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NEDSG

Chr 1AR

ubiquitin-fold modifier conjugating enzyme 1

Also known as: HSPC155, NEDSG

UFC1 functions as an E2-like conjugating enzyme for ubiquitin-fold modifier-1 (UFM1) in the UFMylation pathway. Autosomal recessive mutations cause neurodevelopmental disorder with spasticity and poor growth, affecting both the nervous system and somatic development.

OMIMResearchSummary from RefSeq, OMIM
AR1 OMIM phenotype
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/NEDSG?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

NEDSG · 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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Clinical Literature
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Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found