RBMS2

RNA binding motif single stranded interacting protein 2

Summary

The protein encoded by this gene is a member of a small family of proteins which bind single stranded DNA/RNA. These proteins are characterized by the presence of two sets of ribonucleoprotein consensus sequence (RNP-CS) that contain conserved motifs, RNP1 and RNP2, originally described in RNA binding proteins, and required for DNA binding. The RBMS proteins have been implicated in such diverse functions as DNA replication, gene transcription, cell cycle progression and apoptosis. This protein was isolated by phenotypic complementation of cdc2 and cdc13 mutants of yeast and is thought to suppress cdc2 and cdc13 mutants through the induction of translation of cdc2. [provided by RefSeq, Jul 2008]

Known Variants25 total

rsidPosition (GRCh37)AllelesClassClinVar
rs269491712:56,912,864T/Cregulatory region variant—
rs101148204212:56,915,856A/G—uncertain significance
rs79926012:56,921,304G/Aintron variant—
rs293323512:56,921,418A/Gintron variant—
rs730968512:56,935,413A/Gintron variant—
rs265788812:56,938,383T/C——
rs731244112:56,941,146C/Aintron variant—
rs77354849712:56,956,225A/T—uncertain significance
rs57691016412:56,958,753G/A——
rs18903297212:56,961,940A/Tintron variant—
rs254744584412:56,962,761A/G—uncertain significance
rs254744585912:56,962,764G/C—uncertain significance
rs95979249112:56,963,689G/C—uncertain significance
rs37673009812:56,975,266C/T—uncertain significance
rs88691585412:56,975,904C/T—uncertain significance
rs76874609912:56,975,926C/G—uncertain significance
rs121674468812:56,980,634G/A—uncertain significance
rs188473881612:56,980,660G/C—uncertain significance
rs77060071412:56,980,688A/C—uncertain significance
rs14633531312:56,981,422C/T—uncertain significance
rs37594382312:56,982,088C/T—uncertain significance
rs75033351712:56,982,154T/A—uncertain significance
rs20129940212:56,982,156G/A—uncertain significance
rs159252146812:56,982,718G/C—uncertain significance
rs37724624112:56,982,720G/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.