IQCE

IQ motif containing E

Summary

Involved in limb morphogenesis. Predicted to be located in cytoplasmic side of plasma membrane. Predicted to be part of plasma membrane protein complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants127 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1780725652	7:2,598,814	C/T	—	likely benign
rs1298717770	7:2,598,818	G/A	—	likely pathogenic
rs868763422	7:2,606,777	T/C	—	uncertain significance
rs199648730	7:2,608,628	C/T	—	uncertain significance
rs61736920	7:2,611,241	A/G	—	benign
rs368265748	7:2,611,278	C/T	—	likely benign
rs751926494	7:2,611,838	A/T	—	uncertain significance
rs11976972	7:2,611,867	C/A	—	benign
rs2917751	7:2,611,878	C/T	—	benign
rs546809382	7:2,611,882	G/A	—	uncertain significance
rs751939600	7:2,611,888	G/A	—	likely benign
rs61736333	7:2,611,890	C/T	—	benign
rs755752357	7:2,611,891	G/A	—	likely benign
rs147584030	7:2,611,908	G/C	—	benign
rs370278948	7:2,611,922	G/A	—	uncertain significance
rs1447579496	7:2,611,954	A/G	—	uncertain significance
rs2304540	7:2,613,042	C/G	—	benign
rs755938967	7:2,613,051	G/A	splice region variant	pathogenic
rs2533971497	7:2,613,061	C/A	—	uncertain significance
rs61739566	7:2,613,062	T/C	—	benign
rs778453815	7:2,613,089	A/C	—	uncertain significance
rs62442626	7:2,613,133	G/A	—	benign
rs555990190	7:2,617,916	C/T	—	uncertain significance
rs976202890	7:2,617,928	G/T	—	uncertain significance
rs775507705	7:2,617,984	A/G	—	uncertain significance
rs188929365	7:2,617,988	G/A	—	uncertain significance
rs992302308	7:2,618,154	C/T	—	likely benign
rs367853752	7:2,622,273	C/T	—	likely benign
rs1782767536	7:2,622,282	C/G	—	uncertain significance
rs182671518	7:2,623,271	C/G	—	conflicting classifications of pathogenicity
rs2534054923	7:2,623,293	A/G	—	uncertain significance
rs1422684504	7:2,623,300	A/G	—	uncertain significance
rs13242369	7:2,623,351	G/A	—	benign
rs186728649	7:2,623,353	G/A	—	benign
rs7786703	7:2,623,881	C/G	—	benign
rs983215787	7:2,623,903	G/A	—	uncertain significance
rs61757091	7:2,623,911	C/T	—	benign
rs1288335679	7:2,623,913	G/C	—	uncertain significance
rs2257285	7:2,625,838	C/T	—	benign
rs191503365	7:2,625,848	G/A	—	benign
rs770196675	7:2,625,852	G/A	—	uncertain significance
rs199981463	7:2,625,866	C/T	—	likely benign
rs1201249752	7:2,625,882	A/T	—	uncertain significance
rs61736928	7:2,625,896	C/T	—	benign
rs756868544	7:2,625,913	G/A	—	uncertain significance
rs770348134	7:2,625,931	C/T	—	uncertain significance
rs2534077468	7:2,625,938	G/C	—	uncertain significance
rs749693208	7:2,625,943	A/T	—	uncertain significance
rs1345250982	7:2,625,955	A/G	—	uncertain significance
rs78104931	7:2,625,966	C/T	—	benign
rs369371411	7:2,627,480	G/A	—	uncertain significance
rs190428306	7:2,627,489	G/A	—	benign
rs768583040	7:2,627,491	C/T	—	uncertain significance
rs750214898	7:2,627,492	G/T	—	uncertain significance
rs2534108558	7:2,629,561	C/G	—	uncertain significance
rs61736917	7:2,629,607	T/C	—	benign
rs180961841	7:2,629,644	G/T	—	likely benign
rs999470909	7:2,629,652	C/T	—	uncertain significance
rs79515981	7:2,629,660	G/A	—	benign
rs1305523802	7:2,629,667	G/A	—	uncertain significance
rs113614660	7:2,629,671	G/A	—	benign
rs369745813	7:2,629,675	C/G	—	likely benign
rs377481463	7:2,629,683	C/T	—	uncertain significance
rs186163271	7:2,629,694	C/T	—	likely benign
rs373076945	7:2,629,706	C/T	—	uncertain significance
rs61753096	7:2,629,729	G/A	—	benign
rs201488742	7:2,629,735	G/C	—	uncertain significance
rs770102606	7:2,632,718	G/C	—	uncertain significance
rs753670589	7:2,632,744	C/T	—	conflicting classifications of pathogenicity
rs2534145146	7:2,634,524	G/C	—	uncertain significance
rs115808602	7:2,634,535	A/G	—	benign
rs1378009022	7:2,634,554	G/A	—	uncertain significance
rs184407101	7:2,634,595	G/A	—	likely benign
rs1053904628	7:2,634,605	C/T	—	uncertain significance
rs775073085	7:2,638,137	C/G	—	uncertain significance
rs201527451	7:2,638,163	C/G	—	uncertain significance
rs751600299	7:2,638,181	C/T	—	likely benign
rs75078943	7:2,638,189	C/T	—	benign
rs201141275	7:2,638,190	G/A	—	uncertain significance
rs114555800	7:2,638,191	C/T	—	benign
rs776673383	7:2,638,220	C/T	—	uncertain significance
rs1583495349	7:2,638,253	T/G	—	uncertain significance
rs1054261754	7:2,638,262	A/C	—	uncertain significance
rs1290951173	7:2,638,263	C/A	—	uncertain significance
rs371441568	7:2,644,517	G/A	—	likely benign
rs2293404	7:2,644,519	C/T	—	benign
rs201471152	7:2,644,523	G/T	—	likely benign
rs201863435	7:2,644,537	C/G	—	uncertain significance
rs370405991	7:2,644,558	G/A	—	uncertain significance
rs2534218726	7:2,644,579	A/G	—	uncertain significance
rs74809904	7:2,644,589	C/T	—	benign
rs754407471	7:2,644,605	G/A	—	likely benign
rs2293405	7:2,644,607	G/T	—	benign
rs757371119	7:2,644,623	C/G	—	uncertain significance
rs372253231	7:2,644,633	C/T	—	likely benign
rs112274087	7:2,645,522	C/T	—	likely benign
rs776206111	7:2,645,525	C/T	—	uncertain significance
rs10950797	7:2,645,526	G/A	—	benign
rs1196613352	7:2,645,544	C/T	—	likely benign
rs2293407	7:2,645,552	A/G	—	benign

Showing 100 of 127 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.