MROH2B
maestro heat like repeat family member 2B
Summary
Predicted to be involved in protein kinase A signaling. Predicted to be located in sperm midpiece. Predicted to be active in acrosomal vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants97 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs777067776 | 5:40,998,161 | G/A | — | uncertain significance |
| rs376560865 | 5:40,998,234 | A/G | — | uncertain significance |
| rs1479019110 | 5:40,998,238 | A/T | — | uncertain significance |
| rs1346979998 | 5:40,998,719 | G/T | — | uncertain significance |
| rs1321942948 | 5:40,999,781 | G/A | — | uncertain significance |
| rs200489389 | 5:40,999,799 | C/T | — | uncertain significance |
| rs1376175 | 5:40,999,900 | T/G | — | — |
| rs200676167 | 5:41,000,334 | G/T | — | uncertain significance |
| rs189708836 | 5:41,000,383 | C/T | — | likely benign |
| rs199554682 | 5:41,000,392 | A/G | — | uncertain significance |
| rs1208128072 | 5:41,000,398 | T/C | — | uncertain significance |
| rs199956857 | 5:41,000,405 | C/T | — | uncertain significance |
| rs920158035 | 5:41,000,434 | A/T | — | uncertain significance |
| rs367639574 | 5:41,000,446 | C/T | — | uncertain significance |
| rs780611554 | 5:41,000,791 | T/C | — | uncertain significance |
| rs185230674 | 5:41,000,795 | G/T | — | uncertain significance |
| rs549836281 | 5:41,000,843 | T/G | — | uncertain significance |
| rs756512493 | 5:41,000,867 | C/A | — | uncertain significance |
| rs753433063 | 5:41,004,506 | C/T | — | uncertain significance |
| rs538838769 | 5:41,004,594 | T/C | — | uncertain significance |
| rs767562629 | 5:41,004,938 | C/A | — | uncertain significance |
| rs1275923036 | 5:41,004,978 | A/T | — | uncertain significance |
| rs141655634 | 5:41,005,699 | C/T | — | likely benign |
| rs2478361534 | 5:41,007,530 | A/G | — | uncertain significance |
| rs369303264 | 5:41,008,757 | G/A | — | uncertain significance |
| rs185546559 | 5:41,008,848 | G/A | — | likely benign |
| rs377601534 | 5:41,009,410 | T/C | — | uncertain significance |
| rs758914803 | 5:41,009,479 | G/T | — | uncertain significance |
| rs753325044 | 5:41,010,080 | G/C | — | uncertain significance |
| rs368383392 | 5:41,010,091 | G/C | — | uncertain significance |
| rs79005885 | 5:41,010,097 | T/A | — | uncertain significance |
| rs200620715 | 5:41,012,710 | T/C | — | uncertain significance |
| rs775728964 | 5:41,012,713 | T/A | — | uncertain significance |
| rs2478379762 | 5:41,012,714 | T/C | — | uncertain significance |
| rs778601034 | 5:41,012,756 | T/C | — | uncertain significance |
| rs1446286113 | 5:41,012,779 | T/C | — | uncertain significance |
| rs369668286 | 5:41,012,780 | C/G | — | uncertain significance |
| rs1158077009 | 5:41,015,488 | C/A | — | uncertain significance |
| rs896065939 | 5:41,015,533 | C/T | — | uncertain significance |
| rs1224550050 | 5:41,015,553 | T/G | — | uncertain significance |
| rs199545321 | 5:41,017,990 | G/A | — | uncertain significance |
| rs371175759 | 5:41,018,030 | C/T | — | uncertain significance |
| rs1742039697 | 5:41,018,803 | T/A | — | uncertain significance |
| rs201612500 | 5:41,019,002 | C/T | — | uncertain significance |
| rs62357111 | 5:41,027,653 | G/T | intron variant | — |
| rs774710073 | 5:41,032,857 | T/C | — | uncertain significance |
| rs761267578 | 5:41,032,869 | C/T | — | uncertain significance |
| rs202160588 | 5:41,032,898 | T/C | — | uncertain significance |
| rs751187629 | 5:41,032,899 | C/A | — | uncertain significance |
| rs2478458739 | 5:41,032,915 | A/C | — | uncertain significance |
| rs1742630663 | 5:41,033,208 | C/G | — | uncertain significance |
| rs747589741 | 5:41,033,216 | C/T | — | uncertain significance |
| rs201372772 | 5:41,033,245 | C/A | — | uncertain significance |
| rs1014284698 | 5:41,033,943 | G/C | — | uncertain significance |
| rs368234466 | 5:41,038,873 | A/G | — | uncertain significance |
| rs372870181 | 5:41,038,876 | T/G | — | uncertain significance |
| rs202211129 | 5:41,038,918 | C/T | — | uncertain significance |
| rs750019046 | 5:41,039,557 | C/T | — | uncertain significance |
| rs751117880 | 5:41,039,564 | T/C | — | uncertain significance |
| rs372978038 | 5:41,039,611 | A/G | — | uncertain significance |
| rs776536771 | 5:41,039,631 | A/C | — | uncertain significance |
| rs370962710 | 5:41,042,236 | C/G | — | uncertain significance |
| rs200631985 | 5:41,042,274 | A/G | — | uncertain significance |
| rs1327516481 | 5:41,042,291 | A/G | — | uncertain significance |
| rs374944474 | 5:41,045,865 | T/G | — | uncertain significance |
| rs761503056 | 5:41,045,888 | T/C | — | uncertain significance |
| rs201687257 | 5:41,048,434 | G/C | — | uncertain significance |
| rs750729220 | 5:41,048,471 | C/T | — | uncertain significance |
| rs756584525 | 5:41,048,474 | C/A | — | uncertain significance |
| rs199537835 | 5:41,048,477 | A/G | — | likely benign |
| rs1379523439 | 5:41,051,120 | C/T | — | uncertain significance |
| rs1451531573 | 5:41,051,162 | T/A | — | uncertain significance |
| rs2478526719 | 5:41,051,179 | T/C | — | uncertain significance |
| rs373485768 | 5:41,052,583 | G/A | — | likely benign |
| rs185312266 | 5:41,052,617 | G/A | — | uncertain significance |
| rs753051490 | 5:41,052,629 | G/A | — | uncertain significance |
| rs540024081 | 5:41,052,637 | A/G | — | uncertain significance |
| rs774059836 | 5:41,057,232 | A/T | — | uncertain significance |
| rs772775000 | 5:41,057,251 | C/T | — | likely benign |
| rs370738850 | 5:41,057,395 | G/T | — | uncertain significance |
| rs200696573 | 5:41,057,417 | G/C | — | uncertain significance |
| rs200045457 | 5:41,057,426 | C/T | — | uncertain significance |
| rs762785601 | 5:41,058,241 | C/T | — | uncertain significance |
| rs368563285 | 5:41,058,253 | C/T | — | uncertain significance |
| rs758302074 | 5:41,061,745 | C/G | — | uncertain significance |
| rs2478568789 | 5:41,064,594 | A/G | — | uncertain significance |
| rs200448809 | 5:41,064,643 | T/C | — | uncertain significance |
| rs1350609394 | 5:41,064,664 | T/C | — | uncertain significance |
| rs371197953 | 5:41,064,672 | A/G | — | uncertain significance |
| rs1307358470 | 5:41,065,543 | G/A | — | uncertain significance |
| rs376622338 | 5:41,065,573 | A/C | — | uncertain significance |
| rs1188361897 | 5:41,067,223 | A/G | — | uncertain significance |
| rs1743837068 | 5:41,067,235 | G/C | — | uncertain significance |
| rs745529547 | 5:41,067,241 | T/C | — | uncertain significance |
| rs1230632961 | 5:41,067,250 | C/T | — | likely benign |
| rs139046598 | 5:41,067,259 | A/G | — | likely benign |
| rs1276104927 | 5:41,069,822 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.