Assay Details
Target Gene Details
Entrez Gene ID: | 28 |
Gene Name: | ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) |
Gene Aliases: |
A3GALNT, A3GALT1, GTB, NAGAT |
Location: |
Chr.9:133255176-133275214 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ABO | NM_020469.2 | NP_065202.2 | ||
AF134412.1 | AAD26572.1 | |||
AF134413.1 | AAD26573.1 | |||
AF134414.1 | AAD26574.1 | |||
AF134415.1 | ||||
AF134416.1 | ||||
AK302203.1 | ||||
AV761252.1 | ||||
BC069595.1 | AAH69595.1 | |||
BC069814.1 | AAH69814.1 | |||
BC111575.1 | ||||
DQ139865.1 | ||||
FR691751.1 | ||||
FR691752.1 | ||||
J05175.1 | AAA36792.1 | |||
JN791441.1 | ||||
JX398330.1 | ||||
JX398331.1 | ||||
JX398332.1 | ||||
JX398333.1 | ||||
JX519569.1 | ||||
JX519570.1 | ||||
KT282967.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2739138 | Chr.9:132727483 - 135521553 on Build GRCh38 | Deletion | PPP1R26-AS1 AK8 SNORD141A SURF1 MIR3689C REXO4 OLFM1 MIR548AW SARDH PPP1R26 LOC101448202 LOC101928525 TSC1 DBH LOC105376306 COL5A1-AS1 LOC100130548 GBGT1 ADAMTSL2 SNORD24 VAV2 SURF4 LOC100996574 SPACA9 RXRA ABO FAM163B LOC101928193 RPL7A OBP2B MIR6877 FCN2 CEL MIR3689A LOC401557 RALGDS GTF3C5 BRD3 MIR3689F DBH-AS1 COL5A1 MIR3689B LINC00094 MIR3689D1 SLC2A6 SURF2 ADAMTS13 GFI1B LCN1 MIR3689E SNORD36B FCN1 WDR5 TMEM8C MRPS2 MED22 C9orf62 MIR4669 SURF6 MIR3689D2 STKLD1 SNORD36A SNORD36C CACFD1 RNU6ATAC C9orf116 CELP |
nsv469905 | Chr.9:133174393 - 133290774 on Build GRCh38 | Gain | LOC101928193 OBP2B ABO |
dgv951n27 | Chr.9:133156364 - 133320327 on Build GRCh38 | Gain | LOC101928193 GBGT1 OBP2B ABO |
nsv615616 | Chr.9:133254625 - 133259604 on Build GRCh38 | Loss | ABO |
nsv951798 | Chr.9:133254614 - 133263597 on Build GRCh38 | Deletion | ABO |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |