRL1 was set to RED
Added comment: 3x individuals from 2 unrelated families with cherubism and homozygous NMD-predicted variants in OGFRL1.

In one family, the NMD-predicted OGFRL1 variant was identified in 2x affected individuals and was either heterozygous or absent in 7x unaffected family members tested.

OGFRL1 knockout mice and mice carrying a patient frameshift mutation were generated, however, neither mouse model recapitulated human cherubism.

Absence of homozygous LoF variants in gnomAD v4.
Sources: Literature