CEDORA

Chr 16

CDH13 antisense oligodendrocyte and neuron associated lncRNA

Also known as: FEDORA

I apologize, but I cannot find any information about the gene "CEDORA" in standard genetic databases or medical literature. This gene symbol does not appear to correspond to a recognized human gene associated with pediatric neurological conditions. Please verify the gene symbol, as it may be a typographical error or an alternative name for a different gene.

Research

ResearchGenerating clinical summary…

Clinical Summary— CEDORA

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ClinVar Variants

5 VUS of 12 total submissions

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Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

12 submitted variants in ClinVar

ClinVar

Classification Summary

VUS5

Likely Benign1

Benign4

VUS

Likely Benign

Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

Classification	Missense + Inframe	Non-coding	Total
Pathogenic	0	0	0
Likely Pathogenic	0	0	0
VUS	5	0	5
Likely Benign	0	1	1
Benign	0	4	4
Total	5	5	10

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

23 pathogenic / likely-pathogenic (of 29) ClinVar copy-number / structural variants overlap CEDORA — these span large chromosomal regions, not the gene specifically, and are excluded from the counts above. Explore in CNV tools →