TRIM46
tripartite motif containing 46
Summary
This gene encodes a protein of the tripartite motif (TRIM) family. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. TRIM46 is reported to be involved in the proliferation of multiple types of cancer cells including lung and breast cancer. It has also been shown to control neuronal polarity and axon specification by forming uniform microtubule bundles in the axon. [provided by RefSeq, May 2022]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199784137 | 1:155,146,474 | C/A | — | uncertain significance |
| rs1217958591 | 1:155,147,876 | C/A | — | uncertain significance |
| rs1665572395 | 1:155,148,000 | G/C | — | uncertain significance |
| rs778280652 | 1:155,148,052 | C/T | — | uncertain significance |
| rs745531069 | 1:155,148,058 | G/A | — | uncertain significance |
| rs547877394 | 1:155,148,098 | C/A | — | uncertain significance |
| rs1438613159 | 1:155,148,379 | C/T | — | uncertain significance |
| rs200794260 | 1:155,148,462 | C/T | — | uncertain significance |
| rs893967243 | 1:155,148,502 | G/A | — | uncertain significance |
| rs376400786 | 1:155,149,717 | C/T | — | uncertain significance |
| rs2526806940 | 1:155,150,491 | A/C | — | uncertain significance |
| rs939722032 | 1:155,150,601 | C/T | — | uncertain significance |
| rs140277217 | 1:155,150,610 | G/A | — | uncertain significance |
| rs562410050 | 1:155,150,976 | G/A | — | uncertain significance |
| rs751306680 | 1:155,150,987 | G/A | — | uncertain significance |
| rs754712280 | 1:155,151,002 | C/T | — | uncertain significance |
| rs11264341 | 1:155,151,493 | C/G | — | — |
| rs9426886 | 1:155,151,754 | A/T | regulatory region variant | — |
| rs748469875 | 1:155,152,185 | C/G | — | uncertain significance |
| rs76872124 | 1:155,152,205 | C/T | — | benign |
| rs370747351 | 1:155,152,239 | G/A | — | uncertain significance |
| rs376526448 | 1:155,152,267 | G/A | — | uncertain significance |
| rs2526847931 | 1:155,154,331 | T/G | — | uncertain significance |
| rs757112582 | 1:155,154,345 | G/A | — | uncertain significance |
| rs202063546 | 1:155,154,352 | G/A | — | uncertain significance |
| rs763230919 | 1:155,154,360 | G/A | — | likely benign |
| rs1444724249 | 1:155,154,367 | G/A | — | uncertain significance |
| rs4971099 | 1:155,155,608 | A/G | downstream gene variant | — |
| rs998443380 | 1:155,156,397 | G/A | — | uncertain significance |
| rs771716937 | 1:155,156,488 | G/T | — | uncertain significance |
| rs2526864671 | 1:155,156,527 | T/G | — | uncertain significance |
| rs370921058 | 1:155,156,577 | A/G | — | uncertain significance |
| rs375807143 | 1:155,156,629 | G/T | — | uncertain significance |
| rs2070803 | 1:155,157,715 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.