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See other LOC100128568 CNV Assays ›
Gene Symbol
LOC100128568
Assay Reference Genome
Location

Chr.19:5994179 on build GRCh38
Cytoband
19p13.3
Assay ID Hs00844064_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 100128568

Gene Name:

 uncharacterized LOC100128568

Gene Aliases:

 -

Location:

 Chr.19:5978403-6020363 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC100128568 NR_046376.1

Target Gene Details

Entrez Gene ID:

 5990

Gene Name:

 regulatory factor X2

Gene Aliases:

 -

Location:

 Chr.19:5993164-6110653 on Build GRCh38

Assay Gene Location:

 Within Exon 19
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RFX2 NM_000635.3 18 3097 NP_000626.2
NM_134433.2 17 3022 NP_602309.1
XM_011528171.2 19 3063 XP_011526473.1
XM_011528172.1 18 2924 XP_011526474.1
XM_017027107.1 17 2947 XP_016882596.1
XM_017027108.1 16 2872 XP_016882597.1
AK024288.1 15 2636
BC028579.1 18 3009 AAH28579.1
BC071571.1 18 2978 AAH71571.1
BX648130.1 18 2932

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3583213 Chr.19:5989712 - 6000302 on Build GRCh38 Loss LOC100128568 RFX2

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More Information


Additional Information:

For this assay, SNP(s) [rs148370194] 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 Exonic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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