CRIM1

cysteine rich transmembrane BMP regulator 1

Summary

This gene encodes a transmembrane protein containing six cysteine-rich repeat domains and an insulin-like growth factor-binding domain. The encoded protein may play a role in tissue development though interactions with members of the transforming growth factor beta family, such as bone morphogenetic proteins. [provided by RefSeq, Nov 2010]

Known Variants105 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs181698387	2:36,582,820	T/G	—	—
rs1668788483	2:36,583,442	T/G	—	uncertain significance
rs3821169	2:36,583,461	G/T	—	benign
rs759979001	2:36,583,472	T/C	—	uncertain significance
rs373748249	2:36,583,500	G/T	—	uncertain significance
rs534996132	2:36,583,511	C/A	—	benign
rs762557289	2:36,583,576	G/A	—	likely benign
rs201724622	2:36,583,725	A/G	—	uncertain significance
rs140753944	2:36,583,759	T/C	—	benign
rs781775912	2:36,583,763	G/C	—	uncertain significance
rs113549769	2:36,583,771	G/A	—	benign
rs17018667	2:36,613,369	G/A	intron variant	—
rs7604086	2:36,619,121	C/A	intron variant	—
rs17018688	2:36,619,609	C/A	—	—
rs1007958621	2:36,623,831	A/G	—	uncertain significance
rs774406061	2:36,623,862	G/A	—	uncertain significance
rs80144250	2:36,626,934	A/T	—	—
rs57785523	2:36,654,510	A/G	intron variant	—
rs1477048	2:36,660,476	G/C	regulatory region variant	—
rs17018786	2:36,662,533	G/C	intron variant	—
rs56036545	2:36,665,052	G/A	intron variant	—
rs370583153	2:36,668,393	C/T	—	likely benign
rs1675801553	2:36,668,427	C/T	—	uncertain significance
rs771686787	2:36,668,509	C/G	—	uncertain significance
rs147453426	2:36,668,573	C/T	—	likely benign
rs34360681	2:36,668,594	A/G	—	benign
rs574996264	2:36,668,608	C/T	—	uncertain significance
rs774686267	2:36,668,638	A/C	—	uncertain significance
rs140886695	2:36,669,781	G/A	—	uncertain significance
rs369675156	2:36,669,814	C/G	—	uncertain significance
rs140450317	2:36,669,816	C/G	—	benign
rs1675953445	2:36,669,870	G/T	—	uncertain significance
rs7562790	2:36,673,555	T/A	—	—
rs848512	2:36,675,530	A/C	—	—
rs888078	2:36,681,193	G/T	—	—
rs3755206	2:36,683,428	T/G	regulatory region variant	—
rs372989532	2:36,691,681	G/A	—	uncertain significance
rs1418937020	2:36,691,688	T/C	—	uncertain significance
rs1401059667	2:36,691,706	T/C	—	uncertain significance
rs373577546	2:36,691,711	G/A	—	uncertain significance
rs199612229	2:36,691,736	G/A	—	uncertain significance
rs752686443	2:36,704,083	T/C	—	uncertain significance
rs142409995	2:36,704,089	G/A	missense variant	—
rs150977654	2:36,704,095	A/G	—	uncertain significance
rs143230045	2:36,704,104	G/A	—	uncertain significance
rs145972275	2:36,704,117	C/T	—	benign
rs758619983	2:36,704,141	C/G	—	uncertain significance
rs188554284	2:36,706,671	C/G	—	benign
rs113372122	2:36,706,700	A/C	—	likely benign
rs572243696	2:36,706,702	G/C	—	uncertain significance
rs202222795	2:36,706,708	C/G	—	uncertain significance
rs759674160	2:36,706,709	G/A	—	uncertain significance
rs1316181002	2:36,706,744	G/A	—	likely benign
rs147700058	2:36,706,770	G/A	—	benign
rs77551206	2:36,706,773	C/G	—	likely benign
rs138940127	2:36,706,788	C/G	—	benign
rs141419153	2:36,706,801	G/T	—	uncertain significance
rs4670562	2:36,719,390	A/C	regulatory region variant	—
rs2465869985	2:36,726,388	C/T	—	uncertain significance
rs770825553	2:36,726,461	A/G	—	uncertain significance
rs773882030	2:36,726,469	C/T	—	uncertain significance
rs59890798	2:36,726,500	C/G	—	benign
rs2030645	2:36,733,328	A/T	—	—
rs12997487	2:36,737,128	A/G	—	benign
rs746819860	2:36,737,146	C/T	—	uncertain significance
rs776372225	2:36,737,154	A/C	—	uncertain significance
rs79366315	2:36,737,211	C/G	—	likely benign
rs147714435	2:36,737,222	G/A	—	uncertain significance
rs1572896455	2:36,737,272	C/T	—	likely benign
rs138250886	2:36,740,709	T/C	—	likely benign
rs748646981	2:36,740,728	C/A	—	uncertain significance
rs200415445	2:36,740,738	C/T	—	uncertain significance
rs574844817	2:36,740,749	G/A	—	likely benign
rs78900278	2:36,740,787	C/T	—	benign
rs757763520	2:36,744,520	G/A	—	uncertain significance
rs2466000549	2:36,744,563	T/C	—	uncertain significance
rs778622025	2:36,744,595	G/A	—	uncertain significance
rs749222285	2:36,744,629	C/T	—	uncertain significance
rs1665106431	2:36,744,652	C/T	—	uncertain significance
rs2466002413	2:36,744,679	T/A	—	uncertain significance
rs59929305	2:36,749,369	G/A	—	uncertain significance
rs914410630	2:36,749,454	T/G	—	uncertain significance
rs112092468	2:36,756,689	T/G	—	—
rs545095845	2:36,759,584	C/G	—	—
rs753244101	2:36,764,548	G/A	—	uncertain significance
rs2466164557	2:36,764,563	G/A	—	uncertain significance
rs113863774	2:36,764,607	C/A	—	likely benign
rs149188754	2:36,764,632	C/A	—	uncertain significance
rs201789171	2:36,764,633	C/T	—	uncertain significance
rs10084382	2:36,768,447	C/G	—	—
rs1316495060	2:36,771,546	T/C	—	uncertain significance
rs559985591	2:36,771,624	T/C	—	uncertain significance
rs116656609	2:36,771,625	C/T	—	benign
rs186746241	2:36,774,119	T/C	—	likely benign
rs1667395205	2:36,774,136	A/G	—	uncertain significance
rs1667401928	2:36,774,216	C/T	—	uncertain significance
rs1346777567	2:36,774,241	T/C	—	uncertain significance
rs142808862	2:36,774,247	C/T	—	uncertain significance
rs13419534	2:36,774,269	G/C	—	uncertain significance
rs755591519	2:36,774,309	A/G	—	likely benign

Showing 100 of 105 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.