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Date	Panel	Item	Activity
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15 Jan 2021	Rare multisystem ciliopathy disorders v1.136	KIF14	Arina Puzriakova Phenotypes for gene: KIF14 were changed from intrauterine growth restriction (IUGR); microcephaly; renal cystic dysplasia/agenesis; complex brain malformation; genitourinary malformation; ?Meckel syndrome 12, 616258; Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome; ?Meckel syndrome 12 to Meckel syndrome 12, OMIM:616258; Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome, MONDO:0014552
25 Jan 2017	Rare multisystem ciliopathy disorders	KIF14	Alice Gardham marked KIF14 as ready
25 Jan 2017	Rare multisystem ciliopathy disorders	KIF14	Alice Gardham commented on KIF14