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Intellectual disability syndromic and non-syndromic v1.562 TMEM251 Zornitza Stark Tag new gene name tag was added to gene: TMEM251.
Intellectual disability syndromic and non-syndromic v1.562 TMEM251 Zornitza Stark Marked gene: TMEM251 as ready
Intellectual disability syndromic and non-syndromic v1.562 TMEM251 Zornitza Stark Gene: tmem251 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v1.562 TMEM251 Zornitza Stark Classified gene: TMEM251 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v1.562 TMEM251 Zornitza Stark Gene: tmem251 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v1.561 TMEM251 Zornitza Stark gene: TMEM251 was added
gene: TMEM251 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: TMEM251 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM251 were set to 40171858; 33252156
Phenotypes for gene: TMEM251 were set to Dysostosis multiplex, Ain-Naz type MIM@619345
Review for gene: TMEM251 was set to GREEN
Added comment: PMID 40171858: reports 2 siblings from an Iranian consanguineous family and six previously reported families (8 patients, 7 unrelated families) with biallelic loss‑of‑function LYSET variants presenting with MLII‑like mucolipidosis; core features include dysostosis multiplex, coarse facial features, hepatomegaly, joint contractures, developmental delay; mouse knockout recapitulates the phenotype, supporting gene‑disease causality.

HGNC approved name is LYSET.
Sources: Literature