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See other MGC32805 CNV Assays ›
Gene Symbol
MGC32805
Assay Reference Genome
Location

Chr.5:122458211 on build GRCh38
Cytoband
5q23.2
Assay ID Hs06037053_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 153163

Gene Name:

 uncharacterized LOC153163

Gene Aliases:

 -

Location:

 Chr.5:122436497-122479087 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MGC32805 NR_051996.1

Target Gene Details

Entrez Gene ID:

 9627

Gene Name:

 synuclein alpha interacting protein

Gene Aliases:

 SYPH1, Sph1

Location:

 Chr.5:122311354-122464219 on Build GRCh38

Assay Gene Location:

 Within Intron 21
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SNCAIP NM_001242935.2 NP_001229864.1
NM_001308100.1 NP_001295029.1
NM_001308105.1 NP_001295034.1
NM_001308106.1 NP_001295035.1
NM_001308107.1 NP_001295036.1
NM_001308108.1 NP_001295037.1
NM_001308109.1 NP_001295038.1
NM_005460.3 NP_005451.2
NR_131761.1
NR_131762.1
XM_005272138.3 XP_005272195.1
XM_005272139.1 XP_005272196.1
XM_006714734.2 XP_006714797.1
XM_011543737.2 XP_011542039.1
XM_011543738.2 XP_011542040.1
XM_011543739.1 XP_011542041.1
XM_011543741.2 XP_011542043.1
XM_011543743.2 XP_011542045.1
XM_011543745.1 XP_011542047.1
XM_011543749.2 XP_011542051.1
XM_011543750.1 XP_011542052.1
XM_017010078.1 XP_016865567.1
XM_017010081.1 XP_016865570.1
XM_017010082.1 XP_016865571.1
XM_017010083.1 XP_016865572.1
XM_017010085.1 XP_016865574.1
AF076929.1 AAD30362.1
AK001617.1 BAA91791.1
AK021944.1
AK299687.1
AK304646.1
BC033743.1
BC040552.1 AAH40552.1
BC094759.1 AAH94759.1
DQ227317.1 ABB51162.1

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More Information


Additional Information:

For this assay, SNP(s) [rs372340125] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Intronic Non-exonic non-DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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