MUC19

mucin 19, oligomeric (gene/pseudogene)

Summary

This gene encodes a member of the gel-forming mucin protein family. Mucin family members are glycoproteins that have tandem repeats which are extensively O-glycosylated. The structural features of mucin proteins are responsible for the gel-like properties of mucus. The encoded protein may be involved in disruption of the ocular surface in Sjogren syndrome. [provided by RefSeq, Apr 2014]

Known Variants41 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs11564258	12:40,792,300	G/A	intron variant	—
rs367804593	12:40,799,851	C/T	—	likely benign
rs143082493	12:40,802,161	A/G	—	likely benign
rs377640287	12:40,810,145	T/A	—	likely benign
rs369743721	12:40,810,148	A/G	—	likely benign
rs897536763	12:40,811,945	G/A	—	likely benign
rs11564245	12:40,823,354	G/C	missense variant	—
rs144344916	12:40,825,459	G/A	—	likely benign
rs767138360	12:40,830,496	G/A	—	likely benign
rs4768261	12:40,834,918	C/A	missense variant	—
rs151020006	12:40,834,946	C/T	—	likely benign
rs201032823	12:40,838,217	G/A	—	likely benign
rs777356323	12:40,844,490	G/A	—	likely benign
rs2933353	12:40,857,943	A/C	missense variant	—
rs531019133	12:40,859,390	T/C	—	likely benign
rs55755644	12:40,873,252	G/A	—	likely benign
rs149170137	12:40,874,383	C/T	—	likely benign
rs191798371	12:40,875,829	G/A	—	likely benign
rs1948589424	12:40,878,694	A/T	—	likely benign
rs144308011	12:40,879,532	G/A	—	likely benign
rs2498357522	12:40,879,548	C/T	—	likely benign
rs567412382	12:40,879,601	A/T	—	likely benign
rs542552030	12:40,880,153	T/G	—	likely benign
rs990443397	12:40,880,315	G/T	—	likely benign
rs939404951	12:40,880,384	A/G	—	likely benign
rs1191575185	12:40,883,177	A/G	—	likely benign
rs2498366710	12:40,883,702	A/T	—	likely benign
rs79690920	12:40,884,212	A/T	—	likely benign
rs1948651870	12:40,884,305	G/C	—	likely benign
rs368749839	12:40,884,986	A/C	—	likely benign
rs182469326	12:40,894,983	C/A	—	likely benign
rs559539642	12:40,895,001	C/A	—	likely benign
rs546346683	12:40,900,088	C/T	—	likely benign
rs536871012	12:40,900,806	C/T	—	likely benign
rs1939001558	12:40,904,807	C/A	—	likely benign
rs973493842	12:40,908,980	C/A	—	likely benign
rs201184443	12:40,924,241	C/G	intron variant	—
rs61730699	12:40,931,474	G/A	—	likely benign
rs376066372	12:40,935,636	A/G	—	likely benign
rs1170775175	12:40,936,598	G/A	—	likely benign
rs1351613880	12:40,954,807	C/T	—	likely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.