MIEN1 migration and invasion enhancer 1
Gene ID: 84299, updated on 2-Nov-2024Gene type: protein coding
Also known as: C35; ORB3; XTP4; RDX12; C17orf37
- See all available tests in GTR for this gene
- Go to complete Gene record for MIEN1
- Go to Variation Viewer for MIEN1 variants
Summary
Involved in negative regulation of apoptotic process; positive regulation of cell migration; and positive regulation of filopodium assembly. Located in cytoplasmic side of plasma membrane and cytosol. [provided by Alliance of Genome Resources, Nov 2024]
Genomic context
- Location:
- 17q12
- Sequence:
- Chromosome: 17; NC_000017.11 (39728510..39730532, complement)
- Total number of exons:
- 3
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for MIEN1 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
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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