Incidental Mutation 'R7293:Nlrp9a'
ID |
566549 |
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 |
045398-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.070)
|
Stock # |
R7293 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
26234448-26273573 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 26270694 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Tyrosine
at position 908
(C908Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000104024
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071780]
[ENSMUST00000108387]
[ENSMUST00000117252]
[ENSMUST00000122040]
[ENSMUST00000153452]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000071780
AA Change: C853Y
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000071685 Gene: ENSMUSG00000054102 AA Change: C853Y
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 damaging
Transcript: ENSMUST00000108387
AA Change: C908Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000104024 Gene: ENSMUSG00000054102 AA Change: C908Y
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 |
probably damaging
Transcript: ENSMUST00000117252
AA Change: C796Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000112398 Gene: ENSMUSG00000054102 AA Change: C796Y
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 damaging
Transcript: ENSMUST00000122040
AA Change: C853Y
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113318 Gene: ENSMUSG00000054102 AA Change: C853Y
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: ENSMUST00000153452
|
SMART Domains |
Protein: ENSMUSP00000120498 Gene: ENSMUSG00000054102
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 |
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
97% (74/76) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
G |
A |
19: 43,795,492 (GRCm39) |
G416E |
probably damaging |
Het |
Acsl5 |
G |
T |
19: 55,279,642 (GRCm39) |
W460L |
probably damaging |
Het |
Adam2 |
A |
G |
14: 66,272,634 (GRCm39) |
F614S |
probably benign |
Het |
Adamts5 |
G |
A |
16: 85,696,833 (GRCm39) |
T108I |
probably benign |
Het |
Agmat |
C |
T |
4: 141,483,246 (GRCm39) |
Q227* |
probably null |
Het |
Alg11 |
A |
G |
8: 22,555,395 (GRCm39) |
N219D |
probably damaging |
Het |
Amhr2 |
A |
G |
15: 102,355,828 (GRCm39) |
T258A |
probably benign |
Het |
Ankrd53 |
A |
G |
6: 83,740,178 (GRCm39) |
E82G |
probably null |
Het |
Blzf1 |
T |
A |
1: 164,123,452 (GRCm39) |
T292S |
possibly damaging |
Het |
Capza1 |
T |
C |
3: 104,748,151 (GRCm39) |
D71G |
probably benign |
Het |
Cc2d1b |
T |
C |
4: 108,488,873 (GRCm39) |
F770L |
probably benign |
Het |
Cckbr |
A |
T |
7: 105,083,852 (GRCm39) |
Q260L |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,085,836 (GRCm39) |
T1163A |
probably benign |
Het |
Chd9 |
T |
C |
8: 91,760,707 (GRCm39) |
S2151P |
unknown |
Het |
Clk1 |
T |
A |
1: 58,453,772 (GRCm39) |
T301S |
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,229,305 (GRCm39) |
S1928C |
possibly damaging |
Het |
Col24a1 |
C |
T |
3: 145,192,059 (GRCm39) |
Q1273* |
probably null |
Het |
Col4a4 |
T |
C |
1: 82,501,664 (GRCm39) |
D363G |
unknown |
Het |
Copb1 |
A |
T |
7: 113,818,837 (GRCm39) |
M827K |
probably damaging |
Het |
Crocc |
C |
T |
4: 140,770,867 (GRCm39) |
A351T |
probably benign |
Het |
Crybg1 |
T |
C |
10: 43,879,428 (GRCm39) |
T587A |
probably damaging |
Het |
Csrnp3 |
A |
G |
2: 65,779,344 (GRCm39) |
R19G |
probably damaging |
Het |
Cyb5rl |
T |
C |
4: 106,938,143 (GRCm39) |
I165T |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 31,009,820 (GRCm39) |
I1916N |
probably damaging |
Het |
Dvl1 |
T |
C |
4: 155,940,625 (GRCm39) |
M415T |
possibly damaging |
Het |
Dync2h1 |
A |
G |
9: 7,001,454 (GRCm39) |
S3845P |
possibly damaging |
Het |
Eif3b |
A |
G |
5: 140,405,183 (GRCm39) |
Q23R |
probably benign |
Het |
Esam |
G |
T |
9: 37,449,020 (GRCm39) |
R376L |
probably damaging |
Het |
Fat3 |
G |
C |
9: 15,826,336 (GRCm39) |
H391D |
|
Het |
Fat3 |
A |
C |
9: 15,826,592 (GRCm39) |
S305R |
|
Het |
Fgd3 |
T |
C |
13: 49,418,134 (GRCm39) |
D644G |
probably benign |
Het |
Fgf7 |
T |
C |
2: 125,877,672 (GRCm39) |
L13P |
probably damaging |
Het |
Gas2l1 |
A |
G |
11: 5,014,338 (GRCm39) |
Y41H |
probably damaging |
Het |
Glg1 |
A |
T |
8: 111,895,375 (GRCm39) |
I812N |
probably damaging |
Het |
Glp1r |
C |
T |
17: 31,143,599 (GRCm39) |
H212Y |
probably benign |
Het |
Gm5622 |
G |
T |
14: 51,893,339 (GRCm39) |
E89* |
probably null |
Het |
Gpr158 |
G |
A |
2: 21,581,750 (GRCm39) |
V410I |
possibly damaging |
Het |
Ighv1-53 |
A |
T |
12: 115,122,441 (GRCm39) |
C5* |
probably null |
Het |
Itgb2l |
A |
C |
16: 96,227,996 (GRCm39) |
Y502* |
probably null |
Het |
Jakmip1 |
G |
A |
5: 37,284,817 (GRCm39) |
V635I |
probably benign |
Het |
Kplce |
A |
T |
3: 92,776,126 (GRCm39) |
C186S |
probably benign |
Het |
Krt23 |
C |
T |
11: 99,374,682 (GRCm39) |
M270I |
probably benign |
Het |
Larp1b |
C |
T |
3: 40,939,879 (GRCm39) |
A344V |
|
Het |
Lin28b |
T |
C |
10: 45,295,282 (GRCm39) |
M134V |
probably benign |
Het |
Lrrc19 |
T |
A |
4: 94,526,627 (GRCm39) |
Y310F |
probably benign |
Het |
Lyst |
T |
A |
13: 13,854,822 (GRCm39) |
D2397E |
probably benign |
Het |
Map6 |
A |
G |
7: 98,985,740 (GRCm39) |
N751S |
possibly damaging |
Het |
Mgrn1 |
G |
A |
16: 4,750,084 (GRCm39) |
D494N |
probably benign |
Het |
Myh6 |
A |
G |
14: 55,184,631 (GRCm39) |
F1567L |
probably benign |
Het |
Myo9b |
T |
C |
8: 71,778,549 (GRCm39) |
V461A |
probably benign |
Het |
Ncan |
A |
T |
8: 70,567,861 (GRCm39) |
S84T |
probably damaging |
Het |
Or4c3 |
A |
T |
2: 89,851,871 (GRCm39) |
Y180N |
probably damaging |
Het |
Or4f4b |
A |
G |
2: 111,313,699 (GRCm39) |
|
probably null |
Het |
Or52n20 |
T |
A |
7: 104,319,925 (GRCm39) |
N5K |
probably damaging |
Het |
Or8g31-ps1 |
A |
T |
9: 39,276,130 (GRCm39) |
M92L |
probably benign |
Het |
Parp4 |
CTTCCTCCCCCTCCCCTTCTCTCTGCTGGCACCCATATTCCTCCCCCTCCCCTTCTCTCTGCTGGCACCCATCTTCCTCCCCCTCCCCTTCTCCCTGCTGGCACCCATATTCCTCCCCCTCCCC |
CTTCCTCCCCCTCCCCTTCTCTCTGCTGGCACCCATCTTCCTCCCCCTCCCCTTCTCCCTGCTGGCACCCATATTCCTCCCCCTCCCC |
14: 56,885,303 (GRCm39) |
|
probably benign |
Het |
Pld1 |
C |
A |
3: 28,141,435 (GRCm39) |
T666K |
probably damaging |
Het |
Pnpla6 |
A |
G |
8: 3,588,068 (GRCm39) |
Y1107C |
probably damaging |
Het |
Pramel7 |
A |
C |
2: 87,322,706 (GRCm39) |
N19K |
probably benign |
Het |
Prh1 |
C |
G |
6: 132,548,721 (GRCm39) |
P76R |
unknown |
Het |
Prkd2 |
T |
C |
7: 16,579,865 (GRCm39) |
V121A |
possibly damaging |
Het |
Ptprq |
G |
A |
10: 107,471,367 (GRCm39) |
Q1345* |
probably null |
Het |
Ryr3 |
T |
A |
2: 112,732,948 (GRCm39) |
T653S |
probably benign |
Het |
Sall2 |
G |
T |
14: 52,551,868 (GRCm39) |
Y442* |
probably null |
Het |
Slc23a2 |
A |
C |
2: 131,931,026 (GRCm39) |
F158V |
probably benign |
Het |
Smg1 |
C |
A |
7: 117,765,322 (GRCm39) |
R1954L |
unknown |
Het |
Snx31 |
G |
A |
15: 36,523,596 (GRCm39) |
T362I |
probably damaging |
Het |
Taf3 |
G |
T |
2: 9,956,901 (GRCm39) |
T422K |
probably damaging |
Het |
Tcfl5 |
T |
C |
2: 180,283,958 (GRCm39) |
D142G |
probably benign |
Het |
Tmx1 |
A |
G |
12: 70,507,325 (GRCm39) |
T188A |
probably damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,735,866 (GRCm39) |
|
probably null |
Het |
Trio |
A |
T |
15: 27,871,375 (GRCm39) |
C640S |
possibly damaging |
Het |
Ulk4 |
T |
G |
9: 121,084,190 (GRCm39) |
N427T |
probably damaging |
Het |
Vmn1r202 |
T |
C |
13: 22,685,872 (GRCm39) |
M182V |
probably benign |
Het |
Vmn1r214 |
C |
T |
13: 23,218,839 (GRCm39) |
A111V |
probably benign |
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 |
R5644:Nlrp9a
|
UTSW |
7 |
26,257,993 (GRCm39) |
missense |
possibly damaging |
0.51 |
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 |
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'- TAGGGTTAAGAAGTCCAACTAGCATAG -3'
(R):5'- TGACCATGAGAGGCAGTGTG -3'
Sequencing Primer
(F):5'- TCTTTAAGGCATGAGAGCTAAGC -3'
(R):5'- CCATGAGAGGCAGTGTGTACTCAC -3'
|
Posted On |
2019-06-26 |