Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030624J02Rik |
T |
A |
7: 118,791,448 (GRCm38) |
I455N |
probably damaging |
Het |
A2m |
T |
C |
6: 121,638,284 (GRCm38) |
M1T |
probably null |
Het |
Aatf |
T |
A |
11: 84,449,138 (GRCm38) |
D449V |
probably damaging |
Het |
Acbd3 |
T |
A |
1: 180,721,944 (GRCm38) |
|
probably benign |
Het |
BC005561 |
A |
G |
5: 104,522,240 (GRCm38) |
K1543E |
probably benign |
Het |
Bicc1 |
T |
A |
10: 70,953,484 (GRCm38) |
I366F |
possibly damaging |
Het |
Ccdc74a |
T |
C |
16: 17,649,749 (GRCm38) |
S184P |
possibly damaging |
Het |
Cntn4 |
T |
C |
6: 106,525,485 (GRCm38) |
V401A |
probably damaging |
Het |
Cux2 |
T |
C |
5: 121,873,753 (GRCm38) |
T540A |
probably damaging |
Het |
Disp2 |
G |
T |
2: 118,791,684 (GRCm38) |
E966* |
probably null |
Het |
Dpp7 |
A |
G |
2: 25,354,919 (GRCm38) |
Y209H |
probably benign |
Het |
Dstyk |
T |
A |
1: 132,449,487 (GRCm38) |
F277Y |
probably damaging |
Het |
Dtx1 |
A |
T |
5: 120,694,408 (GRCm38) |
|
probably null |
Het |
Ear-ps2 |
G |
A |
14: 44,047,060 (GRCm38) |
|
noncoding transcript |
Het |
Ednra |
T |
C |
8: 77,664,995 (GRCm38) |
H422R |
probably benign |
Het |
Erlec1 |
T |
A |
11: 30,952,640 (GRCm38) |
I67F |
probably benign |
Het |
Fam161b |
G |
A |
12: 84,348,558 (GRCm38) |
|
probably benign |
Het |
Gata5 |
A |
T |
2: 180,327,379 (GRCm38) |
C345* |
probably null |
Het |
Glmp |
T |
C |
3: 88,328,274 (GRCm38) |
V47A |
probably damaging |
Het |
Gm9762 |
T |
A |
3: 78,966,550 (GRCm38) |
|
noncoding transcript |
Het |
Gnas |
A |
T |
2: 174,298,080 (GRCm38) |
D14V |
probably damaging |
Het |
Gnl3 |
T |
C |
14: 31,017,329 (GRCm38) |
S53G |
probably damaging |
Het |
Grhl3 |
C |
T |
4: 135,548,466 (GRCm38) |
V527M |
probably damaging |
Het |
Hoxd10 |
T |
A |
2: 74,694,187 (GRCm38) |
L281* |
probably null |
Het |
Kif16b |
T |
G |
2: 142,690,694 (GRCm38) |
Y1175S |
probably benign |
Het |
Kif2b |
A |
G |
11: 91,576,846 (GRCm38) |
S204P |
probably benign |
Het |
Klhl40 |
T |
A |
9: 121,778,734 (GRCm38) |
I320N |
probably damaging |
Het |
Ksr2 |
G |
A |
5: 117,708,147 (GRCm38) |
R693Q |
probably damaging |
Het |
Mis12 |
A |
G |
11: 71,025,326 (GRCm38) |
K62E |
possibly damaging |
Het |
Mlc1 |
A |
G |
15: 88,974,777 (GRCm38) |
C102R |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,857,361 (GRCm38) |
I1348T |
unknown |
Het |
Myh7b |
A |
G |
2: 155,629,322 (GRCm38) |
E1130G |
probably damaging |
Het |
Nat8f4 |
T |
C |
6: 85,901,386 (GRCm38) |
T52A |
probably benign |
Het |
Nxpe2 |
C |
A |
9: 48,320,521 (GRCm38) |
V379L |
probably benign |
Het |
Olfr1231 |
C |
A |
2: 89,302,902 (GRCm38) |
S230I |
possibly damaging |
Het |
Olfr1231 |
T |
A |
2: 89,302,903 (GRCm38) |
S230C |
probably damaging |
Het |
Olfr1448 |
C |
T |
19: 12,919,934 (GRCm38) |
C125Y |
probably damaging |
Het |
Olfr1465 |
A |
T |
19: 13,313,717 (GRCm38) |
D189E |
probably benign |
Het |
Olfr288 |
G |
A |
15: 98,186,868 (GRCm38) |
R310W |
probably damaging |
Het |
Pcdhga7 |
A |
T |
18: 37,717,208 (GRCm38) |
Y756F |
probably damaging |
Het |
Pcsk6 |
T |
A |
7: 65,959,241 (GRCm38) |
Y284N |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,126,347 (GRCm38) |
V1367A |
possibly damaging |
Het |
Postn |
T |
A |
3: 54,375,071 (GRCm38) |
N484K |
probably damaging |
Het |
Prkd3 |
C |
T |
17: 78,961,171 (GRCm38) |
V572I |
probably benign |
Het |
Qser1 |
T |
C |
2: 104,787,183 (GRCm38) |
S1005G |
probably benign |
Het |
Radil |
G |
T |
5: 142,486,801 (GRCm38) |
D951E |
probably benign |
Het |
Sacs |
T |
C |
14: 61,212,747 (GRCm38) |
F4081L |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,315,085 (GRCm38) |
V11A |
possibly damaging |
Het |
Sgip1 |
T |
A |
4: 102,934,587 (GRCm38) |
F536I |
probably damaging |
Het |
Slc45a1 |
A |
G |
4: 150,638,284 (GRCm38) |
L381P |
probably damaging |
Het |
Smarcad1 |
C |
T |
6: 65,052,641 (GRCm38) |
P71L |
probably benign |
Het |
Spns1 |
T |
A |
7: 126,377,037 (GRCm38) |
D14V |
probably damaging |
Het |
Sv2c |
T |
A |
13: 95,986,018 (GRCm38) |
I417F |
possibly damaging |
Het |
Tas2r113 |
T |
A |
6: 132,893,516 (GRCm38) |
M169K |
probably benign |
Het |
Tgm1 |
A |
T |
14: 55,705,681 (GRCm38) |
N567K |
probably benign |
Het |
Tln2 |
C |
T |
9: 67,395,461 (GRCm38) |
R76Q |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,853,791 (GRCm38) |
V1340A |
probably benign |
Het |
Tspan18 |
A |
T |
2: 93,312,030 (GRCm38) |
|
probably null |
Het |
Txndc11 |
C |
T |
16: 11,084,314 (GRCm38) |
V679I |
probably damaging |
Het |
Usf1 |
G |
T |
1: 171,416,964 (GRCm38) |
G144V |
possibly damaging |
Het |
Vmn1r59 |
T |
C |
7: 5,454,452 (GRCm38) |
Y103C |
probably damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,741,826 (GRCm38) |
I713F |
probably damaging |
Het |
Vmn2r79 |
A |
T |
7: 87,037,960 (GRCm38) |
I850F |
probably damaging |
Het |
Wdr90 |
C |
T |
17: 25,855,363 (GRCm38) |
R676H |
probably benign |
Het |
Zfp867 |
G |
A |
11: 59,463,661 (GRCm38) |
R281W |
probably damaging |
Het |
Zfp939 |
T |
C |
7: 39,472,942 (GRCm38) |
|
noncoding transcript |
Het |
|
Other mutations in Ripk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01443:Ripk1
|
APN |
13 |
34,015,268 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01873:Ripk1
|
APN |
13 |
34,009,724 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02383:Ripk1
|
APN |
13 |
34,015,244 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02478:Ripk1
|
APN |
13 |
34,010,589 (GRCm38) |
missense |
probably damaging |
1.00 |
R0115:Ripk1
|
UTSW |
13 |
34,009,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R0481:Ripk1
|
UTSW |
13 |
34,009,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R0630:Ripk1
|
UTSW |
13 |
34,027,781 (GRCm38) |
missense |
probably damaging |
1.00 |
R1105:Ripk1
|
UTSW |
13 |
34,028,167 (GRCm38) |
missense |
probably benign |
|
R1528:Ripk1
|
UTSW |
13 |
34,028,147 (GRCm38) |
missense |
probably benign |
0.01 |
R1834:Ripk1
|
UTSW |
13 |
34,015,213 (GRCm38) |
missense |
probably benign |
0.00 |
R2294:Ripk1
|
UTSW |
13 |
34,017,008 (GRCm38) |
missense |
probably benign |
|
R2384:Ripk1
|
UTSW |
13 |
34,030,043 (GRCm38) |
missense |
probably benign |
0.03 |
R4510:Ripk1
|
UTSW |
13 |
34,026,748 (GRCm38) |
missense |
probably damaging |
1.00 |
R4511:Ripk1
|
UTSW |
13 |
34,026,748 (GRCm38) |
missense |
probably damaging |
1.00 |
R5078:Ripk1
|
UTSW |
13 |
34,017,099 (GRCm38) |
missense |
probably damaging |
1.00 |
R5153:Ripk1
|
UTSW |
13 |
34,013,296 (GRCm38) |
missense |
probably damaging |
1.00 |
R5974:Ripk1
|
UTSW |
13 |
34,030,101 (GRCm38) |
nonsense |
probably null |
|
R6189:Ripk1
|
UTSW |
13 |
34,032,501 (GRCm38) |
missense |
probably benign |
0.16 |
R6676:Ripk1
|
UTSW |
13 |
34,010,604 (GRCm38) |
missense |
probably damaging |
1.00 |
R6905:Ripk1
|
UTSW |
13 |
34,027,990 (GRCm38) |
missense |
probably benign |
|
R6997:Ripk1
|
UTSW |
13 |
34,017,117 (GRCm38) |
missense |
probably benign |
0.00 |
R7009:Ripk1
|
UTSW |
13 |
34,030,062 (GRCm38) |
missense |
probably damaging |
1.00 |
R7956:Ripk1
|
UTSW |
13 |
34,009,683 (GRCm38) |
missense |
probably benign |
0.02 |
R8497:Ripk1
|
UTSW |
13 |
34,027,951 (GRCm38) |
missense |
probably damaging |
0.98 |
R8680:Ripk1
|
UTSW |
13 |
34,030,049 (GRCm38) |
missense |
possibly damaging |
0.54 |
R9021:Ripk1
|
UTSW |
13 |
34,021,390 (GRCm38) |
missense |
probably benign |
0.38 |
R9132:Ripk1
|
UTSW |
13 |
34,028,201 (GRCm38) |
missense |
probably benign |
0.01 |
R9620:Ripk1
|
UTSW |
13 |
34,026,823 (GRCm38) |
missense |
possibly damaging |
0.91 |
Z1177:Ripk1
|
UTSW |
13 |
34,028,135 (GRCm38) |
missense |
probably benign |
0.01 |
|