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Ataxia and cerebellar anomalies - narrow panel v8.23 CDK5 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to promote this gene to Green at the next GMS panel update - 2 unrelated families with the same severe phenotype comprising lissencephaly with cerebellar hypoplasia and supportive animal models. Other lissencephaly genes also included on this panel (RELN, TUBA1A)
Ataxia and cerebellar anomalies - narrow panel v0.5 RELN Ellen McDonagh gene: RELN was added
gene: RELN was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green
Mode of inheritance for gene: RELN was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RELN were set to 10973257
Phenotypes for gene: RELN were set to Lissencephaly 2, 257320