MIA3

MIA SH3 domain ER export factor 3

Summary

Enables cargo receptor activity. Involved in several processes, including COPII-coated vesicle cargo loading; cell migration involved in sprouting angiogenesis; and regulation of leukocyte migration. Located in endoplasmic reticulum exit site and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants133 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs765741608	1:222,791,496	G/A	—	uncertain significance
rs2378584	1:222,793,632	A/G	intron variant	—
rs4846384	1:222,797,614	C/G	intron variant	—
rs2527564471	1:222,798,111	T/C	—	uncertain significance
rs769464287	1:222,798,162	A/C	—	uncertain significance
rs17163313	1:222,799,625	T/G	intron variant	—
rs377438329	1:222,800,983	T/G	—	uncertain significance
rs200522371	1:222,800,987	G/A	—	uncertain significance
rs780066537	1:222,801,098	C/T	—	uncertain significance
rs1418075680	1:222,801,102	A/C	—	uncertain significance
rs2527578016	1:222,801,232	C/G	—	uncertain significance
rs2527578021	1:222,801,233	A/C	—	uncertain significance
rs184666801	1:222,801,235	G/C	—	likely benign
rs1662200964	1:222,801,409	G/T	—	uncertain significance
rs76237185	1:222,801,448	G/A	—	likely benign
rs1398062151	1:222,801,471	T/G	—	uncertain significance
rs1662211274	1:222,801,577	A/G	—	likely benign
rs370082212	1:222,801,643	G/A	—	uncertain significance
rs766885917	1:222,801,649	A/G	—	uncertain significance
rs142088763	1:222,801,661	A/T	—	benign
rs374210364	1:222,801,752	C/T	—	uncertain significance
rs757543272	1:222,801,801	A/T	—	uncertain significance
rs761103413	1:222,801,843	A/T	—	uncertain significance
rs761896540	1:222,801,872	C/T	—	uncertain significance
rs1662232580	1:222,801,890	G/C	—	uncertain significance
rs1158930648	1:222,801,892	C/G	—	uncertain significance
rs1662233468	1:222,801,919	A/C	—	uncertain significance
rs150776844	1:222,801,939	C/T	—	likely benign
rs758015715	1:222,801,940	G/T	—	uncertain significance
rs746689324	1:222,801,952	A/G	—	uncertain significance
rs2527583011	1:222,801,961	A/G	—	uncertain significance
rs371816838	1:222,801,973	G/A	—	uncertain significance
rs201688063	1:222,802,001	A/C	—	uncertain significance
rs375824764	1:222,802,037	G/A	—	uncertain significance
rs1454057022	1:222,802,099	G/C	—	uncertain significance
rs773230620	1:222,802,141	G/A	—	uncertain significance
rs759802892	1:222,802,163	A/G	—	uncertain significance
rs750127963	1:222,802,186	G/A	—	uncertain significance
rs79662083	1:222,802,243	A/C	—	uncertain significance
rs762858988	1:222,802,249	G/T	—	uncertain significance
rs377652238	1:222,802,261	A/G	—	uncertain significance
rs1662257358	1:222,802,303	C/T	—	uncertain significance
rs200100305	1:222,802,423	G/A	—	uncertain significance
rs751009650	1:222,802,481	T/G	—	uncertain significance
rs368444914	1:222,802,501	G/A	—	uncertain significance
rs1436011579	1:222,802,526	T/C	—	uncertain significance
rs770852375	1:222,802,540	G/C	—	uncertain significance
rs200420941	1:222,802,669	G/A	—	uncertain significance
rs752819054	1:222,802,697	G/A	—	likely benign
rs376386576	1:222,802,777	G/A	—	uncertain significance
rs199979587	1:222,802,783	C/T	—	likely benign
rs3748626	1:222,802,803	T/C	synonymous variant	—
rs376170541	1:222,802,930	A/C	—	uncertain significance
rs1314390558	1:222,802,934	C/G	—	uncertain significance
rs767781465	1:222,802,937	G/A	—	likely benign
rs367936377	1:222,803,042	G/A	—	uncertain significance
rs1571868123	1:222,803,060	G/C	—	uncertain significance
rs76329326	1:222,803,199	C/A	—	likely benign
rs756693626	1:222,803,225	G/T	—	uncertain significance
rs374709745	1:222,803,257	C/G	—	uncertain significance
rs372579977	1:222,803,290	A/G	—	uncertain significance
rs75351629	1:222,803,332	C/A	—	uncertain significance
rs775717454	1:222,803,361	A/T	—	uncertain significance
rs1269633661	1:222,803,399	A/T	—	uncertain significance
rs2527593443	1:222,803,415	G/T	—	uncertain significance
rs200919201	1:222,803,457	G/C	—	uncertain significance
rs200475811	1:222,803,465	C/G	—	uncertain significance
rs374881779	1:222,803,531	C/A	—	uncertain significance
rs527835375	1:222,803,552	G/A	—	uncertain significance
rs935449524	1:222,803,683	C/G	—	uncertain significance
rs3008621	1:222,804,046	G/A	intron variant	—
rs376716496	1:222,806,511	G/T	—	uncertain significance
rs577679209	1:222,806,514	G/A	—	uncertain significance
rs1002440523	1:222,806,521	C/T	—	uncertain significance
rs778168637	1:222,806,527	G/A	—	uncertain significance
rs751969769	1:222,806,547	G/A	—	uncertain significance
rs377488250	1:222,806,573	G/A	—	likely benign
rs35700460	1:222,811,407	A/C	—	—
rs575246690	1:222,818,905	A/G	—	uncertain significance
rs201684121	1:222,818,925	G/T	—	uncertain significance
rs2527656857	1:222,818,968	A/G	—	uncertain significance
rs17163360	1:222,820,790	T/C	—	—
rs771534699	1:222,822,182	A/G	—	pathogenic
rs28709375	1:222,822,999	A/T	—	—
rs17465637	1:222,823,529	A/G	—	benign
rs374910596	1:222,823,637	C/T	—	uncertain significance
rs67180937	1:222,823,743	T/C	—	—
rs771104439	1:222,824,210	T/C	—	uncertain significance
rs2124907107	1:222,825,334	A/G	—	uncertain significance
rs768770008	1:222,825,582	C/G	—	uncertain significance
rs752355280	1:222,825,608	G/C	—	uncertain significance
rs10495198	1:222,825,717	T/C	intron variant	—
rs1459201213	1:222,826,414	T/C	—	uncertain significance
rs1663525836	1:222,826,420	A/C	—	uncertain significance
rs758504855	1:222,826,462	A/G	—	uncertain significance
rs372947244	1:222,826,625	A/C	—	uncertain significance
rs779808017	1:222,827,587	G/A	—	uncertain significance
rs770342754	1:222,827,632	G/A	—	likely benign
rs776000491	1:222,827,636	C/T	—	uncertain significance
rs763350411	1:222,827,638	C/T	—	uncertain significance

Showing 100 of 133 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.