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See other FAM189A1 CNV Assays ›
Gene Symbol
FAM189A1
Assay Reference Genome
Location

Chr.15:29130904 on build GRCh38
Cytoband
15q13.1
Assay ID Hs05346910_cn
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Availability Made To Order
Catalog # 4400291
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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 8
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 GOLGA8R GOLGA8J CHRFAM7A LOC105370751 DKFZP434L187 LOC100130111 APBA2 NSMCE3 WHAMMP2 TJP1 LOC101060569 LOC105370746 LOC107984752 GOLGA8M PDCD6IPP2 ULK4P3 LOC100289656 GOLGA6L7P GOLGA8T FAM189A1
nsv515798 Chr.15:29068198 - 29146274 on Build GRCh38 Gain+Loss APBA2 FAM189A1
nsv471232 Chr.15:29087561 - 29139979 on Build GRCh38 Loss APBA2 FAM189A1
nsv527255 Chr.15:28754022 - 30074044 on Build GRCh38 Gain TJP1 LOC100130111 LOC107984752 APBA2 NSMCE3 PDCD6IPP2 WHAMMP2 LOC100289656 GOLGA6L7P FAM189A1
esv2751526 Chr.15:28724519 - 30687025 on Build GRCh38 Loss APBA2 NSMCE3 LOC100288637 ARHGAP11B LOC101060569 LOC105370746 GOLGA6L7P FAM189A1 GOLGA8R GOLGA8J CHRFAM7A LOC105370751 DKFZP434L187 LOC100130111 LOC100996413 WHAMMP2 GOLGA8H TJP1 LOC107984752 ULK4P2 PDCD6IPP2 ULK4P3 LOC100289656 LOC101927579 GOLGA8T
nsv1039798 Chr.15:28724126 - 30158154 on Build GRCh38 Gain GOLGA8J LOC100130111 APBA2 NSMCE3 WHAMMP2 TJP1 LOC107984752 PDCD6IPP2 ULK4P3 LOC100289656 GOLGA6L7P GOLGA8T FAM189A1
nsv568675 Chr.15:29035149 - 29916451 on Build GRCh38 Gain TJP1 LOC100130111 APBA2 NSMCE3 FAM189A1
nsv524362 Chr.15:29089598 - 29155854 on Build GRCh38 Loss APBA2 FAM189A1

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More Information


Additional Information:

For this assay, SNP(s) [rs74009303] 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

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