- May 2022
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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DICER1 syndrome is a rare genetic condition predisposing to hereditary cancer and caused by variants in the DICER1
GeneName: DICER1 PMCID: PMC7859642 HGNCID: Unavailable Inheritance Pattern: Autosomal dominant. Disease Entity: Familial pleuropulmonary blastoma (PPB), cervix embryonal rhabdomyosarcoma, multinodular goiter, nasal chondromesenchymal hemartoma, Ciliary body medulloepithelioma, Sertoli-Leydig Cell Tumor (SLCT), differentiated thyroid carcinoma, pituitary blastoma, pineoblastoma, cystic nephroma, Wilm's tumor and sarcomas of different sites including, amongst others, the uterine cervix, kidney and brain. Mutation: Germline Zygosity: Heterozygose Variant: No ClinVarID present. Family Information: No family outline Case: No specified information of patients included. CasePresentingHPO's: n/a CasePrevious Testing: n/a gnomAD: n/a Mutation Type: nonsense, frameshift, or splice affected.
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DICER1 syndrome is a rare genetic condition predisposing to hereditary cancer and caused by variants in the DICER1 gene.
GeneName: DICER1 PMID: 33552988 HGNCID: Unavailable Inheritance Pattern: Autosomal Dominant with reduced penetrance Disease Entity: Cystic nephroma, familial pleuropulmonary blastoma (PPB), ovarian Sertoli-Leydig cell tumor (SLCT), cervix embryonal rhabdomyosarcoma, multinodular goiter, Wilms' Tumor, Ciliary body medulloepithelioma, nasal chondromesenchymal hamartoma, differentiated thyroid carcinoma, pituitary blastoma, pineoblastoma, sarcomas of different sites. Mutation: germline mutation Zygosity: heterozygous Variant: ClinVar ID not listed Family Information: No family cases listed Case: No specific case mentioned gnomAD: N/A Mutation Type: Frameshift, Nonsense mutation
Tags
- Mutation: Germline
- Nasal chondromesenchymal hemartoma
- Cervix embryonal rhabdomyosarcoma
- Zygosity: Heterozygous
- Gene:DICER1
- PMID:33552988
- Wilms'tumor
- Germline
- Sarcomas
- Differentiated thyroid carcinoma
- PPB
- PMCID: PMC7859642
- Cancer
- Wilm's tumor
- Multinodular goiter
- AutosomalDominant
- Frameshift
- SLCT
- Sertoli-Letdig Cell Tumor(SLCT)
- Ciliary body medulloepitheliomma
- Mutation type: Frameshift
- Familial pleuropulmonary blastoma (PPB)
- Nonsense
- Gene: DICER1
- Mutation type: Nonsense
- Inheritance Pattern: Autosomal dominant
Annotators
URL
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- Apr 2022
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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DICER1 syndrome is a rare genetic condition predisposing to hereditary cancer and caused by variants in the DICER1 gene.
Gene Name: DICER1 PMID:33552988 HGNCID: Unavailable Inheritance Pattern:Autosomal Dominant Disease Entity: familial pleuropulmonary blastoma (PPB),cystic nephroma, ovarian Sertoli-Leydig cell tumor (SLCT), multinodular goiter, cervix embryonal rhabdomyosarcoma, Wilms’ tumor, nasal chondromesenchymal hamartoma, ciliary body medulloepithelioma, differentiated thyroid carcinoma, pituitary blastoma, pineoblastoma, and sarcomas of different sites. Mutation: Nonsense, Frameshift<br /> Zygosity: Heterosygosity Variant:No ClinVar ID present Family Information:no diseases mentioned in family Case: no specified case in this article gnomAD: n/a Mutation type: Nonsense. frameshift
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DICER1 syndrome is a cancer-predisposing disorder caused by pathogenic variants in the DICER1 gene
Gene: DICER1 PMCID: PMC7859642 PMID: 33552988 HGNCID: Unavailable Inheritance Pattern: Autosomal Dominant Disease Entity: familial pleuropulmonary blastoma (PPB),cystic nephroma, ovarian Sertoli-Leydig cell tumor (SLCT), multinodular goiter, cervix embryonal rhabdomyosarcoma, Wilms’ tumor, nasal chondromesenchymal hamartoma, ciliary body medulloepithelioma, differentiated thyroid carcinoma, pituitary blastoma, pineoblastoma, and sarcomas of different sites. Mutation: Germline Zygosity: Heterozygosity most common Variant: ClinVarID not available Family Information: No mention of disease within family Case: No case specified GnomAD: N/A Mutation Type: Nonsense or Frameshift
Tags
- cervix embryonal rhabdomyosarcoma
- ciliary body medulloepithelioma
- sarcomas
- Inheritance Pattern: Autosomal Dominant
- FamilialPleuropulmonaryBlastoma
- Heterozygosity
- PPB
- familial pleuropulmonary blastoma
- pituitary blastoma
- nasal chondromesenchymal hamartoma
- Cancer
- AutosomalDominant
- Frameshift
- Nonsense
- CysticNephroma
- NasalChondromesenchymalHamartoma
- Wilms’ tumor
- SLCT
- Mutation: Frameshift
- multinodular goiter
- PMID:33552988
- Germline
- CancerPredisposition
- Sarcomas
- pineoblastoma
- Pediatric
- PMCID: PMC7859642
- HGNCID:Unavailable
- PMID: 33552988
- cystic nephroma
- ovarian Sertoli-Leydig cell tumor
- differentiated thyroid carcinoma
- Mutation: Nonsense
- Zygosity: Heterosygosity
- Gene: DICER1
Annotators
URL
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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Pathogenic germline variants in DICER1 underlie an autosomal dominant, pleiotropic tumor-predisposition disorder.
gene name: DICER1 PMID: 33570641 HGNCID: none inheritance pattern: autosomal dominant disease entity: benign and malignant tumors mutation: germline zygosity: heterozygous variant: none family information: none
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