Data Sharing Resources
GenomeConnect
Events
Contact
Toggle navigation
Navigation
Get Started
About Us
Curation Activities
Gene-Disease Validity
Training Materials
Browse Curations
Variant Pathogenicity
Training Materials
Browse Curations
Clinical Actionability
Training Materials
Browse Curations
Dosage Sensitivity
Training Materials
Browse Curations
Browse All ClinGen's Curated Genes
Working Groups
Expert Panels
Documents
& Announcements
Tools
Search:
Gene
Gene
Disease
Variant
Website Search
Browse Curations
About ClinGen's Curation Activities
Browse
All Curated Genes
Browse
Gene-Disease Validity
Browse
Dosage Sensitivity
Browse
Clinical Actionability
Browse
Variant Pathogenicity
SYNE4
Name
SYNE4
HGNC ID
HGNC:26703
Cytogenetic Location
19q13.12
Haploinsufficiency
Associated with Autosomal Recessive Phenotype
Triplosensitivity
No Evidence
External Resources
View external resources
ClinVar Variants
View ClinVar Variants
GeneReviews®
View GeneReviews
ClinGen's Curation Summaries
External Genomic Resources
ClinVar Variants
SYNE4
-
nonsyndromic genetic deafness
| MONDO:0019497
Curated by
Classification
Date
Report
Gene-Disease Validity
Moderate
09/08/2017
View report
SYNE4
-
autosomal recessive nonsyndromic deafness 76
| MONDO:0014237
Curated by
Classification
Date
Report
Gene Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
10/16/2018
View report
SYNE4
Curated by
Classification
Date
Report
Gene Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
10/16/2018
View report
Gene Dosage Sensitivity
No Evidence for Triplosensitivity
10/16/2018
View report
Send Feedback