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 FAM189A1 CNV Assays ›
Gene Symbol
FAM189A1
Assay Reference Genome
Location

Chr.15:29154678 on build GRCh38
Cytoband
15q13.1
Assay ID Hs05329314_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 23359

Gene Name:

 family with sequence similarity 189 member A1

Gene Aliases:

 TMEM228

Location:

 Chr.15:29120252-29570723 on Build GRCh38

Assay Gene Location:

 Within Intron 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM189A1 NM_015307.1 NP_056122.1
XM_011521407.2 XP_011519709.1
AB011146.1 BAA25500.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1040778 Chr.15:28689598 - 30515727 on Build GRCh38 Loss PDCD6IPP2 LOC101060569 LOC100289656 LOC107984752 APBA2 LOC105370751 ULK4P3 WHAMMP2 NSMCE3 GOLGA8T GOLGA6L7P CHRFAM7A LOC100130111 DKFZP434L187 GOLGA8M TJP1 FAM189A1 GOLGA8R LOC105370746 GOLGA8J
nsv527255 Chr.15:28754022 - 30074044 on Build GRCh38 Gain PDCD6IPP2 LOC100130111 LOC100289656 TJP1 LOC107984752 APBA2 FAM189A1 WHAMMP2 NSMCE3 GOLGA6L7P
esv2751526 Chr.15:28724519 - 30687025 on Build GRCh38 Loss LOC101927579 ULK4P2 ARHGAP11B LOC105370751 NSMCE3 GOLGA8T LOC100996413 LOC100130111 DKFZP434L187 LOC100288637 LOC105370746 PDCD6IPP2 LOC101060569 LOC100289656 LOC107984752 APBA2 ULK4P3 WHAMMP2 GOLGA6L7P CHRFAM7A GOLGA8H TJP1 FAM189A1 GOLGA8R GOLGA8J
nsv1039798 Chr.15:28724126 - 30158154 on Build GRCh38 Gain PDCD6IPP2 LOC100289656 LOC107984752 APBA2 ULK4P3 WHAMMP2 NSMCE3 GOLGA8T GOLGA6L7P LOC100130111 TJP1 FAM189A1 GOLGA8J
nsv568675 Chr.15:29035149 - 29916451 on Build GRCh38 Gain LOC100130111 TJP1 APBA2 FAM189A1 NSMCE3
nsv524362 Chr.15:29089598 - 29155854 on Build GRCh38 Loss APBA2 FAM189A1

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs80335077] 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 DGV Variation

Back To Top

Related Products