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Intellectual disability syndromic and non-syndromic v0.4861 TMEM63C Zornitza Stark Phenotypes for gene: TMEM63C were changed from Hereditary spastic paraplegia, MONDO:0019064, TMEM63C-related to Spastic paraplegia 87, autosomal recessive, MIM# 619966
Intellectual disability syndromic and non-syndromic v0.4860 TMEM63C Zornitza Stark reviewed gene: TMEM63C: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 87, autosomal recessive, MIM# 619966; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.4843 TMEM63C Elena Savva Classified gene: TMEM63C as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.4843 TMEM63C Elena Savva Gene: tmem63c has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.4842 TMEM63C Elena Savva Classified gene: TMEM63C as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.4842 TMEM63C Elena Savva Gene: tmem63c has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.4842 TMEM63C Elena Savva Classified gene: TMEM63C as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.4842 TMEM63C Elena Savva Gene: tmem63c has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.4841 TMEM63C Elena Savva Marked gene: TMEM63C as ready
Intellectual disability syndromic and non-syndromic v0.4841 TMEM63C Elena Savva Gene: tmem63c has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.4841 TMEM63C Elena Savva gene: TMEM63C was added
gene: TMEM63C was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: TMEM63C was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM63C were set to PMID: 35718349
Phenotypes for gene: TMEM63C were set to Hereditary spastic paraplegia, MONDO:0019064, TMEM63C-related
Review for gene: TMEM63C was set to GREEN
Added comment: PMID: 35718349 - Four NMD PTCs observed in at least 3 unrelated patients. Two segregated strongly in highly consanguineous families.
Common clinical details include mild ID, spastic paraplegia, hypereflexia, spasticity, delayed motor development.
Sources: Literature