Rare syndromic craniosynostosis or isolated multisuture synostosis
Gene: ANKH
Comment on list classification: There are two cases reported in total with craniosynostosis. Hence, this gene can be rated amber.Created: 19 Jul 2023, 7:12 p.m. | Last Modified: 19 Jul 2023, 7:12 p.m.
Panel Version: 4.105
PMID:36118902 reported a single patient with variant in ANKH (c.1129_1132delinsC; p.Phe377del) from a Chinese cohort with syndromic bicoronal and sagittal synostosis. This variant is reported as pathogenic for craniometaphyseal dysplasia in ClinVar and is absent from gnomAD v.2.1.1.
DECIPHER database (https://www.deciphergenomics.org) reported craniosynostosis as one of the clinical presentations in a single patient with heterozygous sequence variant (c.559C>T; p.Arg187Trp) in ANKH gene. This variant was reported as likely pathogenic.
Sources: LiteratureCreated: 19 Jul 2023, 7:11 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Craniometaphyseal dysplasia, OMIM:123000; craniosynostosis, MONDO:0015469
Publications
Gene: ankh has been classified as Amber List (Moderate Evidence).
gene: ANKH was added gene: ANKH was added to Rare syndromic craniosynostosis or isolated multisuture synostosis. Sources: Literature Mode of inheritance for gene: ANKH was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ANKH were set to 36118902; 36980886 Phenotypes for gene: ANKH were set to Craniometaphyseal dysplasia, OMIM:123000; craniosynostosis, MONDO:0015469 Review for gene: ANKH was set to AMBER