Genomic Map
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Target Gene Details
Entrez Gene ID: | 199713 |
Gene Name: | NLR family pyrin domain containing 7 |
Gene Aliases: |
CLR19.4, HYDM, NALP7, NOD12, PAN7, PYPAF3 |
Location: |
Chr.19:54923509-54965184 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NLRP7 | NM_001127255.1 | 4 | 583 | NP_001120727.1 |
| NM_139176.3 | 4 | 583 | NP_631915.2 | |
| NM_206828.3 | 4 | 583 | NP_996611.2 | |
| XM_006723075.3 | 5 | 818 | XP_006723138.1 | |
| XM_006723076.3 | 4 | 781 | XP_006723139.1 | |
| XM_011526596.2 | 6 | 1025 | XP_011524898.1 | |
| XM_011526599.2 | 6 | 1036 | XP_011524901.1 | |
| XM_011526601.2 | 6 | 1025 | XP_011524903.1 | |
| AF464765.1 | 3 | 553 | AAL69963.1 | |
| AK298630.1 | ||||
| AK302655.1 | 6 | 994 | ||
| AK313964.1 | 6 | 978 | ||
| AY154462.1 | 4 | 577 | AAO18158.1 | |
| BC109124.2 | 4 | 575 | AAI09125.1 | |
| BC109125.1 | 4 | 575 | AAI09126.1 | |
| DC425389.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv580339 | Chr.19:54930401 - 54940537 on Build GRCh38 | Loss |
 NCR1
NLRP7
|
| nsv1056824 | Chr.19:54933514 - 54976782 on Build GRCh38 | Gain |
NCR1
NLRP2
NLRP7
|
| esv2667609 | Chr.19:54472514 - 55094226 on Build GRCh38 | Deletion |
KIR2DL4
EPS8L1
KIR3DL2
LILRP2
KIR3DL3
PPP1R12C
LILRA2
NCR1
KIR2DS4
LOC101928804
NLRP2
KIR2DL1
NLRP7
GP6
KIR2DL3
KIR3DX1
LOC102724300
KIR3DL1
MIR8061
FCAR
LILRB4
RDH13
CDC42EP5
LAIR2
LILRA1
LILRB1
|
| nsv520644 | Chr.19:54889804 - 54940429 on Build GRCh38 | Loss |
NCR1
NLRP7
FCAR
|
| nsv1062047 | Chr.19:54921092 - 55041328 on Build GRCh38 | Gain |
NCR1
RDH13
NLRP2
NLRP7
GP6
|
| nsv428372 | Chr.19:54596370 - 54954956 on Build GRCh38 | Gain+Loss |
KIR3DL1
KIR2DL4
KIR3DL2
LILRP2
KIR3DL3
MIR8061
FCAR
NCR1
KIR2DS4
LILRB4
LOC101928804
KIR2DL1
NLRP7
LILRA1
LILRB1
KIR2DL3
LOC102724300
|
| esv3583572 | Chr.19:54937457 - 54998307 on Build GRCh38 | Loss |
NCR1
NLRP2
NLRP7
|
| esv2758771 | Chr.19:54163847 - 54954956 on Build GRCh38 | Gain+Loss |
MBOAT7
KIR2DL4
KIR3DL2
RPS9
TTYH1
LILRP2
KIR3DL3
TSEN34
LILRB2
LILRA2
MIR4752
LENG9
NCR1
KIR2DS4
LOC101928804
LENG8-AS1
KIR2DL1
NLRP7
LAIR1
LILRA4
LILRB5
KIR2DL3
LILRA5
KIR3DX1
TMC4
LOC102724300
KIR3DL1
MIR8061
LILRB3
LENG8
FCAR
LILRA6
LILRB4
CDC42EP5
LAIR2
LILRA1
LILRB1
|
| esv2718872 | Chr.19:54472594 - 55094247 on Build GRCh38 | Deletion |
KIR2DL4
EPS8L1
KIR3DL2
LILRP2
KIR3DL3
PPP1R12C
LILRA2
NCR1
KIR2DS4
LOC101928804
NLRP2
KIR2DL1
NLRP7
GP6
KIR2DL3
KIR3DX1
LOC102724300
KIR3DL1
MIR8061
FCAR
LILRB4
RDH13
CDC42EP5
LAIR2
LILRA1
LILRB1
|
| nsv833880 | Chr.19:54889952 - 55067343 on Build GRCh38 | Loss |
NCR1
RDH13
NLRP2
NLRP7
GP6
FCAR
|
| esv3893250 | Chr.19:54906374 - 55000768 on Build GRCh38 | Loss |
NCR1
NLRP2
NLRP7
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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