NDFIP2 Nedd4 family interacting protein 2
Gene ID: 54602, updated on 28-Oct-2024Gene type: protein coding
Also known as: N4WBP5A
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- Go to complete Gene record for NDFIP2
- Go to Variation Viewer for NDFIP2 variants
Summary
Enables WW domain binding activity. Involved in negative regulation of gene expression; negative regulation of transport; and positive regulation of protein ubiquitination. Located in several cellular components, including Golgi apparatus; mitochondrion; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Oct 2024]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies. GeneReviews: Not available | |
Genome-wide association study of pancreatic cancer in Japanese population. GeneReviews: Not available |
Genomic context
- Location:
- 13q31.1
- Sequence:
- Chromosome: 13; NC_000013.11 (79481155..79556077)
- Total number of exons:
- 8
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for NDFIP2 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
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