Genomic Map
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Target Gene Details
Entrez Gene ID: | 81502 |
Gene Name: | histocompatibility minor 13 |
Gene Aliases: |
H13, IMP1, IMPAS, IMPAS-1, MSTP086, PSENL3, PSL3, SPP, SPPL1 |
Location: |
Chr.20:31514410-31569567 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HM13 | NM_030789.3 | NP_110416.1 | ||
| NM_178580.2 | NP_848695.1 | |||
| NM_178581.2 | NP_848696.1 | |||
| NM_178582.2 | NP_848697.1 | |||
| AF172086.1 | AAQ13609.1 | |||
| AF483215.1 | AAM22076.1 | |||
| AF515663.1 | AAN77099.1 | |||
| AJ345029.1 | CAC87790.1 | |||
| AJ420895.1 | CAD13132.1 | |||
| AK074686.1 | BAC11138.1 | |||
| AK075283.1 | BAC11519.1 | |||
| AK314410.1 | ||||
| AY169310.1 | AAO12535.1 | |||
| AY169311.1 | AAO12536.1 | |||
| AY169312.1 | AAO12537.1 | |||
| BC008938.2 | AAH08938.1 | |||
| BC008959.2 | AAH08959.1 | |||
| BC062595.1 | AAH62595.1 | |||
| BI192962.1 | ||||
| BI552780.1 | ||||
| DA087240.1 | ||||
| DQ168450.1 | ||||
| KU178790.1 | ||||
| KU178791.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv470546 | Chr.20:31245806 - 31647499 on Build GRCh38 | Gain |
 ID1
DEFB115
DEFB119
LOC107985416
MIR3193
REM1
COX4I2
DEFB122
DEFB117
DEFB116
HM13-AS1
HM13
DEFB118
LINC00028
DEFB121
DEFB123
DEFB124
|
| nsv1118664 | Chr.20:31536497 - 31538997 on Build GRCh38 | Duplication |
HM13
|
| esv3645653 | Chr.20:31535328 - 31555299 on Build GRCh38 | Gain |
HM13
|
| dgv4300n100 | Chr.20:31247234 - 32033468 on Build GRCh38 | Gain |
ID1
DEFB115
LOC107985416
MIR3193
REM1
COX4I2
BCL2L1
DEFB117
DEFB116
HM13-AS1
HM13
LINC00028
DEFB123
DEFB124
MYLK2
XKR7
DUSP15
DEFB119
PDRG1
TPX2
FOXS1
CCM2L
DEFB122
DEFB118
ABALON
TTLL9
DEFB121
|
| esv2763228 | Chr.20:31247246 - 31651719 on Build GRCh38 | Gain |
ID1
DEFB115
DEFB119
LOC107985416
MIR3193
REM1
COX4I2
DEFB122
DEFB117
DEFB116
HM13-AS1
HM13
DEFB118
LINC00028
DEFB121
DEFB123
DEFB124
|
| esv3645652 | Chr.20:31500710 - 31576564 on Build GRCh38 | Gain |
HM13-AS1
HM13
LOC107985416
|
| nsv585911 | Chr.20:31305698 - 31688103 on Build GRCh38 | Gain |
ID1
DEFB119
LOC107985416
MIR3193
REM1
COX4I2
BCL2L1
DEFB122
DEFB117
DEFB116
HM13-AS1
HM13
DEFB118
LINC00028
DEFB121
DEFB123
DEFB124
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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