SPDYE14

Chr 7

speedy/RINGO cell cycle regulator family member E14

Also known as: SPDYE14P

The protein is predicted to bind protein kinases, but no human diseases have been definitively associated with SPDYE14 mutations based on the available data. The inheritance pattern and pathogenic mechanisms remain unknown due to limited clinical and functional characterization.

Summary from RefSeq
Research Assistant →
0
Active trials
0
Pubs (1 yr)
13
P/LP submissions
P/LP missense
LOEUF
Mechanism
Clinical SummarySPDYE14
📋
ClinVar Variants
13 unique Pathogenic / Likely Pathogenic· 2 VUS of 15 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

15 submitted variants in ClinVar

Classification Summary

Pathogenic12
Likely Pathogenic1
VUS2
12
Pathogenic
1
Likely Pathogenic
2
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
12
Likely Pathogenic
1
VUS
2
Likely Benign
0
Benign
0
Total15

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SPDYE14 · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 1 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found