Assay Details
Target Gene Details
Entrez Gene ID: | 10865 |
Gene Name: | AT-rich interaction domain 5A |
Gene Aliases: |
MRF-1, MRF1, RP11-363D14 |
Location: |
Chr.2:96536719-96552638 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ARID5A | NM_001319085.1 | NP_001306014.1 | ||
NM_001319087.1 | NP_001306016.1 | |||
NM_001319092.1 | 1 | 210 | NP_001306021.1 | |
NM_001319093.1 | NP_001306022.1 | |||
NM_001319094.1 | NP_001306023.1 | |||
NM_001319096.1 | NP_001306025.1 | |||
NM_212481.2 | NP_997646.1 | |||
XM_017003183.1 | 1 | 79 | XP_016858672.1 | |
XM_017003184.1 | XP_016858673.1 | |||
XM_017003185.1 | 1 | 76 | XP_016858674.1 | |
AK300173.1 | ||||
AK304566.1 | ||||
AK307768.1 | ||||
AY358167.1 | 1 | 744 | AAQ88534.1 | |
BM556343.1 | ||||
BX396215.2 | ||||
BX648918.1 | ||||
CR981009.1 | ||||
HY002073.1 | ||||
HY076710.1 | ||||
M62324.1 | AAA36325.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2720413 | Chr.2:96472591 - 96793459 on Build GRCh38 | Deletion | LOC105373496 LMAN2L NEURL3 ARID5A FER1L5 KANSL3 CNNM4 |
dgv607e201 | Chr.2:95855884 - 97561622 on Build GRCh38 | Deletion | LOC105373496 ASTL STARD7-AS1 ANKRD36B ITPRIPL1 CIAO1 FAHD2CP ANKRD23 ANKRD36 FAM178B KANSL3 ADRA2B LOC105373495 LOC100506076 FAHD2B SEMA4C LOC100506123 LOC107984110 LOC101927053 MIR3127 CNNM4 ARID5A TMEM127 ANKRD39 SNRNP200 LOC653924 ANKRD36C CNNM3 LMAN2L DUSP2 NEURL3 GPAT2 FER1L5 STARD7 NCAPH |
nsv1135873 | Chr.2:95981454 - 97579645 on Build GRCh38 | Deletion | LOC105373496 ASTL STARD7-AS1 ANKRD36B ITPRIPL1 CIAO1 FAHD2CP ANKRD23 ANKRD36 FAM178B KANSL3 ADRA2B LOC105373495 LOC100506076 FAHD2B SEMA4C LOC100506123 LOC107984110 LOC101927053 MIR3127 CNNM4 ARID5A TMEM127 ANKRD39 SNRNP200 LOC653924 ANKRD36C CNNM3 LMAN2L DUSP2 NEURL3 GPAT2 FER1L5 STARD7 NCAPH |
esv3425717 | Chr.2:95859900 - 97515905 on Build GRCh38 | Duplication | LOC105373496 ASTL STARD7-AS1 ANKRD36B ITPRIPL1 CIAO1 FAHD2CP ANKRD23 ANKRD36 FAM178B KANSL3 ADRA2B LOC105373495 LOC100506076 FAHD2B SEMA4C LOC100506123 LOC107984110 LOC101927053 MIR3127 CNNM4 ARID5A TMEM127 ANKRD39 SNRNP200 LOC653924 ANKRD36C CNNM3 LMAN2L DUSP2 NEURL3 GPAT2 FER1L5 STARD7 NCAPH |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |