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

Chr.15:29121364 on build GRCh38
Cytoband
15q13.1
Assay ID Hs03893193_cn
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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 Exon 12
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM189A1 NM_015307.1 11 3595 NP_056122.1
XM_011521407.2 12 3752 XP_011519709.1
AB011146.1 8 3195 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 WHAMMP2 APBA2 GOLGA6L7P FAM189A1 LOC100289656 LOC100130111 TJP1 ULK4P3 DKFZP434L187 GOLGA8M GOLGA8J LOC101060569 GOLGA8T LOC107984752 LOC105370751 PDCD6IPP2 LOC105370746 GOLGA8R CHRFAM7A NSMCE3
nsv9228 Chr.15:29118128 - 29122991 on Build GRCh38 Loss APBA2 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 WHAMMP2 APBA2 LOC107984752 PDCD6IPP2 GOLGA6L7P FAM189A1 LOC100289656 NSMCE3 LOC100130111 TJP1
esv2751526 Chr.15:28724519 - 30687025 on Build GRCh38 Loss WHAMMP2 GOLGA6L7P FAM189A1 GOLGA8J GOLGA8T LOC107984752 PDCD6IPP2 LOC105370746 LOC100288637 GOLGA8R LOC101927579 LOC100996413 APBA2 LOC100289656 ULK4P2 LOC100130111 GOLGA8H ARHGAP11B TJP1 ULK4P3 DKFZP434L187 LOC101060569 LOC105370751 CHRFAM7A NSMCE3
nsv1039798 Chr.15:28724126 - 30158154 on Build GRCh38 Gain WHAMMP2 APBA2 GOLGA6L7P FAM189A1 LOC100289656 LOC100130111 TJP1 ULK4P3 GOLGA8J GOLGA8T LOC107984752 PDCD6IPP2 NSMCE3
nsv568679 Chr.15:29119123 - 29126370 on Build GRCh38 Loss FAM189A1
nsv568675 Chr.15:29035149 - 29916451 on Build GRCh38 Gain APBA2 FAM189A1 NSMCE3 LOC100130111 TJP1
nsv524362 Chr.15:29089598 - 29155854 on Build GRCh38 Loss APBA2 FAM189A1

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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