MSTO1

misato mitochondrial distribution and morphology regulator 1

Summary

Involved in mitochondrion distribution; mitochondrion organization; and positive regulation of mitochondrial fusion. Located in mitochondrial outer membrane. Is active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants149 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs184021977	1:155,536,318	C/T	upstream gene variant	—
rs12030596	1:155,536,437	A/G	upstream gene variant	—
rs8179271	1:155,536,738	G/A	upstream gene variant	—
rs139932136	1:155,538,489	A/C	downstream gene variant	—
rs537115525	1:155,572,575	T/C	—	—
rs116421560	1:155,579,780	C/T	—	benign
rs412421	1:155,579,831	C/T	—	benign
rs993415179	1:155,579,835	A/G	—	benign
rs955399709	1:155,580,040	A/C	—	likely pathogenic
rs141537147	1:155,580,053	C/T	—	likely benign
rs762798018	1:155,580,061	G/A	missense variant	pathogenic
rs1673537653	1:155,580,073	C/G	—	uncertain significance
rs926774989	1:155,580,083	A/G	—	uncertain significance
rs757329280	1:155,580,090	C/G	—	likely benign
rs1235749181	1:155,580,104	C/A	—	likely pathogenic
rs1673545403	1:155,580,118	C/T	—	pathogenic
rs1233923647	1:155,580,228	G/C	—	uncertain significance
rs1673617254	1:155,580,231	C/T	—	pathogenic
rs1006121390	1:155,580,244	C/G	—	uncertain significance
rs553985742	1:155,580,252	C/A	—	benign
rs1191380112	1:155,580,259	G/C	—	uncertain significance
rs2525401371	1:155,580,285	C/A	—	uncertain significance
rs2525401822	1:155,580,319	A/C	—	uncertain significance
rs1187504822	1:155,580,356	G/C	—	conflicting classifications of pathogenicity
rs2525409709	1:155,580,871	G/T	—	uncertain significance
rs780450828	1:155,580,889	G/A	—	uncertain significance
rs146175548	1:155,581,009	A/G	—	conflicting classifications of pathogenicity
rs1673888548	1:155,581,016	G/C	—	uncertain significance
rs770531437	1:155,581,021	C/T	—	uncertain significance
rs150529804	1:155,581,038	C/T	—	benign
rs533491778	1:155,581,053	C/G	—	uncertain significance
rs781637955	1:155,581,083	G/C	—	likely pathogenic
rs71628674	1:155,581,311	T/C	—	benign
rs1417067430	1:155,581,343	G/A	—	uncertain significance
rs1674068522	1:155,581,368	G/A	—	uncertain significance
rs2148988026	1:155,581,477	C/G	—	uncertain significance
rs770785261	1:155,581,500	G/A	—	likely benign
rs1294800991	1:155,581,501	C/T	—	uncertain significance
rs533664518	1:155,581,547	C/G	—	likely benign
rs1185376088	1:155,581,581	C/T	—	uncertain significance
rs1351785077	1:155,581,618	G/A	—	uncertain significance
rs1200697	1:155,581,757	A/G	—	benign
rs777651549	1:155,581,784	C/T	—	uncertain significance
rs2525425224	1:155,581,792	G/A	—	likely benign
rs199622059	1:155,581,850	G/A	—	uncertain significance
rs2148989477	1:155,581,860	A/G	—	uncertain significance
rs2525426008	1:155,581,861	T/G	—	uncertain significance
rs776826330	1:155,581,864	C/G	—	conflicting classifications of pathogenicity
rs748305427	1:155,581,866	A/T	—	uncertain significance
rs1208636573	1:155,581,889	C/T	—	likely pathogenic
rs200355734	1:155,581,953	T/C	—	likely benign
rs1477047792	1:155,581,962	C/A	—	likely benign
rs112951003	1:155,581,966	C/T	—	likely benign
rs114719996	1:155,581,967	G/A	—	benign
rs470548	1:155,581,968	T/C	—	benign
rs763812515	1:155,581,994	C/G	—	uncertain significance
rs753488873	1:155,582,000	G/C	—	pathogenic
rs1674285118	1:155,582,001	A/G	—	uncertain significance
rs2525429699	1:155,582,002	T/C	—	likely benign
rs1256630555	1:155,582,003	G/A	—	uncertain significance
rs764871960	1:155,582,010	C/A	—	conflicting classifications of pathogenicity
rs368293868	1:155,582,019	G/A	—	uncertain significance
rs1475082174	1:155,582,021	G/A	—	uncertain significance
rs778044331	1:155,582,026	G/C	—	uncertain significance
rs145633919	1:155,582,029	G/A	—	likely benign
rs367885512	1:155,582,060	C/G	—	uncertain significance
rs565781618	1:155,582,061	G/A	—	uncertain significance
rs1674307094	1:155,582,066	A/G	—	uncertain significance
rs423975	1:155,582,074	C/T	—	likely benign
rs1296920523	1:155,582,095	C/T	—	likely benign
rs1362950816	1:155,582,097	A/G	—	uncertain significance
rs1401119828	1:155,582,098	C/T	—	likely benign
rs74603138	1:155,582,104	T/A	—	benign
rs1288230877	1:155,582,121	A/G	—	likely benign
rs150293691	1:155,582,123	A/C	—	benign
rs779235092	1:155,582,124	G/A	—	likely benign
rs746213150	1:155,582,126	A/G	—	uncertain significance
rs1319550733	1:155,582,205	C/T	—	likely benign
rs2525436702	1:155,582,211	G/A	—	uncertain significance
rs143029385	1:155,582,228	A/G	—	likely benign
rs563943670	1:155,582,231	G/A	—	pathogenic
rs777399476	1:155,582,256	C/T	—	likely benign
rs137896859	1:155,582,257	G/A	—	likely benign
rs369915310	1:155,582,270	C/T	—	uncertain significance
rs759414031	1:155,582,279	C/T	—	uncertain significance
rs1291901635	1:155,582,290	C/A	—	uncertain significance
rs1674418791	1:155,582,293	T/G	—	uncertain significance
rs765337553	1:155,582,301	G/T	—	uncertain significance
rs751943144	1:155,582,315	G/T	—	uncertain significance
rs140753725	1:155,582,325	C/T	—	likely benign
rs149058840	1:155,582,326	G/A	—	conflicting classifications of pathogenicity
rs777210932	1:155,582,339	G/A	—	likely benign
rs771965165	1:155,582,362	G/A	splice region variant	pathogenic
rs200849222	1:155,582,380	G/T	—	benign
rs768686448	1:155,582,632	C/T	—	likely benign
rs622288	1:155,582,639	C/T	missense variant	pathogenic
rs2525447351	1:155,582,657	G/A	—	uncertain significance
rs1236444491	1:155,582,664	C/A	—	likely benign
rs757761857	1:155,582,689	A/G	—	uncertain significance
rs764746264	1:155,582,692	G/A	—	uncertain significance

Showing 100 of 149 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.