UTY
ubiquitously transcribed tetratricopeptide repeat containing, Y-linked
Summary
This gene encodes a protein containing tetratricopeptide repeats which are thought to be involved in protein-protein interactions. The encoded protein is also a minor histocompatibility antigen which may induce graft rejection of male stem cell grafts. A large number of alternatively spliced transcripts have been observed for this gene, but the full length nature of some of these variants has not been determined. [provided by RefSeq, Apr 2012]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9786378 | Y:15,360,167 | G/C | — | — |
| rs113965720 | Y:15,371,841 | T/C | — | — |
| rs9785890 | Y:15,375,740 | A/G | — | — |
| rs34141256 | Y:15,409,812 | G/A | — | — |
| rs111360254 | Y:15,414,257 | A/G | — | — |
| rs72625386 | Y:15,414,633 | A/T | — | — |
| rs16980601 | Y:15,415,115 | A/T | — | — |
| rs796827870 | Y:15,426,005 | C/T | — | — |
| rs547367934 | Y:15,435,514 | C/T | — | likely benign |
| rs2032667 | Y:15,436,316 | G/A | — | — |
| rs2032669 | Y:15,436,915 | T/C | — | — |
| rs2032670 | Y:15,437,050 | A/G | — | — |
| rs2032671 | Y:15,437,063 | C/T | — | — |
| rs9341279 | Y:15,437,152 | C/T | — | — |
| rs2032668 | Y:15,437,333 | A/C | — | — |
| rs2032666 | Y:15,437,564 | C/T | — | — |
| rs13447373 | Y:15,467,785 | T/A | intron variant | — |
| rs2032654 | Y:15,467,824 | A/G | synonymous variant | — |
| rs9341278 | Y:15,469,724 | G/A | intron variant | — |
| rs13447376 | Y:15,469,740 | C/A | intron variant | — |
| rs2032674 | Y:15,471,925 | T/C | — | — |
| rs113011136 | Y:15,472,586 | C/G | — | — |
| rs9786043 | Y:15,472,863 | T/C | — | — |
| rs17221922 | Y:15,479,899 | T/A | — | — |
| rs9306837 | Y:15,480,547 | G/A | — | — |
| rs9341277 | Y:15,481,372 | T/A | — | — |
| rs34486382 | Y:15,481,435 | G/T | — | — |
| rs374659297 | Y:15,498,975 | T/A | — | — |
| rs17307007 | Y:15,500,110 | A/C | — | — |
| rs112110281 | Y:15,505,259 | T/C | — | — |
| rs17221943 | Y:15,506,055 | T/C | — | — |
| rs59779827 | Y:15,510,064 | G/T | — | — |
| rs9785851 | Y:15,510,490 | C/T | — | — |
| rs9341276 | Y:15,515,812 | A/C | — | — |
| rs17221964 | Y:15,517,851 | T/G | — | — |
| rs2032664 | Y:15,526,695 | C/A | — | — |
| rs2032665 | Y:15,526,751 | C/T | — | — |
| rs2032663 | Y:15,544,614 | C/T | — | — |
| rs112810208 | Y:15,554,989 | A/G | — | — |
| rs34864948 | Y:15,574,102 | G/A | — | — |
| rs2032660 | Y:15,575,780 | A/T | — | — |
| rs2032661 | Y:15,575,790 | A/G | — | — |
| rs2032659 | Y:15,576,203 | C/T | — | — |
| rs16980558 | Y:15,579,215 | A/G | — | — |
| rs2032658 | Y:15,581,983 | G/A | intron variant | — |
| rs2032656 | Y:15,587,462 | T/G | — | — |
| rs2032657 | Y:15,587,509 | T/A | — | — |
| rs112563127 | Y:15,588,401 | T/C | — | — |
| rs17307070 | Y:15,590,342 | T/G | — | — |
| rs2072422 | Y:15,590,674 | T/A | — | — |
| rs2032655 | Y:15,591,201 | T/G | splice region variant | — |
| rs9341273 | Y:15,591,445 | T/C | missense variant | — |
| rs9341275 | Y:15,591,447 | C/T | synonymous variant | — |
| rs375296284 | Y:15,591,474 | T/G | missense variant | — |
| rs3212293 | Y:15,591,492 | C/G | missense variant | — |
| rs2032653 | Y:15,591,537 | G/C | synonymous variant | — |
| rs9785760 | Y:15,594,523 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.