Genomic Map
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Target Gene Details
Entrez Gene ID: | 55655 |
Gene Name: | NLR family pyrin domain containing 2 |
Gene Aliases: |
CLR19.9, NALP2, NBS1, PAN1, PYPAF2 |
Location: |
Chr.19:54965284-55001142 on Build GRCh38 |
Assay Gene Location: | Within Intron 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NLRP2 | NM_001174081.1 | NP_001167552.1 | ||
| NM_001174082.1 | NP_001167553.1 | |||
| NM_001174083.1 | NP_001167554.1 | |||
| NM_017852.3 | NP_060322.1 | |||
| AB209300.1 | BAD92537.1 | |||
| AF269288.2 | 1 | 166 | AAG23171.2 | |
| AF298547.1 | AAG15253.1 | |||
| AF310106.1 | AAG30289.1 | |||
| AF464764.1 | AAL69962.1 | |||
| AK000517.1 | BAA91223.1 | |||
| AK000784.1 | BAA91377.1 | |||
| AK025952.1 | BAB15293.1 | |||
| AK223253.1 | BAD96973.1 | |||
| AK223269.1 | BAD96989.1 | |||
| AK292681.1 | ||||
| AK302989.1 | ||||
| BC001039.2 | AAH01039.1 | |||
| BC003592.1 | AAH03592.1 | |||
| BC039269.1 | AAH39269.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3644827 | Chr.19:54976334 - 55017364 on Build GRCh38 | Loss |
 NLRP2
GP6
|
| esv2667609 | Chr.19:54472514 - 55094226 on Build GRCh38 | Deletion |
NLRP7
LILRB1
NCR1
KIR2DL4
FCAR
KIR2DS4
KIR2DL3
KIR3DX1
PPP1R12C
NLRP2
EPS8L1
LILRB4
KIR2DL1
LILRA1
LOC102724300
CDC42EP5
KIR3DL3
MIR8061
LOC101928804
LILRA2
KIR3DL1
KIR3DL2
LAIR2
RDH13
LILRP2
GP6
|
| dgv3679n100 | Chr.19:54944244 - 55017462 on Build GRCh38 | Loss |
NLRP7
NLRP2
GP6
|
| nsv580341 | Chr.19:54973805 - 55048372 on Build GRCh38 | Loss |
RDH13
NLRP2
GP6
|
| nsv1062047 | Chr.19:54921092 - 55041328 on Build GRCh38 | Gain |
NLRP7
NCR1
RDH13
NLRP2
GP6
|
| esv3583572 | Chr.19:54937457 - 54998307 on Build GRCh38 | Loss |
NLRP7
NCR1
NLRP2
|
| esv2659880 | Chr.19:54976502 - 55017273 on Build GRCh38 | Deletion |
NLRP2
GP6
|
| esv3583573 | Chr.19:54992924 - 55013445 on Build GRCh38 | Loss |
NLRP2
|
| nsv833880 | Chr.19:54889952 - 55067343 on Build GRCh38 | Loss |
NLRP7
NCR1
FCAR
RDH13
NLRP2
GP6
|
| esv2718872 | Chr.19:54472594 - 55094247 on Build GRCh38 | Deletion |
NLRP7
LILRB1
NCR1
KIR2DL4
FCAR
KIR2DS4
KIR2DL3
KIR3DX1
PPP1R12C
NLRP2
EPS8L1
LILRB4
KIR2DL1
LILRA1
LOC102724300
CDC42EP5
KIR3DL3
MIR8061
LOC101928804
LILRA2
KIR3DL1
KIR3DL2
LAIR2
RDH13
LILRP2
GP6
|
| esv3893250 | Chr.19:54906374 - 55000768 on Build GRCh38 | Loss |
NLRP7
NCR1
NLRP2
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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