Callosome
Gene: NONOEnsemblGeneIds (GRCh38): ENSG00000147140
EnsemblGeneIds (GRCh37): ENSG00000147140
OMIM: 300084, Gene2Phenotype
NONO is in 6 panels
1 review
Krithika Murali (Victorian Clinical Genetics Services)
Syndromic ID with associated features reported including corpus callosum and cardiac anomalies.
Sources: LiteratureCreated: 23 Mar 2022, 10:23 p.m.
Mode of inheritance
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967
Publications
Details
- Mode of Inheritance
- X-LINKED: hemizygous mutation in males, biallelic mutations in females
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967
- OMIM
- 300084
- Clinvar variants
- Variants in NONO
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: nono has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: nono has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Krithika Murali (Victorian Clinical Genetics Services)gene: NONO was added gene: NONO was added to Callosome. Sources: Literature Mode of inheritance for gene: NONO was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Publications for gene: NONO were set to 26571461; 27329731; 27550220 Phenotypes for gene: NONO were set to Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967 Review for gene: NONO was set to GREEN