MAP2

microtubule associated protein 2

Summary

This gene encodes a protein that belongs to the microtubule-associated protein family. The proteins of this family are thought to be involved in microtubule assembly, which is an essential step in neurogenesis. The products of similar genes in rat and mouse are neuron-specific cytoskeletal proteins that are enriched in dentrites, implicating a role in determining and stabilizing dentritic shape during neuron development. A number of alternatively spliced variants encoding distinct isoforms have been described. [provided by RefSeq, Jan 2010]

Known Variants117 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs13032935	2:210,297,576	T/C	intron variant	—
rs13012322	2:210,297,938	A/G	intron variant	—
rs62213410	2:210,300,731	A/G	—	—
rs4474826	2:210,318,264	A/G	intron variant	—
rs190457931	2:210,397,901	G/A	intron variant	—
rs149399489	2:210,414,655	G/A	regulatory region variant	—
rs140729377	2:210,479,987	C/T	regulatory region variant	—
rs9288410	2:210,498,261	G/C	—	—
rs145006403	2:210,516,482	G/T	intron variant	—
rs185429841	2:210,516,703	C/G	intron variant	—
rs138782038	2:210,517,907	C/T	—	uncertain significance
rs1559488151	2:210,517,918	A/G	—	likely benign
rs145598155	2:210,517,947	C/T	—	uncertain significance
rs754431951	2:210,517,948	G/A	—	likely benign
rs149857613	2:210,517,999	C/T	—	likely benign
rs148825736	2:210,518,011	A/G	—	likely benign
rs1231157687	2:210,518,022	G/A	—	uncertain significance
rs139310749	2:210,518,057	A/G	—	likely benign
rs2663647	2:210,521,705	T/A	intron variant	—
rs777568215	2:210,543,397	G/C	—	uncertain significance
rs375849922	2:210,557,420	G/A	—	benign
rs6749066	2:210,557,430	A/G	—	benign
rs1366274732	2:210,557,505	C/A	—	uncertain significance
rs763131046	2:210,557,628	T/G	—	uncertain significance
rs756595082	2:210,557,633	G/A	—	uncertain significance
rs547929820	2:210,557,706	C/T	—	likely benign
rs2468976703	2:210,557,745	T/C	—	uncertain significance
rs1477486506	2:210,557,769	T/G	—	uncertain significance
rs761272143	2:210,557,825	T/C	—	uncertain significance
rs554559632	2:210,557,982	A/G	—	uncertain significance
rs746572323	2:210,557,986	T/G	—	uncertain significance
rs776106329	2:210,557,996	A/G	—	likely benign
rs140194857	2:210,558,031	G/A	—	uncertain significance
rs767661117	2:210,558,069	A/G	—	uncertain significance
rs755708	2:210,558,113	G/T	—	benign
rs41265969	2:210,558,134	G/T	—	likely benign
rs2469000697	2:210,558,171	T/C	—	likely benign
rs2059460374	2:210,558,210	A/C	—	uncertain significance
rs2059464169	2:210,558,222	A/G	—	uncertain significance
rs2059484160	2:210,558,295	T/A	—	uncertain significance
rs141459532	2:210,558,299	G/A	—	likely benign
rs200834782	2:210,558,395	G/A	—	uncertain significance
rs1453398772	2:210,558,495	A/G	—	uncertain significance
rs757577771	2:210,558,789	C/T	—	uncertain significance
rs762406263	2:210,558,894	A/G	—	uncertain significance
rs35994200	2:210,558,931	T/C	—	benign
rs748316679	2:210,558,959	C/G	—	uncertain significance
rs148922251	2:210,559,050	G/A	—	likely benign
rs201346969	2:210,559,082	G/A	—	uncertain significance
rs142338628	2:210,559,148	G/T	—	uncertain significance
rs34693874	2:210,559,174	T/C	—	benign
rs184529696	2:210,559,239	C/T	—	benign
rs1281334154	2:210,559,351	G/A	—	likely benign
rs2469065701	2:210,559,355	T/G	—	uncertain significance
rs142716142	2:210,559,357	T/C	—	likely benign
rs150391168	2:210,559,417	G/A	—	benign
rs760878375	2:210,559,476	A/G	—	uncertain significance
rs757146059	2:210,559,491	A/T	—	uncertain significance
rs2469076238	2:210,559,523	G/A	—	uncertain significance
rs545513549	2:210,559,586	G/A	—	uncertain significance
rs749921089	2:210,559,610	A/G	—	uncertain significance
rs2469083249	2:210,559,658	G/A	—	uncertain significance
rs775061918	2:210,559,743	T/C	—	uncertain significance
rs377222605	2:210,559,793	A/G	—	uncertain significance
rs13425372	2:210,559,821	A/T	—	benign
rs1182655484	2:210,559,875	T/A	—	uncertain significance
rs777692339	2:210,559,881	A/G	—	uncertain significance
rs2469100460	2:210,559,940	G/A	—	uncertain significance
rs149636178	2:210,559,952	A/G	—	uncertain significance
rs756947989	2:210,560,000	C/G	—	uncertain significance
rs781042374	2:210,560,002	A/G	—	likely benign
rs1407795840	2:210,560,078	A/G	—	likely benign
rs758709004	2:210,560,082	A/G	—	uncertain significance
rs780833599	2:210,560,098	A/G	—	likely benign
rs199753872	2:210,560,114	G/A	—	uncertain significance
rs2469113315	2:210,560,161	T/A	—	uncertain significance
rs1296295852	2:210,560,166	T/A	—	uncertain significance
rs2469116498	2:210,560,211	G/A	—	uncertain significance
rs36091461	2:210,560,281	G/A	—	benign
rs746360359	2:210,560,318	A/G	—	uncertain significance
rs200843201	2:210,560,355	C/T	—	uncertain significance
rs1289033026	2:210,560,356	A/G	—	likely benign
rs376049781	2:210,560,392	C/T	—	likely benign
rs202122082	2:210,560,475	T/C	—	uncertain significance
rs565324625	2:210,560,520	A/G	—	uncertain significance
rs1392337437	2:210,560,569	C/G	—	uncertain significance
rs367929783	2:210,560,618	C/A	—	uncertain significance
rs142649637	2:210,560,646	G/A	—	uncertain significance
rs753201638	2:210,560,658	T/C	—	uncertain significance
rs758965405	2:210,560,672	C/A	—	uncertain significance
rs2060075745	2:210,560,693	G/C	—	uncertain significance
rs1236024310	2:210,560,715	C/A	—	uncertain significance
rs150116230	2:210,560,729	G/C	—	uncertain significance
rs746074088	2:210,560,826	T/G	—	uncertain significance
rs1196139416	2:210,560,873	G/C	—	uncertain significance
rs2469154153	2:210,560,916	C/T	—	uncertain significance
rs35915945	2:210,560,925	A/C	—	likely benign
rs780373367	2:210,560,960	A/G	—	uncertain significance
rs767960991	2:210,560,970	T/C	—	uncertain significance
rs935600713	2:210,561,071	C/A	—	uncertain significance

Showing 100 of 117 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.