Prepair 1000+
Gene: CTNS Green List (high evidence)Green List (high evidence)
Well established gene disease association.
Cystinosis is a multisystemic lysosomal storage disease resulting from a defect in cystine transport out of lysosomes. This results in cystine accumulation affecting all tissues; the eyes and kidneys are the first organs to be affected. Cell damage and organ dysfunction are heterogeneous and vary in severity and progression. Cystinosis leads to severe renal Fanconi syndrome, characterized by polyuria, polydipsia, failure to thrive, vomiting, constipation, dehydration, impaired longitudinal growth, and/or hypophosphatemic/calcipenic rickets. Corneal crystals increase with age resulting in photophobia, corneal sensitivity, and reduced visual acuity if left untreated. Very rarely, patients not treated for ocular crystals may develop corneal lesions severe enough to require a corneal transplant.
Individuals can develop endocrine, cardiovascular, and neurological involvement as well as other non-specific symptoms (e.g., gastrointestinal involvement, heat intolerance, (hypophoresis) due to cystine buildup later in life. Serious non-renal manifestations usually develop in the second decade of life.
There are three main clinical forms of the disease:
1. The most severe and common subtype is infantile nephropathic cystinosis (95% of cases) MIM#219800 - failure to thrive usually reported after first 6 months of life, corneal crystals can occur prior to 1 year of age, and ocular involvement usually after 3 years old. Without treatment, progression to end stage renal disease and death prior to 10 years old.
Subtype of this condition - Cystinosis, atypical nephropathic MIM#219800, where Fanconi syndrome and renal disease are present without additional symptoms. (PMID: 1244226).
2. Juvenile (or intermediate) nephropathic cystinosis (~3% of cases) MIM#219900 - onset ~8-10 years of age. Progression to end stage renal failure occurs later than infantile form.
3. Adult non-nephropathic (ocular) cystinosis - MIM# 219750 characterized clinically only by photophobia, absent renal disease.
Clingen has lumped 3 phenotypes into a single disease name: "Cystinosis - CTNS" - no reported evidence of differences in molecular mechanisms.
Animal model present - mouse.
Note: 57kb deletion accounts for 50% of pathogenic alleles in patients of Northern European ancestry.Created: 24 Oct 2024, 11:57 a.m. | Last Modified: 24 Oct 2024, 11:57 a.m.
Panel Version: 1.486
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Cystinosis, nephropathic MIM#219800; Cystinosis, late-onset juvenile or adolescent nephropathic MIM#219900; Cystinosis, atypical nephropathic MIM#219800
Publications
Gene: ctns has been classified as Green List (High Evidence).
Phenotypes for gene: CTNS were changed from Cystinosis, nephropathic, 219800 (3) to Cystinosis, nephropathic MIM#219800; Cystinosis, late-onset juvenile or adolescent nephropathic MIM#219900; Cystinosis, atypical nephropathic MIM#219800
Publications for gene: CTNS were set to
Tag SV/CNV tag was added to gene: CTNS.
Added phenotypes Cystinosis, nephropathic, 219800 (3) for gene: CTNS
gene: CTNS was added gene: CTNS was added to Reproductive Carrier Screen_VCGS. Sources: Mackenzie's Mission,Expert Review Green Mode of inheritance for gene: CTNS was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CTNS were set to Cystinosis, nephropathic, 219800 (3)
If promoting or demoting a gene, please provide comments to justify a decision to move it.
Genes included in a Genomics England gene panel for a rare disease category (green list) should fit the criteria A-E outlined below.
These guidelines were developed as a combination of the ClinGen DEFINITIVE evidence for a causal role of the gene in the disease(a), and the Developmental Disorder Genotype-Phenotype (DDG2P) CONFIRMED DD Gene evidence level(b) (please see the original references provided below for full details). These help provide a guideline for expert reviewers when assessing whether a gene should be on the green or the red list of a panel.
A. There are plausible disease-causing mutations(i) within, affecting or encompassing an interpretable functional region(ii) of this gene identified in multiple (>3) unrelated cases/families with the phenotype(iii).
OR
B. There are plausible disease-causing mutations(i) within, affecting or encompassing cis-regulatory elements convincingly affecting the expression of a single gene identified in multiple (>3) unrelated cases/families with the phenotype(iii).
OR
C. As definitions A or B but in 2 or 3 unrelated cases/families with the phenotype, with the addition of convincing bioinformatic or functional evidence of causation e.g. known inborn error of metabolism with mutation in orthologous gene which is known to have the relevant deficient enzymatic activity in other species; existence of an animal model which recapitulates the human phenotype.
AND
D. Evidence indicates that disease-causing mutations follow a Mendelian pattern of causation appropriate for reporting in a diagnostic setting(iv).
AND
E. No convincing evidence exists or has emerged that contradicts the role of the gene in the specified phenotype.
(i)Plausible disease-causing mutations: Recurrent de novo mutations convincingly affecting gene function. Rare, fully-penetrant mutations - relevant genotype never, or very rarely, seen in controls. (ii) Interpretable functional region: ORF in protein coding genes miRNA stem or loop. (iii) Phenotype: the rare disease category, as described in the eligibility statement. (iv) Intermediate penetrance genes should not be included.
It’s assumed that loss-of-function variants in this gene can cause the disease/phenotype unless an exception to this rule is known. We would like to collect information regarding exceptions. An example exception is the PCSK9 gene, where loss-of-function variants are not relevant for a hypercholesterolemia phenotype as they are associated with increased LDL-cholesterol uptake via LDLR (PMID: 25911073).
If a curated set of known-pathogenic variants is available for this gene-phenotype, please contact us at panelapp@genomicsengland.co.uk
We classify loss-of-function variants as those with the following Sequence Ontology (SO) terms:
Term descriptions can be found on the PanelApp homepage and Ensembl.
If you are submitting this evaluation on behalf of a clinical laboratory please indicate whether you report variants in this gene as part of your current diagnostic practice by checking the box
Standardised terms were used to represent the gene-disease mode of inheritance, and were mapped to commonly used terms from the different sources. Below each of the terms is described, along with the equivalent commonly-used terms.
A variant on one allele of this gene can cause the disease, and imprinting has not been implicated.
A variant on the paternally-inherited allele of this gene can cause the disease, if the alternate allele is imprinted (function muted).
A variant on the maternally-inherited allele of this gene can cause the disease, if the alternate allele is imprinted (function muted).
A variant on one allele of this gene can cause the disease. This is the default used for autosomal dominant mode of inheritance where no knowledge of the imprinting status of the gene required to cause the disease is known. Mapped to the following commonly used terms from different sources: autosomal dominant, dominant, AD, DOMINANT.
A variant on both alleles of this gene is required to cause the disease. Mapped to the following commonly used terms from different sources: autosomal recessive, recessive, AR, RECESSIVE.
The disease can be caused by a variant on one or both alleles of this gene. Mapped to the following commonly used terms from different sources: autosomal recessive or autosomal dominant, recessive or dominant, AR/AD, AD/AR, DOMINANT/RECESSIVE, RECESSIVE/DOMINANT.
A variant on one allele of this gene can cause the disease, however a variant on both alleles of this gene can result in a more severe form of the disease/phenotype.
A variant in this gene can cause the disease in males as they have one X-chromosome allele, whereas a variant on both X-chromosome alleles is required to cause the disease in females. Mapped to the following commonly used term from different sources: X-linked recessive.
A variant in this gene can cause the disease in males as they have one X-chromosome allele. A variant on one allele of this gene may also cause the disease in females, though the disease/phenotype may be less severe and may have a later-onset than is seen in males. X-linked inactivation and mosaicism in different tissues complicate whether a female presents with the disease, and can change over their lifetime. This term is the default setting used for X-linked genes, where it is not known definitately whether females require a variant on each allele of this gene in order to be affected. Mapped to the following commonly used terms from different sources: X-linked dominant, x-linked, X-LINKED, X-linked.
The gene is in the mitochondrial genome and variants within this can cause this disease, maternally inherited. Mapped to the following commonly used term from different sources: Mitochondrial.
Mapped to the following commonly used terms from different sources: Unknown, NA, information not provided.
For example, if the mode of inheritance is digenic, please indicate this in the comments and which other gene is involved.