Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
A |
T |
14: 29,708,298 (GRCm39) |
N192I |
probably damaging |
Het |
Arhgap15 |
A |
T |
2: 43,953,849 (GRCm39) |
I192F |
probably damaging |
Het |
Atp10a |
T |
C |
7: 58,463,379 (GRCm39) |
F971L |
probably benign |
Het |
Cacna1e |
G |
T |
1: 154,302,274 (GRCm39) |
F1660L |
probably damaging |
Het |
Cep152 |
G |
A |
2: 125,421,469 (GRCm39) |
T1087M |
probably damaging |
Het |
Ces2b |
T |
C |
8: 105,559,202 (GRCm39) |
|
probably benign |
Het |
Col19a1 |
T |
C |
1: 24,573,115 (GRCm39) |
D219G |
unknown |
Het |
Desi2 |
G |
A |
1: 178,076,843 (GRCm39) |
A116T |
probably damaging |
Het |
Eri2 |
T |
A |
7: 119,386,665 (GRCm39) |
Q202L |
probably damaging |
Het |
Gtf2ird1 |
G |
A |
5: 134,405,895 (GRCm39) |
P715L |
probably damaging |
Het |
Higd1c |
A |
T |
15: 100,281,622 (GRCm39) |
M249L |
probably benign |
Het |
Il5ra |
T |
A |
6: 106,719,644 (GRCm39) |
H63L |
possibly damaging |
Het |
Lamb3 |
T |
A |
1: 193,014,469 (GRCm39) |
C543S |
probably damaging |
Het |
Lnpep |
T |
A |
17: 17,791,162 (GRCm39) |
I461F |
possibly damaging |
Het |
Lum |
A |
G |
10: 97,404,609 (GRCm39) |
H168R |
probably benign |
Het |
Magi1 |
T |
C |
6: 93,762,591 (GRCm39) |
E77G |
possibly damaging |
Het |
Mrpl13 |
T |
C |
15: 55,421,135 (GRCm39) |
|
probably null |
Het |
Mtpap |
T |
A |
18: 4,380,703 (GRCm39) |
L127* |
probably null |
Het |
Myo15a |
T |
C |
11: 60,382,609 (GRCm39) |
|
probably benign |
Het |
Nek1 |
A |
G |
8: 61,542,514 (GRCm39) |
S726G |
probably benign |
Het |
Nynrin |
G |
A |
14: 56,103,554 (GRCm39) |
|
probably benign |
Het |
Or14c40 |
A |
G |
7: 86,313,289 (GRCm39) |
M140V |
probably benign |
Het |
Or2h15 |
C |
T |
17: 38,441,427 (GRCm39) |
G219S |
possibly damaging |
Het |
Pappa2 |
A |
T |
1: 158,764,364 (GRCm39) |
D382E |
probably damaging |
Het |
Plekhg1 |
T |
A |
10: 3,907,069 (GRCm39) |
L516* |
probably null |
Het |
Prune1 |
A |
G |
3: 95,162,711 (GRCm39) |
S321P |
possibly damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Syncrip |
G |
T |
9: 88,338,457 (GRCm39) |
R536S |
probably benign |
Het |
Thbs1 |
T |
G |
2: 117,945,273 (GRCm39) |
V282G |
probably benign |
Het |
Unc13b |
C |
T |
4: 43,235,332 (GRCm39) |
R880C |
probably damaging |
Het |
Vmn2r77 |
T |
G |
7: 86,449,979 (GRCm39) |
I75S |
probably benign |
Het |
Vps13a |
A |
T |
19: 16,630,063 (GRCm39) |
I2690K |
probably damaging |
Het |
Zfp286 |
T |
C |
11: 62,674,563 (GRCm39) |
N94S |
possibly damaging |
Het |
|
Other mutations in Nlrp5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00478:Nlrp5
|
APN |
7 |
23,141,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01393:Nlrp5
|
APN |
7 |
23,103,599 (GRCm39) |
missense |
probably null |
0.04 |
IGL01505:Nlrp5
|
APN |
7 |
23,117,159 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02010:Nlrp5
|
APN |
7 |
23,116,797 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02223:Nlrp5
|
APN |
7 |
23,129,447 (GRCm39) |
splice site |
probably benign |
|
IGL02341:Nlrp5
|
APN |
7 |
23,103,577 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02532:Nlrp5
|
APN |
7 |
23,109,398 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02619:Nlrp5
|
APN |
7 |
23,123,489 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02828:Nlrp5
|
APN |
7 |
23,120,885 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03018:Nlrp5
|
APN |
7 |
23,117,172 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03164:Nlrp5
|
APN |
7 |
23,117,798 (GRCm39) |
nonsense |
probably null |
|
IGL03397:Nlrp5
|
APN |
7 |
23,112,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03404:Nlrp5
|
APN |
7 |
23,129,459 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Nlrp5
|
UTSW |
7 |
23,129,582 (GRCm39) |
missense |
probably damaging |
0.99 |
R0549:Nlrp5
|
UTSW |
7 |
23,141,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Nlrp5
|
UTSW |
7 |
23,117,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0647:Nlrp5
|
UTSW |
7 |
23,117,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Nlrp5
|
UTSW |
7 |
23,116,842 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0826:Nlrp5
|
UTSW |
7 |
23,117,133 (GRCm39) |
missense |
probably benign |
0.13 |
R1511:Nlrp5
|
UTSW |
7 |
23,112,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R1620:Nlrp5
|
UTSW |
7 |
23,118,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Nlrp5
|
UTSW |
7 |
23,117,586 (GRCm39) |
missense |
probably damaging |
0.98 |
R1867:Nlrp5
|
UTSW |
7 |
23,123,407 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1887:Nlrp5
|
UTSW |
7 |
23,116,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Nlrp5
|
UTSW |
7 |
23,104,222 (GRCm39) |
missense |
probably benign |
0.00 |
R1901:Nlrp5
|
UTSW |
7 |
23,123,335 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2032:Nlrp5
|
UTSW |
7 |
23,120,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R3083:Nlrp5
|
UTSW |
7 |
23,129,588 (GRCm39) |
missense |
probably benign |
0.03 |
R3806:Nlrp5
|
UTSW |
7 |
23,104,271 (GRCm39) |
missense |
probably benign |
|
R3907:Nlrp5
|
UTSW |
7 |
23,133,071 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4085:Nlrp5
|
UTSW |
7 |
23,129,523 (GRCm39) |
missense |
probably damaging |
0.97 |
R4135:Nlrp5
|
UTSW |
7 |
23,117,823 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4609:Nlrp5
|
UTSW |
7 |
23,117,173 (GRCm39) |
missense |
probably benign |
0.01 |
R4649:Nlrp5
|
UTSW |
7 |
23,117,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R4780:Nlrp5
|
UTSW |
7 |
23,135,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Nlrp5
|
UTSW |
7 |
23,117,055 (GRCm39) |
missense |
probably damaging |
0.97 |
R5062:Nlrp5
|
UTSW |
7 |
23,135,335 (GRCm39) |
nonsense |
probably null |
|
R5224:Nlrp5
|
UTSW |
7 |
23,117,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:Nlrp5
|
UTSW |
7 |
23,117,753 (GRCm39) |
nonsense |
probably null |
|
R5426:Nlrp5
|
UTSW |
7 |
23,117,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R5488:Nlrp5
|
UTSW |
7 |
23,117,359 (GRCm39) |
missense |
probably benign |
0.03 |
R5762:Nlrp5
|
UTSW |
7 |
23,118,264 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6014:Nlrp5
|
UTSW |
7 |
23,109,372 (GRCm39) |
missense |
probably benign |
0.02 |
R6130:Nlrp5
|
UTSW |
7 |
23,103,598 (GRCm39) |
missense |
probably benign |
0.00 |
R6277:Nlrp5
|
UTSW |
7 |
23,120,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R6509:Nlrp5
|
UTSW |
7 |
23,117,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:Nlrp5
|
UTSW |
7 |
23,117,343 (GRCm39) |
missense |
probably benign |
0.22 |
R7042:Nlrp5
|
UTSW |
7 |
23,116,905 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7253:Nlrp5
|
UTSW |
7 |
23,116,816 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7336:Nlrp5
|
UTSW |
7 |
23,117,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R7371:Nlrp5
|
UTSW |
7 |
23,117,848 (GRCm39) |
missense |
probably damaging |
0.99 |
R7449:Nlrp5
|
UTSW |
7 |
23,116,951 (GRCm39) |
missense |
probably benign |
0.00 |
R7505:Nlrp5
|
UTSW |
7 |
23,106,925 (GRCm39) |
missense |
probably benign |
0.01 |
R7580:Nlrp5
|
UTSW |
7 |
23,133,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7588:Nlrp5
|
UTSW |
7 |
23,107,576 (GRCm39) |
missense |
probably benign |
0.21 |
R7793:Nlrp5
|
UTSW |
7 |
23,123,343 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7795:Nlrp5
|
UTSW |
7 |
23,118,219 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7893:Nlrp5
|
UTSW |
7 |
23,117,590 (GRCm39) |
missense |
probably benign |
0.12 |
R8071:Nlrp5
|
UTSW |
7 |
23,117,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8170:Nlrp5
|
UTSW |
7 |
23,133,135 (GRCm39) |
missense |
probably benign |
0.17 |
R8195:Nlrp5
|
UTSW |
7 |
23,112,762 (GRCm39) |
missense |
probably benign |
0.00 |
R8212:Nlrp5
|
UTSW |
7 |
23,116,762 (GRCm39) |
missense |
probably benign |
0.02 |
R8232:Nlrp5
|
UTSW |
7 |
23,116,770 (GRCm39) |
missense |
probably benign |
0.00 |
R8743:Nlrp5
|
UTSW |
7 |
23,118,172 (GRCm39) |
missense |
probably benign |
0.28 |
R8853:Nlrp5
|
UTSW |
7 |
23,117,725 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9030:Nlrp5
|
UTSW |
7 |
23,129,573 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9225:Nlrp5
|
UTSW |
7 |
23,117,371 (GRCm39) |
missense |
probably benign |
0.24 |
R9463:Nlrp5
|
UTSW |
7 |
23,118,225 (GRCm39) |
missense |
probably benign |
0.24 |
R9615:Nlrp5
|
UTSW |
7 |
23,107,561 (GRCm39) |
missense |
probably benign |
0.10 |
R9647:Nlrp5
|
UTSW |
7 |
23,107,576 (GRCm39) |
missense |
probably benign |
0.12 |
R9664:Nlrp5
|
UTSW |
7 |
23,118,286 (GRCm39) |
missense |
probably benign |
0.01 |
R9744:Nlrp5
|
UTSW |
7 |
23,120,902 (GRCm39) |
missense |
possibly damaging |
0.80 |
RF007:Nlrp5
|
UTSW |
7 |
23,117,586 (GRCm39) |
missense |
probably benign |
0.16 |
U24488:Nlrp5
|
UTSW |
7 |
23,117,653 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0026:Nlrp5
|
UTSW |
7 |
23,116,923 (GRCm39) |
nonsense |
probably null |
|
X0062:Nlrp5
|
UTSW |
7 |
23,117,415 (GRCm39) |
nonsense |
probably null |
|
Z1088:Nlrp5
|
UTSW |
7 |
23,117,011 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Nlrp5
|
UTSW |
7 |
23,103,592 (GRCm39) |
missense |
possibly damaging |
0.82 |
|