Assay Details
Target Gene Details
Entrez Gene ID: | 55683 |
Gene Name: | KAT8 regulatory NSL complex subunit 3 |
Gene Aliases: |
KIAA1310, NSL3, Rcd1 |
Location: |
Chr.2:96593155-96638379 on Build GRCh38 |
Assay Gene Location: | Within Exon 27 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
KANSL3 | NM_001115016.2 | 21 | 4081 | NP_001108488.1 |
NR_047653.1 | 21 | 4142 | ||
NR_047654.1 | 21 | 4136 | ||
NR_047655.1 | 21 | 4068 | ||
NR_047656.1 | 20 | 3990 | ||
NR_047657.1 | 21 | 3936 | ||
NR_047658.1 | 20 | 3835 | ||
XM_005263984.1 | 22 | 4158 | XP_005264041.1 | |
XM_005263987.1 | 21 | 4074 | XP_005264044.1 | |
XM_017004470.1 | 22 | 4152 | XP_016859959.1 | |
XM_017004473.1 | 22 | 4171 | XP_016859962.1 | |
XM_017004474.1 | 22 | 4066 | XP_016859963.1 | |
AB037731.1 | 21 | 3888 | BAA92548.1 | |
AF311326.1 | 23 | 3888 | AAG33852.1 | |
AK000943.1 | BAA91437.1 | |||
AK023813.1 | 21 | 4103 | BAB14688.1 | |
AK074379.1 | 2 | 1591 | ||
AY050169.1 | 21 | 4109 | AAL13159.1 | |
BC051763.1 | 20 | 3790 | AAH51763.1 | |
BC063792.1 | 21 | 4011 | AAH63792.1 |
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 | KANSL3 NEURL3 ARID5A CNNM4 LMAN2L LOC105373496 FER1L5 |
nsv469775 | Chr.2:96575189 - 96746754 on Build GRCh38 | Loss | KANSL3 LMAN2L FER1L5 |
nsv834306 | Chr.2:96575378 - 96747201 on Build GRCh38 | Loss | KANSL3 LMAN2L FER1L5 |
dgv607e201 | Chr.2:95855884 - 97561622 on Build GRCh38 | Deletion | LOC105373495 STARD7-AS1 ANKRD36B FAHD2B ITPRIPL1 SEMA4C SNRNP200 CNNM3 ANKRD36 ADRA2B LOC101927053 ARID5A MIR3127 STARD7 NCAPH ASTL ANKRD39 LOC100506123 CNNM4 FAM178B CIAO1 DUSP2 LOC105373496 FER1L5 TMEM127 KANSL3 GPAT2 ANKRD23 NEURL3 LOC100506076 LOC653924 LMAN2L LOC107984110 ANKRD36C FAHD2CP |
nsv1135873 | Chr.2:95981454 - 97579645 on Build GRCh38 | Deletion | LOC105373495 STARD7-AS1 ANKRD36B FAHD2B ITPRIPL1 SEMA4C SNRNP200 CNNM3 ANKRD36 ADRA2B LOC101927053 ARID5A MIR3127 STARD7 NCAPH ASTL ANKRD39 LOC100506123 CNNM4 FAM178B CIAO1 DUSP2 LOC105373496 FER1L5 TMEM127 KANSL3 GPAT2 ANKRD23 NEURL3 LOC100506076 LOC653924 LMAN2L LOC107984110 ANKRD36C FAHD2CP |
esv3425717 | Chr.2:95859900 - 97515905 on Build GRCh38 | Duplication | LOC105373495 STARD7-AS1 ANKRD36B FAHD2B ITPRIPL1 SEMA4C SNRNP200 CNNM3 ANKRD36 ADRA2B LOC101927053 ARID5A MIR3127 STARD7 NCAPH ASTL ANKRD39 LOC100506123 CNNM4 FAM178B CIAO1 DUSP2 LOC105373496 FER1L5 TMEM127 KANSL3 GPAT2 ANKRD23 NEURL3 LOC100506076 LOC653924 LMAN2L LOC107984110 ANKRD36C FAHD2CP |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |