FLRT1

fibronectin leucine rich transmembrane protein 1

Summary

This gene encodes a member of the fibronectin leucine rich transmembrane protein (FLRT) family. The family members may function in cell adhesion and/or receptor signalling. Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix. The encoded protein shares sequence similarity with two other family members, FLRT2 and FLRT3. This gene is expressed in kidney and brain. [provided by RefSeq, Jul 2008]

Known Variants163 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs562664	11:63,823,619	C/T	intron variant	—
rs4980520	11:63,833,088	A/C	intron variant	—
rs117569191	11:63,851,888	G/A	intron variant	—
rs2701540	11:63,869,107	T/C	—	—
rs572740326	11:63,869,793	C/T	—	—
rs4980504	11:63,873,083	G/C	—	—
rs651359	11:63,876,201	T/G	—	—
rs57779243	11:63,882,363	G/T	downstream gene variant	—
rs2495610862	11:63,883,771	C/A	—	uncertain significance
rs200658385	11:63,883,775	C/T	—	likely benign
rs139768227	11:63,883,777	C/G	—	uncertain significance
rs547325012	11:63,883,796	G/A	—	benign
rs143337663	11:63,883,803	G/A	—	conflicting classifications of pathogenicity
rs199858445	11:63,883,825	T/A	—	uncertain significance
rs1042224142	11:63,883,833	C/A	—	likely benign
rs200588570	11:63,883,847	C/T	—	benign
rs774610946	11:63,883,853	C/G	—	uncertain significance
rs146061545	11:63,883,856	C/T	—	benign
rs958881632	11:63,883,862	C/T	—	likely benign
rs2495612005	11:63,883,894	C/G	—	uncertain significance
rs1944983108	11:63,883,915	G/A	—	uncertain significance
rs749956699	11:63,883,919	C/T	—	likely benign
rs779934784	11:63,883,925	C/T	—	likely benign
rs749232008	11:63,883,926	G/A	—	uncertain significance
rs777177875	11:63,883,950	G/C	—	uncertain significance
rs200049740	11:63,883,967	C/T	—	likely benign
rs770193280	11:63,883,968	G/A	—	uncertain significance
rs614397	11:63,883,985	C/T	—	benign
rs370410537	11:63,883,990	C/T	—	uncertain significance
rs201354922	11:63,884,024	C/T	—	likely benign
rs614035	11:63,884,027	C/T	—	benign
rs771072390	11:63,884,029	G/C	—	uncertain significance
rs772794847	11:63,884,081	C/T	—	likely benign
rs200610220	11:63,884,119	G/A	—	uncertain significance
rs201296024	11:63,884,128	G/A	—	uncertain significance
rs116999073	11:63,884,146	A/G	—	likely benign
rs756250929	11:63,884,176	C/T	—	uncertain significance
rs80061941	11:63,884,182	C/G	—	uncertain significance
rs774763930	11:63,884,184	C/T	—	uncertain significance
rs61731568	11:63,884,196	C/T	—	benign
rs1348763003	11:63,884,210	C/A	—	uncertain significance
rs767596236	11:63,884,234	C/T	—	likely benign
rs756090482	11:63,884,235	G/A	—	uncertain significance
rs141684580	11:63,884,252	C/T	—	likely benign
rs941880462	11:63,884,253	G/A	—	uncertain significance
rs148012979	11:63,884,262	G/A	—	uncertain significance
rs1386084347	11:63,884,281	T/G	—	uncertain significance
rs1266306392	11:63,884,320	C/T	—	uncertain significance
rs563036980	11:63,884,324	G/C	—	likely benign
rs1590932597	11:63,884,406	A/G	—	uncertain significance
rs565858250	11:63,884,415	C/T	—	uncertain significance
rs771760157	11:63,884,416	G/A	—	uncertain significance
rs754088054	11:63,884,438	G/A	—	likely benign
rs3751120	11:63,884,453	C/T	—	benign
rs377112197	11:63,884,459	C/T	—	likely benign
rs1565241569	11:63,884,461	A/T	—	uncertain significance
rs928607984	11:63,884,462	C/T	—	likely benign
rs3751121	11:63,884,474	C/T	—	benign
rs756527574	11:63,884,475	C/T	—	uncertain significance
rs146150625	11:63,884,501	G/A	—	likely benign
rs776773158	11:63,884,515	C/T	—	uncertain significance
rs377020952	11:63,884,516	G/A	—	likely benign
rs139711112	11:63,884,522	C/T	—	likely benign
rs145828331	11:63,884,525	G/A	—	benign
rs34856996	11:63,884,561	A/G	—	benign
rs2134620058	11:63,884,564	C/T	—	likely benign
rs757875522	11:63,884,605	C/T	—	uncertain significance
rs202201413	11:63,884,609	G/A	—	likely benign
rs770098892	11:63,884,620	G/T	—	uncertain significance
rs145399902	11:63,884,632	G/A	—	benign
rs185115330	11:63,884,654	C/A	—	uncertain significance
rs757865702	11:63,884,672	C/T	—	likely benign
rs777150139	11:63,884,673	G/A	—	uncertain significance
rs151215662	11:63,884,684	C/T	—	likely benign
rs140370010	11:63,884,690	G/A	—	likely benign
rs149882049	11:63,884,716	G/A	—	uncertain significance
rs772744996	11:63,884,735	T/C	—	likely benign
rs35247680	11:63,884,747	T/C	—	benign
rs762577383	11:63,884,760	G/C	—	uncertain significance
rs763641756	11:63,884,766	G/C	—	uncertain significance
rs751115779	11:63,884,768	G/A	—	likely benign
rs202104543	11:63,884,779	C/T	—	uncertain significance
rs1945005930	11:63,884,781	G/A	—	uncertain significance
rs779105954	11:63,884,784	G/A	—	uncertain significance
rs1590933528	11:63,884,805	A/C	—	uncertain significance
rs767022154	11:63,884,830	G/A	—	uncertain significance
rs570176314	11:63,884,858	C/A	—	uncertain significance
rs138445479	11:63,884,859	G/C	—	uncertain significance
rs748392464	11:63,884,861	G/C	—	likely benign
rs773930935	11:63,884,881	C/G	—	uncertain significance
rs141342857	11:63,884,894	C/T	—	likely benign
rs143408791	11:63,884,897	C/T	—	likely benign
rs1160952835	11:63,884,907	G/A	—	uncertain significance
rs148382868	11:63,884,909	G/T	—	benign
rs138676741	11:63,884,923	C/T	—	likely benign
rs374535379	11:63,884,941	C/A	—	uncertain significance
rs369112014	11:63,884,950	C/T	—	uncertain significance
rs764179577	11:63,884,951	G/A	—	likely benign
rs914896380	11:63,884,968	T/A	—	uncertain significance
rs769032516	11:63,884,992	G/A	—	uncertain significance

Showing 100 of 163 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.