ENTREP2 endosomal transmembrane epsin interactor 2
Gene ID: 23359, updated on 2-Nov-2024Gene type: protein coding
Also known as: TMEM228; FAM189A1
- See all available tests in GTR for this gene
- Go to complete Gene record for ENTREP2
- Go to Variation Viewer for ENTREP2 variants
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias. GeneReviews: Not available | |
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. GeneReviews: Not available |
Genomic context
- Location:
- 15q13.1
- Sequence:
- Chromosome: 15; NC_000015.10 (29117712..29675409, complement)
- Total number of exons:
- 14
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for ENTREP2 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.