GIMAP1-GIMAP5
GIMAP1-GIMAP5 readthrough
Summary
This locus represents naturally occurring readthrough transcription between the neighboring GIMAP1 (GTPase, IMAP family member 1) and GIMAP5 (GTPase, IMAP family member 5) genes on chromosome 7. Alternative splicing results in multiple readthrough transcript variants, one of which encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Jan 2015]
Known Variants10 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143092565 | 7:150,425,144 | A/G | downstream gene variant | — |
| rs11765245 | 7:150,427,763 | A/C | intron variant | — |
| rs1158851604 | 7:150,434,626 | C/T | — | uncertain significance |
| rs188514147 | 7:150,434,641 | G/A | — | likely benign |
| rs1188732044 | 7:150,434,660 | G/C | — | uncertain significance |
| rs1399043118 | 7:150,434,693 | G/A | — | uncertain significance |
| rs1001318981 | 7:150,434,734 | G/A | — | uncertain significance |
| rs1797535991 | 7:150,434,775 | C/G | — | uncertain significance |
| rs2485928712 | 7:150,439,510 | G/C | — | uncertain significance |
| rs147182394 | 7:150,439,760 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.