TENM3

teneurin transmembrane protein 3

Summary

This gene encodes a member of the teneurin transmembrane protein family. The encoded protein may be involved in the regulation of neuronal development including development of the visual pathway. Mutations in this gene have been associated with microphthalmia and developmental dysplasia of the hip. [provided by RefSeq, Jan 2023]

Known Variants394 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs7672826	4:182,399,695	G/A	intergenic variant	—
rs573242904	4:182,451,692	C/A	—	—
rs1439283	4:182,484,769	C/T	intergenic variant	—
rs6815916	4:182,553,043	A/G	intergenic variant	—
rs12641856	4:182,609,865	G/A	regulatory region variant	—
rs530371276	4:182,657,399	C/T	—	—
rs6855088	4:182,704,551	A/T	—	—
rs192647746	4:182,760,366	A/G	upstream gene variant	—
rs10520514	4:182,782,545	T/A	intergenic variant	—
rs183898380	4:182,887,489	A/G	regulatory region variant	—
rs576189584	4:183,006,610	C/T	—	—
rs2726807	4:183,137,398	T/A	—	—
rs2726818	4:183,147,436	G/A	intron variant	—
rs62354179	4:183,149,741	C/T	—	—
rs11724903	4:183,200,145	A/G	intron variant	—
rs6828445	4:183,244,869	T/C	—	benign
rs77256039	4:183,244,927	G/A	—	benign
rs200908350	4:183,245,185	A/G	—	likely benign
rs145196616	4:183,245,209	G/A	—	likely benign
rs534555806	4:183,245,263	T/G	—	uncertain significance
rs2547197801	4:183,245,291	T/A	—	uncertain significance
rs2547198351	4:183,245,378	A/G	—	uncertain significance
rs571190774	4:183,248,178	G/A	—	—
rs10520528	4:183,260,601	T/G	regulatory region variant	—
rs6841633	4:183,267,490	T/A	—	benign
rs748767039	4:183,267,818	C/G	—	uncertain significance
rs745497530	4:183,267,833	G/A	—	uncertain significance
rs184709394	4:183,267,863	G/T	—	likely benign
rs189642302	4:183,267,874	G/T	—	benign
rs144353515	4:183,267,886	C/T	—	benign
rs368445725	4:183,267,965	A/G	—	uncertain significance
rs759894262	4:183,267,973	T/C	—	likely benign
rs761052824	4:183,267,985	G/T	—	likely benign
rs151089580	4:183,268,010	C/T	—	benign
rs1006918380	4:183,268,011	T/A	—	uncertain significance
rs760777000	4:183,268,101	T/C	—	likely benign
rs6552554	4:183,268,174	C/T	—	benign
rs4862046	4:183,300,614	A/G	intron variant	—
rs7692207	4:183,366,362	C/T	intron variant	—
rs533972607	4:183,463,118	A/C	—	—
rs10013166	4:183,477,329	G/A	regulatory region variant	—
rs6833629	4:183,521,798	G/A	—	benign
rs2152412167	4:183,522,089	G/A	—	likely benign
rs190272851	4:183,522,108	C/G	—	likely benign
rs2533068222	4:183,522,148	C/G	—	uncertain significance
rs946691972	4:183,522,176	A/G	—	uncertain significance
rs544813385	4:183,522,183	C/G	—	uncertain significance
rs17073618	4:183,522,186	C/T	—	benign
rs923678656	4:183,522,196	A/G	—	uncertain significance
rs370003429	4:183,522,200	G/A	—	uncertain significance
rs751685257	4:183,522,221	C/T	—	uncertain significance
rs781215278	4:183,522,234	C/T	—	likely benign
rs917596979	4:183,522,235	G/A	—	uncertain significance
rs77704253	4:183,522,449	A/G	—	benign
rs190672201	4:183,522,469	T/C	—	benign
rs28403363	4:183,522,526	A/G	—	benign
rs1748381052	4:183,527,150	T/G	—	uncertain significance
rs55903810	4:183,531,476	C/T	intron variant	—
rs2533518789	4:183,549,821	C/T	—	uncertain significance
rs74199039	4:183,549,831	T/G	—	benign
rs2533519544	4:183,549,851	C/G	—	uncertain significance
rs2533521554	4:183,549,972	C/A	—	uncertain significance
rs1751080113	4:183,549,994	G/A	—	uncertain significance
rs1457472687	4:183,550,007	C/T	—	uncertain significance
rs557307443	4:183,550,008	G/A	—	benign
rs143539987	4:183,550,245	A/G	—	likely benign
rs114431061	4:183,574,794	A/G	—	benign
rs17073713	4:183,574,838	A/G	—	benign
rs1297325266	4:183,574,918	C/G	—	uncertain significance
rs374694049	4:183,574,985	T/C	—	likely benign
rs1753535990	4:183,575,016	A/C	—	uncertain significance
rs368777500	4:183,575,053	G/A	—	likely benign
rs17073715	4:183,575,356	C/T	—	benign
rs3749508	4:183,594,117	A/T	—	benign
rs761249047	4:183,594,176	C/T	—	uncertain significance
rs192736990	4:183,594,243	T/C	—	likely benign
rs201144002	4:183,594,275	T/C	—	uncertain significance
rs566460672	4:183,594,278	A/G	—	uncertain significance
rs1422652087	4:183,594,287	A/G	—	uncertain significance
rs1040552339	4:183,594,292	C/G	—	uncertain significance
rs376960815	4:183,594,304	A/C	—	uncertain significance
rs201935622	4:183,594,352	T/A	—	uncertain significance
rs201014580	4:183,594,357	G/A	—	benign
rs745896405	4:183,594,376	A/C	—	uncertain significance
rs755138158	4:183,600,828	G/A	—	uncertain significance
rs200278921	4:183,600,871	G/A	—	uncertain significance
rs200203346	4:183,600,886	C/T	—	uncertain significance
rs200560090	4:183,600,897	G/A	—	conflicting classifications of pathogenicity
rs190762721	4:183,600,901	G/A	—	uncertain significance
rs375578627	4:183,600,908	G/A	—	likely benign
rs774002460	4:183,600,918	A/G	—	uncertain significance
rs377048617	4:183,600,919	G/A	—	uncertain significance
rs563892336	4:183,600,921	C/T	—	uncertain significance
rs202194507	4:183,600,933	G/A	—	conflicting classifications of pathogenicity
rs776432015	4:183,600,934	G/A	—	uncertain significance
rs761664403	4:183,600,941	C/G	—	uncertain significance
rs533464172	4:183,601,005	G/T	—	uncertain significance
rs762266049	4:183,601,020	A/G	—	uncertain significance
rs78532078	4:183,601,134	A/C	—	benign
rs919662130	4:183,601,421	C/T	—	pathogenic

Showing 100 of 394 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.