Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530068E07Rik |
A |
G |
11: 52,294,193 (GRCm39) |
R145G |
probably damaging |
Het |
Akr1c21 |
T |
A |
13: 4,627,431 (GRCm39) |
M175K |
probably benign |
Het |
Apol7a |
C |
T |
15: 77,273,530 (GRCm39) |
A311T |
probably damaging |
Het |
Atxn10 |
G |
T |
15: 85,260,896 (GRCm39) |
E214* |
probably null |
Het |
Bmp2k |
C |
T |
5: 97,234,823 (GRCm39) |
Q749* |
probably null |
Het |
Ccdc141 |
G |
A |
2: 76,876,023 (GRCm39) |
A669V |
probably benign |
Het |
Cndp2 |
A |
C |
18: 84,689,036 (GRCm39) |
C249G |
probably benign |
Het |
Cnr1 |
A |
G |
4: 33,944,802 (GRCm39) |
I397V |
possibly damaging |
Het |
Col19a1 |
T |
C |
1: 24,345,331 (GRCm39) |
|
probably benign |
Het |
Dbn1 |
T |
C |
13: 55,630,117 (GRCm39) |
|
probably benign |
Het |
Dmgdh |
C |
T |
13: 93,845,803 (GRCm39) |
P486S |
probably damaging |
Het |
Dpys |
A |
G |
15: 39,656,702 (GRCm39) |
V455A |
possibly damaging |
Het |
Farp2 |
A |
G |
1: 93,546,702 (GRCm39) |
N907S |
probably benign |
Het |
Fndc3c1 |
C |
T |
X: 105,476,378 (GRCm39) |
E894K |
probably benign |
Het |
Gm6685 |
A |
T |
11: 28,289,473 (GRCm39) |
N114K |
probably damaging |
Het |
Golga3 |
A |
T |
5: 110,365,675 (GRCm39) |
|
probably null |
Het |
Grin2c |
A |
G |
11: 115,151,708 (GRCm39) |
L84P |
probably damaging |
Het |
Gucy2c |
A |
G |
6: 136,675,009 (GRCm39) |
F1001L |
probably benign |
Het |
Hcn4 |
A |
G |
9: 58,767,169 (GRCm39) |
H910R |
unknown |
Het |
Kdm4b |
T |
C |
17: 56,660,518 (GRCm39) |
|
probably benign |
Het |
Lrrfip2 |
A |
G |
9: 111,043,284 (GRCm39) |
T497A |
probably benign |
Het |
Man2c1 |
A |
G |
9: 57,048,884 (GRCm39) |
Y924C |
probably damaging |
Het |
Nkain2 |
T |
A |
10: 32,278,237 (GRCm39) |
T63S |
probably damaging |
Het |
Or52n3 |
T |
C |
7: 104,530,037 (GRCm39) |
V41A |
probably benign |
Het |
Or52n4 |
T |
A |
7: 104,294,136 (GRCm39) |
I146F |
possibly damaging |
Het |
Pitrm1 |
T |
A |
13: 6,623,078 (GRCm39) |
C780S |
probably damaging |
Het |
Plekha5 |
C |
T |
6: 140,516,042 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
C |
T |
2: 72,005,185 (GRCm39) |
R193* |
probably null |
Het |
Rbm20 |
A |
G |
19: 53,840,044 (GRCm39) |
E1011G |
possibly damaging |
Het |
Rfx3 |
A |
T |
19: 27,746,050 (GRCm39) |
D685E |
probably benign |
Het |
Ror1 |
T |
C |
4: 100,190,984 (GRCm39) |
S114P |
probably damaging |
Het |
Slc17a6 |
A |
G |
7: 51,318,863 (GRCm39) |
K502E |
probably benign |
Het |
Spink2 |
A |
T |
5: 77,359,174 (GRCm39) |
|
probably benign |
Het |
Sptb |
A |
T |
12: 76,659,921 (GRCm39) |
I993N |
possibly damaging |
Het |
Stxbp4 |
A |
G |
11: 90,512,475 (GRCm39) |
|
probably benign |
Het |
Tes |
A |
T |
6: 17,099,878 (GRCm39) |
Y291F |
probably damaging |
Het |
Tmtc4 |
G |
T |
14: 123,163,366 (GRCm39) |
|
probably benign |
Het |
Trpa1 |
T |
C |
1: 14,959,637 (GRCm39) |
E683G |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,521,455 (GRCm39) |
D171G |
probably benign |
Het |
Wbp11 |
A |
G |
6: 136,791,612 (GRCm39) |
|
probably benign |
Het |
Wfdc12 |
A |
G |
2: 164,031,581 (GRCm39) |
*86R |
probably null |
Het |
Zfp281 |
T |
C |
1: 136,553,853 (GRCm39) |
V277A |
probably damaging |
Het |
|
Other mutations in Nlrp1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00648:Nlrp1a
|
APN |
11 |
70,983,783 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00771:Nlrp1a
|
APN |
11 |
71,013,567 (GRCm39) |
nonsense |
probably null |
|
IGL01886:Nlrp1a
|
APN |
11 |
71,014,327 (GRCm39) |
missense |
probably benign |
|
IGL02221:Nlrp1a
|
APN |
11 |
71,013,944 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02291:Nlrp1a
|
APN |
11 |
71,013,415 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02375:Nlrp1a
|
APN |
11 |
71,004,339 (GRCm39) |
nonsense |
probably null |
|
IGL02408:Nlrp1a
|
APN |
11 |
71,013,456 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02516:Nlrp1a
|
APN |
11 |
71,005,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02583:Nlrp1a
|
APN |
11 |
71,014,227 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02622:Nlrp1a
|
APN |
11 |
71,013,826 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02642:Nlrp1a
|
APN |
11 |
71,014,358 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02823:Nlrp1a
|
APN |
11 |
70,983,249 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02859:Nlrp1a
|
APN |
11 |
70,996,912 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02997:Nlrp1a
|
APN |
11 |
71,014,491 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03342:Nlrp1a
|
APN |
11 |
71,013,617 (GRCm39) |
missense |
probably benign |
0.19 |
Ants
|
UTSW |
11 |
71,033,164 (GRCm39) |
missense |
probably benign |
0.01 |
dreary
|
UTSW |
11 |
71,004,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
picnic
|
UTSW |
11 |
71,013,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
seedless
|
UTSW |
11 |
71,014,378 (GRCm39) |
missense |
probably benign |
0.44 |
watermelon
|
UTSW |
11 |
71,013,531 (GRCm39) |
missense |
probably benign |
0.08 |
R0022:Nlrp1a
|
UTSW |
11 |
71,014,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R0345:Nlrp1a
|
UTSW |
11 |
71,014,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Nlrp1a
|
UTSW |
11 |
71,004,830 (GRCm39) |
intron |
probably benign |
|
R0364:Nlrp1a
|
UTSW |
11 |
71,004,830 (GRCm39) |
intron |
probably benign |
|
R0566:Nlrp1a
|
UTSW |
11 |
71,013,768 (GRCm39) |
missense |
probably benign |
0.00 |
R1177:Nlrp1a
|
UTSW |
11 |
70,998,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Nlrp1a
|
UTSW |
11 |
71,004,292 (GRCm39) |
critical splice donor site |
probably null |
|
R1263:Nlrp1a
|
UTSW |
11 |
70,987,948 (GRCm39) |
missense |
probably benign |
0.01 |
R1681:Nlrp1a
|
UTSW |
11 |
71,033,184 (GRCm39) |
missense |
unknown |
|
R1743:Nlrp1a
|
UTSW |
11 |
71,015,032 (GRCm39) |
missense |
probably benign |
0.04 |
R1826:Nlrp1a
|
UTSW |
11 |
70,998,806 (GRCm39) |
intron |
probably benign |
|
R1826:Nlrp1a
|
UTSW |
11 |
71,013,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1981:Nlrp1a
|
UTSW |
11 |
70,989,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Nlrp1a
|
UTSW |
11 |
71,015,046 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2116:Nlrp1a
|
UTSW |
11 |
71,005,326 (GRCm39) |
nonsense |
probably null |
|
R2134:Nlrp1a
|
UTSW |
11 |
71,015,014 (GRCm39) |
missense |
probably benign |
0.00 |
R2148:Nlrp1a
|
UTSW |
11 |
71,013,733 (GRCm39) |
nonsense |
probably null |
|
R2301:Nlrp1a
|
UTSW |
11 |
70,996,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3029:Nlrp1a
|
UTSW |
11 |
71,014,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3113:Nlrp1a
|
UTSW |
11 |
71,014,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Nlrp1a
|
UTSW |
11 |
71,013,529 (GRCm39) |
missense |
probably benign |
0.08 |
R3898:Nlrp1a
|
UTSW |
11 |
71,013,700 (GRCm39) |
missense |
probably benign |
0.00 |
R4254:Nlrp1a
|
UTSW |
11 |
71,013,854 (GRCm39) |
nonsense |
probably null |
|
R4397:Nlrp1a
|
UTSW |
11 |
70,988,030 (GRCm39) |
missense |
probably benign |
0.00 |
R4647:Nlrp1a
|
UTSW |
11 |
70,987,952 (GRCm39) |
splice site |
probably null |
|
R4740:Nlrp1a
|
UTSW |
11 |
71,004,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4965:Nlrp1a
|
UTSW |
11 |
70,983,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5009:Nlrp1a
|
UTSW |
11 |
71,013,531 (GRCm39) |
missense |
probably benign |
0.08 |
R5103:Nlrp1a
|
UTSW |
11 |
70,990,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R5355:Nlrp1a
|
UTSW |
11 |
71,015,077 (GRCm39) |
missense |
probably benign |
0.00 |
R5577:Nlrp1a
|
UTSW |
11 |
70,990,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Nlrp1a
|
UTSW |
11 |
70,990,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Nlrp1a
|
UTSW |
11 |
70,989,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Nlrp1a
|
UTSW |
11 |
71,013,846 (GRCm39) |
missense |
probably benign |
0.00 |
R6220:Nlrp1a
|
UTSW |
11 |
71,033,164 (GRCm39) |
missense |
probably benign |
0.01 |
R6564:Nlrp1a
|
UTSW |
11 |
71,014,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:Nlrp1a
|
UTSW |
11 |
70,996,899 (GRCm39) |
missense |
probably benign |
0.00 |
R6925:Nlrp1a
|
UTSW |
11 |
70,983,339 (GRCm39) |
missense |
probably null |
0.99 |
R7013:Nlrp1a
|
UTSW |
11 |
71,014,378 (GRCm39) |
missense |
probably benign |
0.44 |
R7155:Nlrp1a
|
UTSW |
11 |
71,014,905 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7214:Nlrp1a
|
UTSW |
11 |
71,014,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Nlrp1a
|
UTSW |
11 |
71,015,068 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Nlrp1a
|
UTSW |
11 |
71,014,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7404:Nlrp1a
|
UTSW |
11 |
70,987,919 (GRCm39) |
nonsense |
probably null |
|
R7409:Nlrp1a
|
UTSW |
11 |
71,013,634 (GRCm39) |
missense |
probably benign |
0.03 |
R7410:Nlrp1a
|
UTSW |
11 |
71,014,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7440:Nlrp1a
|
UTSW |
11 |
70,983,150 (GRCm39) |
missense |
probably damaging |
0.99 |
R7447:Nlrp1a
|
UTSW |
11 |
70,983,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Nlrp1a
|
UTSW |
11 |
70,998,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7569:Nlrp1a
|
UTSW |
11 |
70,999,869 (GRCm39) |
missense |
probably benign |
0.00 |
R7600:Nlrp1a
|
UTSW |
11 |
70,989,740 (GRCm39) |
missense |
probably damaging |
0.96 |
R7634:Nlrp1a
|
UTSW |
11 |
70,990,354 (GRCm39) |
missense |
probably benign |
0.19 |
R7734:Nlrp1a
|
UTSW |
11 |
70,998,826 (GRCm39) |
missense |
unknown |
|
R7747:Nlrp1a
|
UTSW |
11 |
71,014,234 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8471:Nlrp1a
|
UTSW |
11 |
71,013,885 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8482:Nlrp1a
|
UTSW |
11 |
70,999,901 (GRCm39) |
splice site |
probably null |
|
R9008:Nlrp1a
|
UTSW |
11 |
71,014,735 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9028:Nlrp1a
|
UTSW |
11 |
71,013,819 (GRCm39) |
missense |
probably benign |
0.27 |
R9441:Nlrp1a
|
UTSW |
11 |
71,013,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Nlrp1a
|
UTSW |
11 |
70,998,488 (GRCm39) |
missense |
probably benign |
0.05 |
R9701:Nlrp1a
|
UTSW |
11 |
70,987,946 (GRCm39) |
missense |
probably benign |
0.08 |
X0026:Nlrp1a
|
UTSW |
11 |
71,033,142 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Nlrp1a
|
UTSW |
11 |
71,013,995 (GRCm39) |
missense |
probably benign |
0.27 |
Z1186:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1186:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1186:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1186:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1186:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1187:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1187:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1188:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1188:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1189:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1189:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1190:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1190:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1191:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1191:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1192:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1192:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
|