Incidental Mutation 'R5644:Nlrp9a'
ID |
440957 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nlrp9a
|
Ensembl Gene |
ENSMUSG00000054102 |
Gene Name |
NLR family, pyrin domain containing 9A |
Synonyms |
Nalp9a, Nalp-theta, D7Ertd565e |
MMRRC Submission |
043292-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.060)
|
Stock # |
R5644 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
26234448-26273573 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 26257993 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Leucine
at position 537
(H537L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112398
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071780]
[ENSMUST00000108387]
[ENSMUST00000117252]
[ENSMUST00000122040]
[ENSMUST00000153452]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000071780
AA Change: H537L
PolyPhen 2
Score 0.035 (Sensitivity: 0.94; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000071685 Gene: ENSMUSG00000054102 AA Change: H537L
Domain | Start | End | E-Value | Type |
PYRIN
|
5 |
87 |
1.07e-25 |
SMART |
Pfam:NACHT
|
143 |
311 |
1e-32 |
PFAM |
LRR
|
637 |
664 |
1.42e0 |
SMART |
LRR
|
693 |
720 |
2.32e-1 |
SMART |
LRR
|
722 |
749 |
3e0 |
SMART |
LRR
|
750 |
777 |
1.12e-3 |
SMART |
LRR
|
779 |
806 |
2.17e0 |
SMART |
LRR
|
807 |
834 |
2.27e-4 |
SMART |
LRR
|
836 |
863 |
2.02e2 |
SMART |
LRR
|
864 |
891 |
6.24e1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108387
AA Change: H537L
PolyPhen 2
Score 0.035 (Sensitivity: 0.94; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000104024 Gene: ENSMUSG00000054102 AA Change: H537L
Domain | Start | End | E-Value | Type |
PYRIN
|
5 |
87 |
1.07e-25 |
SMART |
Pfam:NACHT
|
143 |
311 |
7.7e-33 |
PFAM |
LRR
|
631 |
658 |
1.42e0 |
SMART |
LRR
|
692 |
719 |
1.42e0 |
SMART |
LRR
|
748 |
775 |
2.32e-1 |
SMART |
LRR
|
777 |
804 |
3e0 |
SMART |
LRR
|
805 |
832 |
1.12e-3 |
SMART |
LRR
|
834 |
861 |
2.17e0 |
SMART |
LRR
|
862 |
889 |
2.27e-4 |
SMART |
LRR
|
891 |
918 |
2.02e2 |
SMART |
LRR
|
919 |
946 |
6.24e1 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000117252
AA Change: H537L
PolyPhen 2
Score 0.508 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000112398 Gene: ENSMUSG00000054102 AA Change: H537L
Domain | Start | End | E-Value | Type |
PYRIN
|
5 |
87 |
1.07e-25 |
SMART |
Pfam:NACHT
|
143 |
311 |
8.8e-34 |
PFAM |
LRR
|
637 |
664 |
1.42e0 |
SMART |
Blast:LRR
|
666 |
692 |
1e-5 |
BLAST |
LRR
|
693 |
720 |
2.32e-1 |
SMART |
LRR
|
722 |
749 |
3e0 |
SMART |
LRR
|
750 |
777 |
1.12e-3 |
SMART |
LRR
|
779 |
806 |
2.39e0 |
SMART |
LRR
|
807 |
834 |
6.24e1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000122040
AA Change: H537L
PolyPhen 2
Score 0.035 (Sensitivity: 0.94; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000113318 Gene: ENSMUSG00000054102 AA Change: H537L
Domain | Start | End | E-Value | Type |
PYRIN
|
5 |
87 |
1.07e-25 |
SMART |
Pfam:NACHT
|
143 |
311 |
1e-32 |
PFAM |
LRR
|
637 |
664 |
1.42e0 |
SMART |
LRR
|
693 |
720 |
2.32e-1 |
SMART |
LRR
|
722 |
749 |
3e0 |
SMART |
LRR
|
750 |
777 |
1.12e-3 |
SMART |
LRR
|
779 |
806 |
2.17e0 |
SMART |
LRR
|
807 |
834 |
2.27e-4 |
SMART |
LRR
|
836 |
863 |
2.02e2 |
SMART |
LRR
|
864 |
891 |
6.24e1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000143149
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000153452
AA Change: H448L
PolyPhen 2
Score 0.080 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000120498 Gene: ENSMUSG00000054102 AA Change: H448L
Domain | Start | End | E-Value | Type |
Pfam:NACHT
|
54 |
222 |
6.9e-33 |
PFAM |
LRR
|
542 |
569 |
1.42e0 |
SMART |
LRR
|
603 |
630 |
1.42e0 |
SMART |
Blast:LRR
|
632 |
657 |
1e-5 |
BLAST |
LRR
|
659 |
686 |
2.32e-1 |
SMART |
LRR
|
688 |
715 |
3e0 |
SMART |
LRR
|
716 |
743 |
1.12e-3 |
SMART |
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.5%
- 20x: 95.8%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
A |
T |
10: 14,308,678 (GRCm39) |
D805E |
probably damaging |
Het |
Adrb2 |
A |
T |
18: 62,311,753 (GRCm39) |
N357K |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,988,021 (GRCm39) |
K3102E |
possibly damaging |
Het |
Alkal2 |
T |
A |
12: 30,934,889 (GRCm39) |
L36Q |
probably damaging |
Het |
Alkbh8 |
G |
T |
9: 3,385,384 (GRCm39) |
V559F |
probably damaging |
Het |
Apba2 |
A |
G |
7: 64,365,259 (GRCm39) |
T346A |
probably benign |
Het |
Arhgap10 |
C |
T |
8: 78,137,684 (GRCm39) |
M302I |
probably benign |
Het |
Asah1 |
G |
T |
8: 41,813,332 (GRCm39) |
T27K |
possibly damaging |
Het |
Bag2 |
A |
G |
1: 33,786,034 (GRCm39) |
V96A |
probably damaging |
Het |
Bicd1 |
C |
T |
6: 149,421,901 (GRCm39) |
A874V |
probably damaging |
Het |
C4b |
T |
C |
17: 34,961,391 (GRCm39) |
I189M |
probably benign |
Het |
Cacna1a |
A |
G |
8: 85,189,406 (GRCm39) |
Y119C |
probably damaging |
Het |
Calcr |
A |
G |
6: 3,708,538 (GRCm39) |
I216T |
probably damaging |
Het |
Ccar1 |
T |
C |
10: 62,607,757 (GRCm39) |
N302S |
probably benign |
Het |
Ccdc93 |
A |
G |
1: 121,411,065 (GRCm39) |
H446R |
probably benign |
Het |
Cct6b |
A |
T |
11: 82,613,281 (GRCm39) |
L420Q |
probably benign |
Het |
Cemip |
T |
C |
7: 83,638,392 (GRCm39) |
T273A |
probably benign |
Het |
Cep128 |
A |
T |
12: 91,315,625 (GRCm39) |
I87K |
probably damaging |
Het |
Cfap221 |
A |
G |
1: 119,860,532 (GRCm39) |
L698P |
probably damaging |
Het |
Cfap43 |
T |
A |
19: 47,784,114 (GRCm39) |
N473I |
possibly damaging |
Het |
Clec12b |
T |
A |
6: 129,356,923 (GRCm39) |
I172L |
probably benign |
Het |
Cntnap5b |
A |
C |
1: 100,311,326 (GRCm39) |
E606D |
probably benign |
Het |
Cyp2c67 |
A |
C |
19: 39,604,138 (GRCm39) |
V406G |
possibly damaging |
Het |
Dhx57 |
T |
C |
17: 80,546,302 (GRCm39) |
I1308V |
possibly damaging |
Het |
Dnah7a |
A |
T |
1: 53,580,138 (GRCm39) |
M1599K |
probably benign |
Het |
Dnajc21 |
A |
T |
15: 10,462,001 (GRCm39) |
D133E |
probably benign |
Het |
Dpp8 |
G |
A |
9: 64,953,017 (GRCm39) |
W231* |
probably null |
Het |
Dvl3 |
T |
A |
16: 20,345,026 (GRCm39) |
I353N |
probably damaging |
Het |
Fgd6 |
T |
A |
10: 93,969,912 (GRCm39) |
I1187N |
possibly damaging |
Het |
Fn1 |
A |
T |
1: 71,666,409 (GRCm39) |
Y875N |
probably damaging |
Het |
Gaa |
T |
A |
11: 119,171,361 (GRCm39) |
M671K |
possibly damaging |
Het |
Gm11939 |
T |
C |
11: 99,450,138 (GRCm39) |
D52G |
probably damaging |
Het |
Gm14403 |
A |
T |
2: 177,199,054 (GRCm39) |
H50L |
possibly damaging |
Het |
Gpam |
A |
T |
19: 55,077,331 (GRCm39) |
D153E |
probably benign |
Het |
Gzma |
T |
C |
13: 113,234,794 (GRCm39) |
T66A |
probably damaging |
Het |
Hnmt |
A |
T |
2: 23,904,251 (GRCm39) |
W137R |
probably damaging |
Het |
Hsd17b7 |
A |
T |
1: 169,783,517 (GRCm39) |
V297D |
probably damaging |
Het |
Ighv1-85 |
A |
T |
12: 115,963,680 (GRCm39) |
S107T |
possibly damaging |
Het |
Kif12 |
T |
A |
4: 63,084,130 (GRCm39) |
Q624L |
possibly damaging |
Het |
Kif1b |
T |
C |
4: 149,322,939 (GRCm39) |
D660G |
probably damaging |
Het |
Klf13 |
T |
C |
7: 63,541,308 (GRCm39) |
|
probably benign |
Het |
Klhl41 |
A |
G |
2: 69,500,815 (GRCm39) |
Y92C |
probably damaging |
Het |
Klrc2 |
A |
T |
6: 129,633,420 (GRCm39) |
C186S |
probably damaging |
Het |
Lao1 |
T |
A |
4: 118,822,433 (GRCm39) |
|
probably null |
Het |
Lmo7 |
A |
G |
14: 102,166,772 (GRCm39) |
|
probably benign |
Het |
Lyst |
A |
T |
13: 13,812,081 (GRCm39) |
Q831L |
possibly damaging |
Het |
Lzts1 |
A |
G |
8: 69,591,729 (GRCm39) |
S140P |
possibly damaging |
Het |
Man2b1 |
T |
A |
8: 85,820,839 (GRCm39) |
I679N |
possibly damaging |
Het |
Mgat5b |
T |
A |
11: 116,864,226 (GRCm39) |
V464E |
probably damaging |
Het |
Mrgprb5 |
G |
A |
7: 47,817,955 (GRCm39) |
T260I |
probably benign |
Het |
Mybpc2 |
T |
C |
7: 44,156,477 (GRCm39) |
T825A |
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,524,770 (GRCm39) |
K597I |
probably damaging |
Het |
Naalad2 |
G |
T |
9: 18,246,227 (GRCm39) |
N568K |
possibly damaging |
Het |
Neurl1a |
A |
G |
19: 47,167,916 (GRCm39) |
N4S |
probably benign |
Het |
Nfx1 |
T |
C |
4: 40,984,973 (GRCm39) |
W366R |
probably null |
Het |
Nipbl |
C |
T |
15: 8,388,391 (GRCm39) |
V410I |
probably benign |
Het |
Nxpe4 |
A |
G |
9: 48,304,050 (GRCm39) |
N46D |
probably benign |
Het |
Or14j10 |
T |
A |
17: 37,935,323 (GRCm39) |
I68F |
probably benign |
Het |
Or4c101 |
T |
A |
2: 88,389,849 (GRCm39) |
M1K |
probably null |
Het |
Or4f60 |
A |
T |
2: 111,902,013 (GRCm39) |
M305K |
probably benign |
Het |
Or5ae1 |
C |
A |
7: 84,565,327 (GRCm39) |
F113L |
probably benign |
Het |
Or5b95 |
A |
T |
19: 12,658,336 (GRCm39) |
Y288F |
probably damaging |
Het |
Or5p58 |
A |
T |
7: 107,694,011 (GRCm39) |
Y255* |
probably null |
Het |
Or5p60 |
A |
G |
7: 107,723,858 (GRCm39) |
F204S |
probably benign |
Het |
Or6c2 |
A |
T |
10: 129,362,972 (GRCm39) |
N292I |
probably damaging |
Het |
Or6c76b |
T |
A |
10: 129,693,296 (GRCm39) |
V303E |
probably benign |
Het |
Or8u10 |
T |
C |
2: 85,915,503 (GRCm39) |
N206S |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,125,516 (GRCm39) |
M53K |
possibly damaging |
Het |
Pcca |
G |
A |
14: 123,124,481 (GRCm39) |
C684Y |
probably damaging |
Het |
Pdzd7 |
A |
G |
19: 45,028,619 (GRCm39) |
S175P |
probably benign |
Het |
Pgbd1 |
A |
G |
13: 21,607,322 (GRCm39) |
C291R |
probably damaging |
Het |
Plekhg5 |
T |
C |
4: 152,188,797 (GRCm39) |
V200A |
probably benign |
Het |
Pola2 |
A |
G |
19: 6,011,198 (GRCm39) |
V42A |
probably benign |
Het |
Pramel16 |
C |
T |
4: 143,675,374 (GRCm39) |
G484D |
probably benign |
Het |
Prkcd |
C |
A |
14: 30,329,370 (GRCm39) |
K23N |
probably benign |
Het |
Ptdss1 |
T |
C |
13: 67,120,604 (GRCm39) |
F267L |
probably damaging |
Het |
Rad54l |
C |
T |
4: 115,956,144 (GRCm39) |
S561N |
probably benign |
Het |
Rai14 |
T |
A |
15: 10,593,137 (GRCm39) |
H169L |
probably benign |
Het |
Rfc3 |
C |
T |
5: 151,573,444 (GRCm39) |
V40I |
probably benign |
Het |
Rpl31 |
C |
T |
1: 39,409,108 (GRCm39) |
R41C |
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,558,013 (GRCm39) |
M1275I |
probably benign |
Het |
Ryr2 |
C |
A |
13: 11,610,468 (GRCm39) |
E4119D |
probably damaging |
Het |
Senp7 |
T |
C |
16: 56,004,512 (GRCm39) |
|
silent |
Het |
Sfmbt2 |
A |
T |
2: 10,573,184 (GRCm39) |
I571F |
probably damaging |
Het |
Sit1 |
T |
A |
4: 43,483,562 (GRCm39) |
T8S |
probably benign |
Het |
Slc22a30 |
T |
C |
19: 8,381,980 (GRCm39) |
H97R |
possibly damaging |
Het |
Slco1a5 |
A |
C |
6: 142,183,320 (GRCm39) |
|
probably null |
Het |
Smc6 |
T |
A |
12: 11,339,995 (GRCm39) |
N434K |
probably benign |
Het |
Snap91 |
G |
T |
9: 86,672,206 (GRCm39) |
|
probably null |
Het |
Srsf10 |
T |
C |
4: 135,591,131 (GRCm39) |
S194P |
possibly damaging |
Het |
St14 |
T |
C |
9: 31,017,806 (GRCm39) |
M205V |
probably benign |
Het |
Syndig1 |
A |
T |
2: 149,741,428 (GRCm39) |
I5F |
possibly damaging |
Het |
Tbrg1 |
T |
C |
9: 37,560,709 (GRCm39) |
D389G |
probably benign |
Het |
Tcaf2 |
G |
A |
6: 42,619,707 (GRCm39) |
R107C |
possibly damaging |
Het |
Tpmt |
T |
A |
13: 47,182,435 (GRCm39) |
D163V |
probably benign |
Het |
Trim15 |
T |
C |
17: 37,177,713 (GRCm39) |
E94G |
probably damaging |
Het |
Trit1 |
T |
C |
4: 122,942,965 (GRCm39) |
I279T |
probably damaging |
Het |
Trpm8 |
T |
A |
1: 88,287,461 (GRCm39) |
F815I |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,768,867 (GRCm39) |
T2856S |
probably damaging |
Het |
Ugdh |
A |
T |
5: 65,574,204 (GRCm39) |
D446E |
probably benign |
Het |
Unc5c |
C |
T |
3: 141,383,886 (GRCm39) |
A88V |
probably damaging |
Het |
Vmn1r43 |
T |
C |
6: 89,847,354 (GRCm39) |
N44S |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,977 (GRCm39) |
M271L |
probably benign |
Het |
Wdr74 |
T |
A |
19: 8,715,240 (GRCm39) |
V133E |
probably damaging |
Het |
Zfp607b |
T |
C |
7: 27,403,194 (GRCm39) |
L550P |
probably damaging |
Het |
|
Other mutations in Nlrp9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Nlrp9a
|
APN |
7 |
26,257,050 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00895:Nlrp9a
|
APN |
7 |
26,258,103 (GRCm39) |
missense |
probably benign |
|
IGL01081:Nlrp9a
|
APN |
7 |
26,257,519 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01148:Nlrp9a
|
APN |
7 |
26,257,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01368:Nlrp9a
|
APN |
7 |
26,257,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01914:Nlrp9a
|
APN |
7 |
26,256,689 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01952:Nlrp9a
|
APN |
7 |
26,257,444 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02245:Nlrp9a
|
APN |
7 |
26,257,318 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02449:Nlrp9a
|
APN |
7 |
26,264,396 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02702:Nlrp9a
|
APN |
7 |
26,264,381 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02944:Nlrp9a
|
APN |
7 |
26,258,076 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03183:Nlrp9a
|
APN |
7 |
26,256,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0005:Nlrp9a
|
UTSW |
7 |
26,273,213 (GRCm39) |
splice site |
probably benign |
|
R0007:Nlrp9a
|
UTSW |
7 |
26,250,515 (GRCm39) |
intron |
probably benign |
|
R0007:Nlrp9a
|
UTSW |
7 |
26,250,515 (GRCm39) |
intron |
probably benign |
|
R0013:Nlrp9a
|
UTSW |
7 |
26,270,650 (GRCm39) |
splice site |
probably null |
|
R0086:Nlrp9a
|
UTSW |
7 |
26,257,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R0659:Nlrp9a
|
UTSW |
7 |
26,256,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R1126:Nlrp9a
|
UTSW |
7 |
26,260,166 (GRCm39) |
missense |
probably benign |
0.12 |
R1500:Nlrp9a
|
UTSW |
7 |
26,267,316 (GRCm39) |
missense |
probably benign |
0.01 |
R1585:Nlrp9a
|
UTSW |
7 |
26,258,093 (GRCm39) |
missense |
probably benign |
0.41 |
R1594:Nlrp9a
|
UTSW |
7 |
26,269,932 (GRCm39) |
nonsense |
probably null |
|
R1968:Nlrp9a
|
UTSW |
7 |
26,264,366 (GRCm39) |
missense |
probably benign |
0.23 |
R1989:Nlrp9a
|
UTSW |
7 |
26,273,338 (GRCm39) |
missense |
probably benign |
0.24 |
R2057:Nlrp9a
|
UTSW |
7 |
26,256,787 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2058:Nlrp9a
|
UTSW |
7 |
26,256,787 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2059:Nlrp9a
|
UTSW |
7 |
26,256,787 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2188:Nlrp9a
|
UTSW |
7 |
26,264,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R2318:Nlrp9a
|
UTSW |
7 |
26,273,277 (GRCm39) |
missense |
probably damaging |
0.98 |
R3110:Nlrp9a
|
UTSW |
7 |
26,257,297 (GRCm39) |
missense |
probably benign |
0.08 |
R3112:Nlrp9a
|
UTSW |
7 |
26,257,297 (GRCm39) |
missense |
probably benign |
0.08 |
R3237:Nlrp9a
|
UTSW |
7 |
26,270,810 (GRCm39) |
nonsense |
probably null |
|
R3545:Nlrp9a
|
UTSW |
7 |
26,256,757 (GRCm39) |
missense |
probably benign |
0.03 |
R3805:Nlrp9a
|
UTSW |
7 |
26,264,277 (GRCm39) |
nonsense |
probably null |
|
R4005:Nlrp9a
|
UTSW |
7 |
26,257,975 (GRCm39) |
missense |
probably benign |
0.02 |
R4057:Nlrp9a
|
UTSW |
7 |
26,270,071 (GRCm39) |
missense |
probably benign |
0.00 |
R4529:Nlrp9a
|
UTSW |
7 |
26,270,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R4756:Nlrp9a
|
UTSW |
7 |
26,256,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Nlrp9a
|
UTSW |
7 |
26,250,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Nlrp9a
|
UTSW |
7 |
26,269,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Nlrp9a
|
UTSW |
7 |
26,256,811 (GRCm39) |
missense |
probably benign |
0.00 |
R5042:Nlrp9a
|
UTSW |
7 |
26,270,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R5224:Nlrp9a
|
UTSW |
7 |
26,256,717 (GRCm39) |
missense |
probably benign |
0.43 |
R5449:Nlrp9a
|
UTSW |
7 |
26,257,254 (GRCm39) |
missense |
probably benign |
0.04 |
R5734:Nlrp9a
|
UTSW |
7 |
26,270,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Nlrp9a
|
UTSW |
7 |
26,257,762 (GRCm39) |
missense |
probably benign |
0.02 |
R5978:Nlrp9a
|
UTSW |
7 |
26,256,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Nlrp9a
|
UTSW |
7 |
26,257,762 (GRCm39) |
missense |
probably benign |
0.02 |
R6066:Nlrp9a
|
UTSW |
7 |
26,257,510 (GRCm39) |
missense |
probably benign |
0.00 |
R6082:Nlrp9a
|
UTSW |
7 |
26,267,402 (GRCm39) |
missense |
probably benign |
0.41 |
R6171:Nlrp9a
|
UTSW |
7 |
26,258,188 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6352:Nlrp9a
|
UTSW |
7 |
26,257,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Nlrp9a
|
UTSW |
7 |
26,250,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6540:Nlrp9a
|
UTSW |
7 |
26,256,817 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7039:Nlrp9a
|
UTSW |
7 |
26,267,367 (GRCm39) |
missense |
probably benign |
0.03 |
R7151:Nlrp9a
|
UTSW |
7 |
26,256,672 (GRCm39) |
nonsense |
probably null |
|
R7173:Nlrp9a
|
UTSW |
7 |
26,257,603 (GRCm39) |
missense |
probably benign |
0.00 |
R7214:Nlrp9a
|
UTSW |
7 |
26,250,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R7226:Nlrp9a
|
UTSW |
7 |
26,258,149 (GRCm39) |
missense |
probably benign |
0.02 |
R7250:Nlrp9a
|
UTSW |
7 |
26,258,143 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7293:Nlrp9a
|
UTSW |
7 |
26,270,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R7492:Nlrp9a
|
UTSW |
7 |
26,257,081 (GRCm39) |
missense |
probably damaging |
0.99 |
R7586:Nlrp9a
|
UTSW |
7 |
26,256,721 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7844:Nlrp9a
|
UTSW |
7 |
26,262,006 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8073:Nlrp9a
|
UTSW |
7 |
26,260,260 (GRCm39) |
missense |
probably damaging |
0.98 |
R8136:Nlrp9a
|
UTSW |
7 |
26,256,678 (GRCm39) |
missense |
probably benign |
0.34 |
R8400:Nlrp9a
|
UTSW |
7 |
26,264,431 (GRCm39) |
missense |
probably benign |
0.02 |
R8415:Nlrp9a
|
UTSW |
7 |
26,256,925 (GRCm39) |
missense |
probably benign |
|
R8774:Nlrp9a
|
UTSW |
7 |
26,257,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8774-TAIL:Nlrp9a
|
UTSW |
7 |
26,257,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8882:Nlrp9a
|
UTSW |
7 |
26,257,703 (GRCm39) |
nonsense |
probably null |
|
R9023:Nlrp9a
|
UTSW |
7 |
26,273,291 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9031:Nlrp9a
|
UTSW |
7 |
26,257,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R9063:Nlrp9a
|
UTSW |
7 |
26,273,291 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9090:Nlrp9a
|
UTSW |
7 |
26,261,944 (GRCm39) |
missense |
probably benign |
|
R9196:Nlrp9a
|
UTSW |
7 |
26,258,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9206:Nlrp9a
|
UTSW |
7 |
26,257,656 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9265:Nlrp9a
|
UTSW |
7 |
26,258,038 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9271:Nlrp9a
|
UTSW |
7 |
26,261,944 (GRCm39) |
missense |
probably benign |
|
R9384:Nlrp9a
|
UTSW |
7 |
26,258,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Nlrp9a
|
UTSW |
7 |
26,270,030 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9424:Nlrp9a
|
UTSW |
7 |
26,260,178 (GRCm39) |
missense |
probably benign |
0.13 |
R9620:Nlrp9a
|
UTSW |
7 |
26,250,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Nlrp9a
|
UTSW |
7 |
26,256,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R9696:Nlrp9a
|
UTSW |
7 |
26,275,033 (GRCm39) |
missense |
unknown |
|
R9728:Nlrp9a
|
UTSW |
7 |
26,256,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R9744:Nlrp9a
|
UTSW |
7 |
26,267,266 (GRCm39) |
missense |
probably benign |
0.07 |
R9794:Nlrp9a
|
UTSW |
7 |
26,264,302 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Nlrp9a
|
UTSW |
7 |
26,257,654 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nlrp9a
|
UTSW |
7 |
26,256,881 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ATTGGAAACCTCGCTCAACTC -3'
(R):5'- CTCTCTTTTGTATATGCAGGTGAAG -3'
Sequencing Primer
(F):5'- GCTCAACTCCTAGGAGAAATCTATG -3'
(R):5'- AAGGTTTTTCACTTTTGGGGCTC -3'
|
Posted On |
2016-11-08 |