TRIM37

tripartite motif containing 37

Summary

This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. Mutations in this gene are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. TRIM37 localizes in peroxisomal membranes, and has been implicated in human peroxisomal biogenesis disorders. [provided by RefSeq, Jul 2020]

Known Variants612 total

rsidPosition (GRCh37)AllelesClassClinVar
rs156790370617:57,060,284T/A—likely pathogenic
rs7331721417:57,060,306C/T—likely benign
rs1245158117:57,075,654G/A—uncertain significance
rs203321100317:57,075,678G/C—uncertain significance
rs18638900517:57,075,708A/G—uncertain significance
rs100576060417:57,075,709T/C—uncertain significance
rs91417:57,075,713T/C—uncertain significance
rs102128674317:57,075,775T/C—uncertain significance
rs382635417:57,075,777T/C—uncertain significance
rs76413192317:57,075,813C/A—uncertain significance
rs14211174517:57,075,902T/C—uncertain significance
rs19170220417:57,075,979A/G—likely benign
rs18639571517:57,076,075A/G—uncertain significance
rs55301267017:57,076,080T/C—likely benign
rs2847540917:57,076,104T/A—benign
rs88605317217:57,076,116A/G—uncertain significance
rs92681378817:57,076,140G/A—uncertain significance
rs134996316917:57,076,144T/C—uncertain significance
rs18220856517:57,076,254C/T—uncertain significance
rs88605317317:57,076,357A/G—uncertain significance
rs14597395517:57,076,365T/C—benign
rs37518219717:57,076,369G/A—uncertain significance
rs88605317417:57,076,394C/T—uncertain significance
rs77955553217:57,076,503C/T—uncertain significance
rs14211354317:57,076,566G/A—uncertain significance
rs74861082117:57,076,620C/A—uncertain significance
rs37728228217:57,076,750A/G—likely benign
rs203337664817:57,076,759T/C—likely benign
rs75869750317:57,076,763T/C—uncertain significance
rs36845566417:57,076,765G/A—likely benign
rs76931336317:57,076,771G/A—likely benign
rs77436078017:57,076,784C/T—uncertain significance
rs95665744917:57,076,798A/G—likely benign
rs75949007017:57,076,799T/C—uncertain significance
rs77184678817:57,076,804A/G—likely benign
rs14968400917:57,076,809T/G—uncertain significance
rs134389138517:57,076,810G/A—likely benign
rs121303368217:57,076,817G/A—uncertain significance
rs144370161517:57,076,824T/C—likely benign
rs77674861017:57,076,830A/C—likely benign
rs254460590017:57,076,832A/C—likely benign
rs128225132217:57,076,839T/C—likely benign
rs131505144317:57,076,840A/T—likely benign
rs459897017:57,076,893T/A—benign
rs14808926217:57,078,891A/C—likely benign
rs133047633017:57,078,943A/G—likely benign
rs254466297917:57,078,944C/T—likely benign
rs76893502817:57,078,947C/T—likely benign
rs120625591917:57,078,963A/G—likely benign
rs76525227917:57,078,966C/G—likely benign
rs203378073617:57,078,969G/T—likely benign
rs254466482517:57,078,987G/A—likely benign
rs37543756617:57,078,995C/A—uncertain significance
rs56016655217:57,078,996G/A—likely benign
rs75841831617:57,079,005G/A—likely benign
rs254466608117:57,079,008C/T—likely benign
rs74682685217:57,079,017A/G—conflicting classifications of pathogenicity
rs52778942617:57,079,025C/T—uncertain significance
rs92163406417:57,079,029C/T—likely benign
rs74841966717:57,079,038C/T—likely benign
rs147656945217:57,079,041A/G—likely benign
rs137673767917:57,079,044G/A—likely benign
rs77335071817:57,079,056G/A—likely benign
rs254466807017:57,079,062G/A—likely benign
rs37609466417:57,079,064C/T—uncertain significance
rs77148500817:57,079,065G/A—likely benign
rs77467722917:57,079,066C/G—uncertain significance
rs76520327417:57,079,071C/T—uncertain significance
rs88603944517:57,079,077T/C—pathogenic
rs19224103417:57,089,571T/C—benign
rs57661226417:57,089,669A/G—likely benign
rs76352993117:57,089,673G/A—likely benign
rs121597706817:57,089,678T/C—uncertain significance
rs77269975617:57,089,679C/G—likely benign
rs254487850317:57,089,680A/C—likely benign
rs203538771317:57,089,688C/T—likely pathogenic
rs203538832917:57,089,695C/T—uncertain significance
rs203538866917:57,089,696A/G—likely benign
rs147110710517:57,089,705T/C—likely benign
rs115678383117:57,089,706G/A—uncertain significance
rs88605317517:57,089,708A/C—uncertain significance
rs254488013217:57,089,713C/A—pathogenic
rs254488069517:57,089,729C/G—uncertain significance
rs78109646517:57,089,755T/C—uncertain significance
rs77807529017:57,089,761A/T—uncertain significance
rs134658894117:57,089,767T/C—uncertain significance
rs74951875117:57,089,776G/A—likely benign
rs254488261817:57,089,780T/C—likely benign
rs141793954217:57,089,783C/T—likely benign
rs129843477617:57,089,784A/G—uncertain significance
rs254488353117:57,089,804A/G—likely benign
rs19969400117:57,089,814G/C—likely benign
rs74740895217:57,089,816A/G—likely benign
rs76909345817:57,089,822C/T—likely benign
rs254488412817:57,089,823A/C—likely benign
rs254488418817:57,089,826T/G—likely benign
rs3437029217:57,092,725G/C—benign
rs3455028217:57,092,788G/A—benign
rs14112369217:57,092,894G/A—likely benign
rs97083284517:57,092,951T/A—likely benign

Showing 100 of 612 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.