CD164

CD164 molecule

Summary

This gene encodes a transmembrane sialomucin and cell adhesion molecule that regulates the proliferation, adhesion and migration of hematopoietic progenitor cells. The encoded protein also interacts with the C-X-C chemokine receptor type 4 and may regulate muscle development. Elevated expression of this gene has been observed in human patients with Sezary syndrome, a type of blood cancer, and a mutation in this gene may be associated with impaired hearing. [provided by RefSeq, Oct 2016]

Known Variants93 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs974034	6:109,689,431	A/G	—	benign
rs147143577	6:109,689,521	T/A	—	likely benign
rs9487074	6:109,689,681	T/C	—	benign
rs554606303	6:109,689,734	G/C	—	likely benign
rs9487075	6:109,689,902	C/T	—	benign
rs11251	6:109,689,907	G/T	—	benign
rs757645536	6:109,690,057	C/T	—	likely benign
rs62436104	6:109,690,073	C/T	—	likely benign
rs876661402	6:109,690,074	G/A	stop gained	no classifications from unflagged records
rs1166070682	6:109,690,077	C/T	—	uncertain significance
rs780424542	6:109,690,085	T/C	—	uncertain significance
rs746589702	6:109,690,091	A/T	—	uncertain significance
rs375553590	6:109,690,099	A/C	—	likely benign
rs147393458	6:109,690,100	A/G	—	uncertain significance
rs773099923	6:109,690,107	A/G	—	uncertain significance
rs752047597	6:109,690,198	A/C	—	likely benign
rs368514410	6:109,690,232	G/C	—	benign
rs117030454	6:109,690,517	A/G	—	likely benign
rs2275649	6:109,691,328	T/C	—	benign
rs371819591	6:109,691,598	A/G	—	likely benign
rs562238936	6:109,691,621	A/C	—	likely benign
rs145269975	6:109,691,627	T/C	—	likely benign
rs748276344	6:109,691,632	T/G	—	uncertain significance
rs2115144052	6:109,691,637	G/T	—	uncertain significance
rs9480941	6:109,691,639	T/C	—	benign
rs148700319	6:109,691,641	T/C	—	uncertain significance
rs766602425	6:109,691,644	A/G	—	uncertain significance
rs767974518	6:109,691,663	G/A	—	benign
rs369526532	6:109,691,688	T/G	—	likely benign
rs115099723	6:109,691,766	T/C	—	benign
rs3818933	6:109,691,944	G/A	—	benign
rs9487076	6:109,692,727	T/C	intron variant	—
rs11753645	6:109,695,054	T/C	regulatory region variant	—
rs34131679	6:109,697,051	C/A	—	benign
rs145666240	6:109,697,083	T/C	—	likely benign
rs771601649	6:109,697,285	T/C	—	uncertain significance
rs373906087	6:109,697,308	C/T	—	likely benign
rs1265838441	6:109,697,319	T/C	—	uncertain significance
rs117668371	6:109,697,599	A/C	—	benign
rs114995468	6:109,699,045	C/G	—	likely benign
rs377505131	6:109,699,092	T/G	—	likely benign
rs142043630	6:109,699,103	C/T	—	uncertain significance
rs199887608	6:109,699,104	G/A	—	conflicting classifications of pathogenicity
rs752639259	6:109,699,131	T/A	—	uncertain significance
rs1451115611	6:109,699,152	G/A	—	likely benign
rs556025572	6:109,699,158	T/C	—	likely benign
rs1048861219	6:109,699,159	G/A	—	uncertain significance
rs376261079	6:109,699,171	T/C	—	uncertain significance
rs757764538	6:109,699,182	G/A	—	likely benign
rs1562242001	6:109,699,185	G/A	—	likely benign
rs1407620	6:109,699,359	C/T	—	benign
rs35452836	6:109,699,446	A/T	—	benign
rs77504265	6:109,700,632	C/A	—	benign
rs142190227	6:109,700,762	G/C	—	benign
rs2482455020	6:109,700,764	A/C	—	likely benign
rs2482455056	6:109,700,770	A/C	—	likely benign
rs201168621	6:109,700,808	G/A	—	uncertain significance
rs762977439	6:109,700,820	C/T	—	likely benign
rs1270280249	6:109,700,832	C/T	—	likely benign
rs145357332	6:109,700,847	T/C	—	likely benign
rs191386841	6:109,700,851	G/C	—	likely benign
rs377262294	6:109,700,856	T/C	—	uncertain significance
rs139218322	6:109,700,873	G/A	—	likely benign
rs551697941	6:109,700,877	G/A	—	likely benign
rs775223140	6:109,700,881	G/C	—	likely benign
rs2275651	6:109,701,056	T/G	—	benign
rs1486349483	6:109,702,718	G/C	—	likely benign
rs548129524	6:109,702,767	T/A	—	benign
rs73762715	6:109,702,776	G/A	—	benign
rs532750274	6:109,703,170	C/G	—	benign
rs11963133	6:109,703,241	G/C	—	benign
rs77498953	6:109,703,307	C/T	—	benign
rs4313033	6:109,703,327	G/A	—	likely benign
rs1885691	6:109,703,391	C/T	—	benign
rs1192435598	6:109,703,414	C/G	—	likely benign
rs2482473942	6:109,703,419	T/A	—	likely benign
rs113902228	6:109,703,451	G/A	—	likely benign
rs747990184	6:109,703,459	G/A	—	likely benign
rs2115177023	6:109,703,469	G/A	—	uncertain significance
rs2482474697	6:109,703,470	G/C	—	uncertain significance
rs750780867	6:109,703,494	G/A	—	uncertain significance
rs138925698	6:109,703,524	C/A	—	uncertain significance
rs775630795	6:109,703,545	T/C	—	likely benign
rs761993548	6:109,703,557	G/A	—	uncertain significance
rs373195063	6:109,703,567	G/A	—	likely benign
rs376141842	6:109,703,584	T/C	—	likely benign
rs1490904351	6:109,703,593	C/T	—	uncertain significance
rs190842782	6:109,703,622	G/C	—	benign
rs2275652	6:109,703,683	G/C	—	benign
rs1322816	6:109,703,727	C/A	—	benign
rs115225098	6:109,703,868	A/T	—	likely benign
rs1322815	6:109,704,062	A/G	—	benign
rs115705232	6:109,704,091	G/A	—	benign

Gene information from NCBI Gene. Variant classifications from ClinVar.