GCFC2
GC-rich sequence DNA-binding factor 2
Summary
The first mRNA transcript isolated for this gene was part of an artificial chimera derived from two distinct gene transcripts and a primer used in the cloning process (see Genbank accession M29204). A positively charged amino terminus present only in the chimera was determined to bind GC-rich DNA, thus mistakenly thought to identify a transcription factor gene. [provided by RefSeq, Jul 2008]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2466747122 | 2:75,891,804 | A/C | — | uncertain significance |
| rs773732020 | 2:75,891,883 | A/G | — | uncertain significance |
| rs368712901 | 2:75,893,080 | G/A | — | uncertain significance |
| rs1477093512 | 2:75,897,301 | G/T | — | uncertain significance |
| rs144822009 | 2:75,897,331 | T/C | — | uncertain significance |
| rs140229675 | 2:75,897,347 | G/A | — | likely benign |
| rs761925299 | 2:75,899,098 | C/T | — | uncertain significance |
| rs141752962 | 2:75,899,101 | T/C | — | benign |
| rs377143656 | 2:75,900,595 | C/T | — | uncertain significance |
| rs1573055770 | 2:75,907,354 | A/G | — | uncertain significance |
| rs140271309 | 2:75,914,962 | G/A | stop gained | — |
| rs1228332356 | 2:75,915,044 | A/C | — | uncertain significance |
| rs1679893341 | 2:75,915,048 | A/G | — | uncertain significance |
| rs374515599 | 2:75,916,183 | C/T | — | uncertain significance |
| rs1558741938 | 2:75,916,220 | T/A | — | uncertain significance |
| rs375499685 | 2:75,916,237 | T/C | — | uncertain significance |
| rs781555553 | 2:75,916,298 | A/G | — | uncertain significance |
| rs568695239 | 2:75,916,309 | T/C | — | uncertain significance |
| rs1334704613 | 2:75,917,097 | T/C | — | uncertain significance |
| rs1256015956 | 2:75,917,151 | G/A | — | uncertain significance |
| rs2466862438 | 2:75,917,199 | C/T | — | uncertain significance |
| rs139984043 | 2:75,919,154 | G/A | — | uncertain significance |
| rs141804437 | 2:75,919,202 | A/C | — | uncertain significance |
| rs139346154 | 2:75,919,219 | T/C | — | likely benign |
| rs780462921 | 2:75,921,401 | T/C | — | uncertain significance |
| rs749553389 | 2:75,921,403 | A/C | — | uncertain significance |
| rs2466887505 | 2:75,921,509 | T/A | — | uncertain significance |
| rs1680213911 | 2:75,921,510 | A/T | — | uncertain significance |
| rs374711307 | 2:75,921,528 | G/A | — | uncertain significance |
| rs867889039 | 2:75,921,540 | G/C | — | uncertain significance |
| rs1680319513 | 2:75,923,380 | G/C | — | uncertain significance |
| rs2298948 | 2:75,926,565 | T/C | downstream gene variant | — |
| rs2466924783 | 2:75,928,332 | G/A | — | uncertain significance |
| rs968325168 | 2:75,929,505 | G/A | — | uncertain significance |
| rs374713738 | 2:75,929,545 | C/G | — | likely benign |
| rs2466956541 | 2:75,933,668 | T/G | — | uncertain significance |
| rs1681111818 | 2:75,937,756 | G/A | — | uncertain significance |
| rs540676907 | 2:75,937,789 | G/C | — | uncertain significance |
| rs562820871 | 2:75,937,827 | G/A | — | uncertain significance |
| rs774286809 | 2:75,937,903 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.