Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd3 |
G |
T |
18: 10,704,605 (GRCm39) |
T151K |
possibly damaging |
Het |
Acsf2 |
C |
T |
11: 94,463,412 (GRCm39) |
W130* |
probably null |
Het |
Aldh16a1 |
G |
A |
7: 44,797,413 (GRCm39) |
R132* |
probably null |
Het |
Amer3 |
C |
T |
1: 34,628,043 (GRCm39) |
P761S |
probably benign |
Het |
Amotl1 |
G |
T |
9: 14,459,969 (GRCm39) |
D886E |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 136,035,909 (GRCm39) |
F1383S |
probably damaging |
Het |
Col14a1 |
T |
A |
15: 55,225,781 (GRCm39) |
V148E |
unknown |
Het |
Col9a2 |
T |
A |
4: 120,910,403 (GRCm39) |
|
probably null |
Het |
Cyp2a5 |
T |
A |
7: 26,536,636 (GRCm39) |
M205K |
possibly damaging |
Het |
Dcst2 |
A |
T |
3: 89,277,825 (GRCm39) |
Q466L |
possibly damaging |
Het |
Ecel1 |
T |
C |
1: 87,080,853 (GRCm39) |
I350V |
possibly damaging |
Het |
Enthd1 |
G |
A |
15: 80,336,901 (GRCm39) |
T511I |
probably benign |
Het |
Exoc6b |
T |
A |
6: 84,988,302 (GRCm39) |
K92* |
probably null |
Het |
Fam181a |
T |
G |
12: 103,282,591 (GRCm39) |
Y165* |
probably null |
Het |
Fbxo34 |
A |
G |
14: 47,768,725 (GRCm39) |
Y746C |
probably damaging |
Het |
Fgfr4 |
T |
A |
13: 55,308,994 (GRCm39) |
S372T |
possibly damaging |
Het |
Fmo1 |
A |
G |
1: 162,661,390 (GRCm39) |
F298L |
probably benign |
Het |
Gad1 |
A |
C |
2: 70,404,620 (GRCm39) |
D170A |
possibly damaging |
Het |
Garin2 |
A |
C |
12: 78,762,077 (GRCm39) |
D247A |
probably damaging |
Het |
Golgb1 |
T |
C |
16: 36,739,811 (GRCm39) |
S2758P |
probably benign |
Het |
Golm2 |
T |
C |
2: 121,737,242 (GRCm39) |
V261A |
probably benign |
Het |
H2az2 |
A |
T |
11: 6,379,094 (GRCm39) |
|
probably null |
Het |
Ilkap |
A |
G |
1: 91,303,973 (GRCm39) |
C163R |
|
Het |
Krt9 |
A |
T |
11: 100,079,186 (GRCm39) |
D735E |
unknown |
Het |
Lipo3 |
A |
T |
19: 33,559,629 (GRCm39) |
C80* |
probably null |
Het |
Lpcat3 |
C |
T |
6: 124,680,543 (GRCm39) |
P478L |
probably damaging |
Het |
Luc7l3 |
G |
A |
11: 94,212,545 (GRCm39) |
R24C |
unknown |
Het |
Mafa |
T |
A |
15: 75,619,161 (GRCm39) |
H204L |
probably benign |
Het |
Mapk10 |
A |
C |
5: 103,114,473 (GRCm39) |
V305G |
probably damaging |
Het |
Mgat1 |
T |
C |
11: 49,152,122 (GRCm39) |
F202L |
probably benign |
Het |
Mical2 |
A |
T |
7: 111,980,403 (GRCm39) |
T126S |
probably benign |
Het |
Mill1 |
G |
A |
7: 17,997,027 (GRCm39) |
R206H |
probably benign |
Het |
Nlrc5 |
A |
T |
8: 95,203,034 (GRCm39) |
Y378F |
probably benign |
Het |
Nlrp9a |
G |
T |
7: 26,250,469 (GRCm39) |
R78L |
probably damaging |
Het |
Or10b1 |
G |
T |
10: 78,356,128 (GRCm39) |
A229S |
probably benign |
Het |
Or52i2 |
A |
T |
7: 102,320,011 (GRCm39) |
I295F |
possibly damaging |
Het |
Or8g50 |
A |
T |
9: 39,648,287 (GRCm39) |
M59L |
|
Het |
Orc6 |
A |
T |
8: 86,026,430 (GRCm39) |
|
probably benign |
Het |
Pate14 |
A |
G |
9: 36,548,498 (GRCm39) |
|
probably null |
Het |
Pcdhgb5 |
C |
T |
18: 37,864,486 (GRCm39) |
Q94* |
probably null |
Het |
Pcnx1 |
A |
G |
12: 81,996,960 (GRCm39) |
D952G |
probably damaging |
Het |
Ppfia2 |
A |
T |
10: 106,749,519 (GRCm39) |
H1135L |
|
Het |
Prmt2 |
A |
T |
10: 76,061,213 (GRCm39) |
I91N |
probably damaging |
Het |
Ptprm |
A |
G |
17: 67,116,484 (GRCm39) |
Y932H |
probably damaging |
Het |
Qrich2 |
T |
C |
11: 116,337,946 (GRCm39) |
K154R |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 72,036,051 (GRCm39) |
T515A |
probably benign |
Het |
Rgmb |
G |
A |
17: 16,041,279 (GRCm39) |
R103* |
probably null |
Het |
Rnf5 |
C |
T |
17: 34,820,721 (GRCm39) |
G147S |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,715,138 (GRCm39) |
Y4662C |
unknown |
Het |
Secisbp2l |
A |
G |
2: 125,589,394 (GRCm39) |
M718T |
probably damaging |
Het |
Slc16a6 |
T |
C |
11: 109,354,322 (GRCm39) |
T100A |
probably benign |
Het |
Slc27a6 |
T |
A |
18: 58,742,887 (GRCm39) |
M525K |
probably damaging |
Het |
Slco2a1 |
G |
C |
9: 102,962,065 (GRCm39) |
C579S |
probably damaging |
Het |
Snx14 |
A |
G |
9: 88,263,794 (GRCm39) |
S864P |
probably damaging |
Het |
Spata31f3 |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
4: 42,871,823 (GRCm39) |
|
probably benign |
Het |
Sptbn2 |
T |
C |
19: 4,800,535 (GRCm39) |
L2250P |
probably damaging |
Het |
Tlr6 |
A |
T |
5: 65,112,146 (GRCm39) |
S254T |
possibly damaging |
Het |
Trap1 |
A |
T |
16: 3,858,083 (GRCm39) |
Y675* |
probably null |
Het |
Ttc9b |
C |
A |
7: 27,353,512 (GRCm39) |
A54E |
probably damaging |
Het |
Unc45a |
A |
C |
7: 79,975,403 (GRCm39) |
Y934D |
probably damaging |
Het |
Usp17ld |
A |
G |
7: 102,900,179 (GRCm39) |
L251P |
possibly damaging |
Het |
Usp42 |
A |
G |
5: 143,703,154 (GRCm39) |
V489A |
probably damaging |
Het |
Vars1 |
A |
G |
17: 35,235,001 (GRCm39) |
T1277A |
unknown |
Het |
Vmn2r117 |
A |
G |
17: 23,697,450 (GRCm39) |
S81P |
probably damaging |
Het |
Vmn2r69 |
T |
A |
7: 85,061,504 (GRCm39) |
I157F |
probably benign |
Het |
Zfp697 |
A |
G |
3: 98,335,182 (GRCm39) |
S316G |
probably damaging |
Het |
Zfp729b |
T |
A |
13: 67,739,787 (GRCm39) |
H826L |
probably damaging |
Het |
|
Other mutations in Ripk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01443:Ripk1
|
APN |
13 |
34,199,251 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01873:Ripk1
|
APN |
13 |
34,193,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:Ripk1
|
APN |
13 |
34,199,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02478:Ripk1
|
APN |
13 |
34,194,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Ripk1
|
UTSW |
13 |
34,193,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Ripk1
|
UTSW |
13 |
34,193,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Ripk1
|
UTSW |
13 |
34,211,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R1105:Ripk1
|
UTSW |
13 |
34,212,150 (GRCm39) |
missense |
probably benign |
|
R1528:Ripk1
|
UTSW |
13 |
34,212,130 (GRCm39) |
missense |
probably benign |
0.01 |
R1834:Ripk1
|
UTSW |
13 |
34,199,196 (GRCm39) |
missense |
probably benign |
0.00 |
R2294:Ripk1
|
UTSW |
13 |
34,200,991 (GRCm39) |
missense |
probably benign |
|
R2384:Ripk1
|
UTSW |
13 |
34,214,026 (GRCm39) |
missense |
probably benign |
0.03 |
R4510:Ripk1
|
UTSW |
13 |
34,210,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R4511:Ripk1
|
UTSW |
13 |
34,210,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Ripk1
|
UTSW |
13 |
34,211,925 (GRCm39) |
nonsense |
probably null |
|
R5078:Ripk1
|
UTSW |
13 |
34,201,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Ripk1
|
UTSW |
13 |
34,197,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Ripk1
|
UTSW |
13 |
34,214,084 (GRCm39) |
nonsense |
probably null |
|
R6189:Ripk1
|
UTSW |
13 |
34,216,484 (GRCm39) |
missense |
probably benign |
0.16 |
R6676:Ripk1
|
UTSW |
13 |
34,194,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R6905:Ripk1
|
UTSW |
13 |
34,211,973 (GRCm39) |
missense |
probably benign |
|
R6997:Ripk1
|
UTSW |
13 |
34,201,100 (GRCm39) |
missense |
probably benign |
0.00 |
R7009:Ripk1
|
UTSW |
13 |
34,214,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7956:Ripk1
|
UTSW |
13 |
34,193,666 (GRCm39) |
missense |
probably benign |
0.02 |
R8497:Ripk1
|
UTSW |
13 |
34,211,934 (GRCm39) |
missense |
probably damaging |
0.98 |
R8680:Ripk1
|
UTSW |
13 |
34,214,032 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9021:Ripk1
|
UTSW |
13 |
34,205,373 (GRCm39) |
missense |
probably benign |
0.38 |
R9132:Ripk1
|
UTSW |
13 |
34,212,184 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Ripk1
|
UTSW |
13 |
34,212,118 (GRCm39) |
missense |
probably benign |
0.01 |
|