accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other DST CNV Assays ›
Gene Symbol
DST
Assay Reference Genome
Location

Chr.6:56860766 on build GRCh38
Cytoband
6p12.1
Assay ID Hs06787010_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 667

Gene Name:

 dystonin

Gene Aliases:

 BP240, BPA, BPAG1, CATX-15, CATX15, D6S1101, DMH, DT, EBSB2, HSAN6, MACF2

Location:

 Chr.6:56457987-56954671 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
DST NM_001144769.2 NP_001138241.1
XM_005249310.3 XP_005249367.1
XM_005249315.3 XP_005249372.1
XM_011514824.2 XP_011513126.1
XM_011514825.2 XP_011513127.1
XM_017011205.1 XP_016866694.1
XM_017011206.1 XP_016866695.1
XM_017011207.1 XP_016866696.1
XM_017011208.1 XP_016866697.1
XM_017011209.1 XP_016866698.1
XM_017011210.1 XP_016866699.1
XM_017011211.1 XP_016866700.1
XM_017011212.1 XP_016866701.1
XM_017011213.1 XP_016866702.1
XM_017011214.1 XP_016866703.1
XM_017011215.1 XP_016866704.1
XM_017011216.1 XP_016866705.1
XM_017011219.1 XP_016866708.1
XM_017011220.1 XP_016866709.1
XM_017011221.1 XP_016866710.1
XM_017011223.1 XP_016866712.1
XM_017011225.1 XP_016866714.1
DN994324.1
U31851.1 AAC50244.1

Target Gene Details

Entrez Gene ID:

 101930010

Gene Name:

 uncharacterized LOC101930010

Gene Aliases:

 -

Location:

 Chr.6:56843986-56864338 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC101930010 NR_125866.1
CK819990.1

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs112516699] 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

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products