NIBAN2
niban apoptosis regulator 2
Summary
Enables transcription coactivator activity. Involved in several processes, including gonadotropin secretion; negative regulation of apoptotic process; and regulation of nucleobase-containing compound metabolic process. Located in several cellular components, including adherens junction; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138757858 | 9:130,269,249 | C/A | — | uncertain significance |
| rs144973598 | 9:130,269,278 | G/A | — | uncertain significance |
| rs368592407 | 9:130,269,287 | G/A | — | uncertain significance |
| rs548335804 | 9:130,269,306 | C/T | — | uncertain significance |
| rs757794622 | 9:130,269,315 | G/A | — | uncertain significance |
| rs2539484473 | 9:130,269,414 | T/C | — | uncertain significance |
| rs552467244 | 9:130,269,425 | G/A | — | uncertain significance |
| rs762228282 | 9:130,269,434 | G/A | — | uncertain significance |
| rs574662860 | 9:130,269,513 | G/A | — | uncertain significance |
| rs745760357 | 9:130,269,515 | C/T | — | uncertain significance |
| rs368668074 | 9:130,269,527 | G/A | — | uncertain significance |
| rs201626107 | 9:130,269,576 | C/T | — | uncertain significance |
| rs768241453 | 9:130,269,612 | C/T | — | uncertain significance |
| rs999847409 | 9:130,269,693 | C/G | — | uncertain significance |
| rs1588149264 | 9:130,270,209 | T/A | — | uncertain significance |
| rs1836649117 | 9:130,270,428 | G/C | — | uncertain significance |
| rs1216080262 | 9:130,270,430 | G/A | — | uncertain significance |
| rs1419855882 | 9:130,270,473 | C/T | — | uncertain significance |
| rs1246109495 | 9:130,270,736 | T/G | — | uncertain significance |
| rs749442375 | 9:130,270,802 | C/T | — | uncertain significance |
| rs781775048 | 9:130,271,340 | G/A | — | uncertain significance |
| rs371866914 | 9:130,271,355 | T/C | — | uncertain significance |
| rs2539491051 | 9:130,271,409 | T/A | — | uncertain significance |
| rs140423692 | 9:130,272,445 | C/T | — | uncertain significance |
| rs1414408132 | 9:130,272,533 | C/G | — | uncertain significance |
| rs772398032 | 9:130,272,601 | G/C | — | uncertain significance |
| rs141392004 | 9:130,279,168 | G/T | — | uncertain significance |
| rs371085080 | 9:130,279,183 | A/G | — | uncertain significance |
| rs1464587213 | 9:130,279,184 | T/C | — | uncertain significance |
| rs2539506186 | 9:130,279,211 | C/T | — | uncertain significance |
| rs756382989 | 9:130,279,248 | G/A | — | likely benign |
| rs139210254 | 9:130,279,268 | C/T | — | uncertain significance |
| rs150543761 | 9:130,279,404 | C/T | — | uncertain significance |
| rs567489926 | 9:130,279,437 | G/A | — | uncertain significance |
| rs949854154 | 9:130,279,438 | G/A | — | uncertain significance |
| rs1490814073 | 9:130,280,143 | A/G | — | uncertain significance |
| rs758013461 | 9:130,280,187 | G/A | — | uncertain significance |
| rs773593282 | 9:130,285,973 | G/A | — | uncertain significance |
| rs1422592360 | 9:130,285,982 | C/G | — | uncertain significance |
| rs144153796 | 9:130,286,015 | C/T | — | uncertain significance |
| rs559492611 | 9:130,286,047 | G/A | — | uncertain significance |
| rs1235501532 | 9:130,286,096 | T/C | — | uncertain significance |
| rs141182179 | 9:130,286,118 | C/A | — | likely benign |
| rs1891732 | 9:130,286,428 | G/A | intron variant | — |
| rs1019088353 | 9:130,287,391 | T/G | — | uncertain significance |
| rs375126632 | 9:130,287,432 | C/T | — | uncertain significance |
| rs762857729 | 9:130,287,438 | T/C | — | uncertain significance |
| rs527792182 | 9:130,289,474 | G/A | — | likely benign |
| rs370720142 | 9:130,289,499 | C/T | — | uncertain significance |
| rs549746967 | 9:130,289,525 | C/T | — | uncertain significance |
| rs764587574 | 9:130,289,546 | T/A | — | uncertain significance |
| rs368490986 | 9:130,289,573 | G/A | — | uncertain significance |
| rs374845565 | 9:130,289,582 | A/G | — | uncertain significance |
| rs182478049 | 9:130,289,588 | T/G | — | uncertain significance |
| rs1837186746 | 9:130,293,995 | G/C | — | uncertain significance |
| rs777969730 | 9:130,294,049 | C/T | — | uncertain significance |
| rs139344456 | 9:130,294,054 | T/G | — | uncertain significance |
| rs2249101 | 9:130,330,036 | A/T | — | — |
| rs1406756070 | 9:130,331,120 | C/A | — | uncertain significance |
| rs893290433 | 9:130,331,141 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.