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NEM6

Chr 15AD

nemaline myopathy 6

I notice that you've provided the gene name "NEM6" but no supporting data about protein function, associated diseases, inheritance patterns, or constraint metrics. According to the strict rules you've outlined, I can only use information that has been provided and cannot add claims not supported by the given data. Since no information about protein function, associated phenotypes, inheritance pattern, or other relevant details has been provided for NEM6, I cannot write a clinical summary that would meet your requirements of being evidence-based and supported by the provided data. Could you please provide the supporting information for NEM6 so I can write an appropriate clinical summary?

AD1 OMIM phenotype
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/NEM6?content-type=application/json&expand=1

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

NEM6 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

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