Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ache |
A |
G |
5: 137,289,371 (GRCm39) |
|
probably benign |
Het |
Atr |
A |
T |
9: 95,744,905 (GRCm39) |
H74L |
probably damaging |
Het |
Brca2 |
A |
T |
5: 150,465,255 (GRCm39) |
H1673L |
possibly damaging |
Het |
Brwd1 |
A |
T |
16: 95,853,771 (GRCm39) |
I495K |
probably damaging |
Het |
Cacna1s |
A |
T |
1: 135,998,743 (GRCm39) |
I213F |
probably benign |
Het |
Cds1 |
T |
C |
5: 101,962,332 (GRCm39) |
S316P |
possibly damaging |
Het |
Ces1b |
G |
A |
8: 93,806,038 (GRCm39) |
P68S |
probably damaging |
Het |
Cilp |
A |
G |
9: 65,185,206 (GRCm39) |
I434V |
probably benign |
Het |
Csgalnact2 |
A |
G |
6: 118,106,229 (GRCm39) |
Y30H |
probably damaging |
Het |
Defb7 |
T |
C |
8: 19,545,140 (GRCm39) |
V6A |
probably benign |
Het |
Dlg2 |
A |
T |
7: 92,080,335 (GRCm39) |
L841F |
probably damaging |
Het |
Dnajc14 |
A |
G |
10: 128,642,468 (GRCm39) |
N130S |
possibly damaging |
Het |
Dock7 |
T |
A |
4: 98,833,732 (GRCm39) |
D1863V |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,376,897 (GRCm39) |
R1561G |
possibly damaging |
Het |
Fads2b |
G |
T |
2: 85,332,551 (GRCm39) |
R158S |
possibly damaging |
Het |
Gstt4 |
G |
T |
10: 75,658,174 (GRCm39) |
F28L |
probably damaging |
Het |
Hectd1 |
G |
T |
12: 51,810,864 (GRCm39) |
D1690E |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,282,441 (GRCm39) |
S3394P |
probably benign |
Het |
Ift25 |
T |
C |
4: 107,132,492 (GRCm39) |
|
probably benign |
Het |
Igf2r |
A |
T |
17: 12,911,610 (GRCm39) |
C1910S |
probably damaging |
Het |
Jakmip2 |
T |
C |
18: 43,708,516 (GRCm39) |
|
probably benign |
Het |
Kif1b |
C |
T |
4: 149,330,821 (GRCm39) |
V612M |
probably damaging |
Het |
Lrrd1 |
A |
G |
5: 3,900,709 (GRCm39) |
E338G |
probably damaging |
Het |
Mmp9 |
C |
A |
2: 164,791,723 (GRCm39) |
D205E |
probably damaging |
Het |
Mylk |
A |
T |
16: 34,735,270 (GRCm39) |
H750L |
probably benign |
Het |
Naip6 |
A |
G |
13: 100,436,121 (GRCm39) |
S801P |
probably damaging |
Het |
Nlrp1b |
A |
T |
11: 71,051,998 (GRCm39) |
M980K |
probably benign |
Het |
Or14j1 |
G |
A |
17: 38,146,831 (GRCm39) |
V314I |
probably benign |
Het |
Or2y3 |
T |
C |
17: 38,393,243 (GRCm39) |
K209E |
possibly damaging |
Het |
Or5d43 |
C |
A |
2: 88,104,776 (GRCm39) |
V206F |
probably benign |
Het |
Or6c88 |
A |
G |
10: 129,406,619 (GRCm39) |
T32A |
probably benign |
Het |
Pdk1 |
A |
G |
2: 71,727,989 (GRCm39) |
|
probably null |
Het |
Pex7 |
A |
G |
10: 19,770,500 (GRCm39) |
S125P |
probably damaging |
Het |
Pigu |
T |
C |
2: 155,187,565 (GRCm39) |
|
probably benign |
Het |
Prr16 |
T |
A |
18: 51,436,164 (GRCm39) |
H214Q |
probably damaging |
Het |
Psme4 |
C |
T |
11: 30,800,715 (GRCm39) |
|
probably benign |
Het |
Sf3b3 |
A |
G |
8: 111,538,609 (GRCm39) |
|
probably null |
Het |
Sp4 |
T |
C |
12: 118,225,616 (GRCm39) |
I583V |
probably benign |
Het |
Spata22 |
A |
G |
11: 73,234,569 (GRCm39) |
T224A |
probably benign |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tmem119 |
T |
A |
5: 113,933,432 (GRCm39) |
Y123F |
probably damaging |
Het |
Umps |
A |
T |
16: 33,782,523 (GRCm39) |
L133* |
probably null |
Het |
Usp46 |
T |
A |
5: 74,177,343 (GRCm39) |
T179S |
probably benign |
Het |
Vtcn1 |
T |
A |
3: 100,795,701 (GRCm39) |
Y223N |
probably damaging |
Het |
Wiz |
A |
G |
17: 32,576,853 (GRCm39) |
M567T |
probably damaging |
Het |
|
Other mutations in Katnip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00697:Katnip
|
APN |
7 |
125,394,622 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL00950:Katnip
|
APN |
7 |
125,442,393 (GRCm39) |
missense |
probably benign |
|
IGL01089:Katnip
|
APN |
7 |
125,394,485 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:Katnip
|
APN |
7 |
125,464,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01449:Katnip
|
APN |
7 |
125,469,857 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01545:Katnip
|
APN |
7 |
125,352,143 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01937:Katnip
|
APN |
7 |
125,453,777 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01949:Katnip
|
APN |
7 |
125,361,014 (GRCm39) |
nonsense |
probably null |
|
IGL02096:Katnip
|
APN |
7 |
125,413,993 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02148:Katnip
|
APN |
7 |
125,472,648 (GRCm39) |
splice site |
probably null |
|
IGL02274:Katnip
|
APN |
7 |
125,369,742 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02323:Katnip
|
APN |
7 |
125,442,001 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02574:Katnip
|
APN |
7 |
125,428,925 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02639:Katnip
|
APN |
7 |
125,471,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03003:Katnip
|
APN |
7 |
125,451,132 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03011:Katnip
|
APN |
7 |
125,451,174 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03332:Katnip
|
APN |
7 |
125,419,277 (GRCm39) |
nonsense |
probably null |
|
IGL03368:Katnip
|
APN |
7 |
125,468,030 (GRCm39) |
intron |
probably benign |
|
E0370:Katnip
|
UTSW |
7 |
125,449,474 (GRCm39) |
missense |
probably benign |
0.06 |
PIT4498001:Katnip
|
UTSW |
7 |
125,412,768 (GRCm39) |
missense |
probably benign |
|
R0033:Katnip
|
UTSW |
7 |
125,360,999 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0033:Katnip
|
UTSW |
7 |
125,360,999 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0234:Katnip
|
UTSW |
7 |
125,394,557 (GRCm39) |
missense |
probably benign |
0.00 |
R0234:Katnip
|
UTSW |
7 |
125,394,557 (GRCm39) |
missense |
probably benign |
0.00 |
R0472:Katnip
|
UTSW |
7 |
125,472,139 (GRCm39) |
missense |
probably damaging |
0.98 |
R0479:Katnip
|
UTSW |
7 |
125,442,518 (GRCm39) |
missense |
probably benign |
0.20 |
R1195:Katnip
|
UTSW |
7 |
125,465,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Katnip
|
UTSW |
7 |
125,465,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Katnip
|
UTSW |
7 |
125,465,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Katnip
|
UTSW |
7 |
125,359,595 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1299:Katnip
|
UTSW |
7 |
125,451,195 (GRCm39) |
missense |
probably benign |
|
R1331:Katnip
|
UTSW |
7 |
125,465,627 (GRCm39) |
missense |
probably benign |
0.00 |
R1484:Katnip
|
UTSW |
7 |
125,415,743 (GRCm39) |
splice site |
probably benign |
|
R1507:Katnip
|
UTSW |
7 |
125,465,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Katnip
|
UTSW |
7 |
125,442,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Katnip
|
UTSW |
7 |
125,419,261 (GRCm39) |
missense |
probably benign |
0.00 |
R2008:Katnip
|
UTSW |
7 |
125,459,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Katnip
|
UTSW |
7 |
125,472,128 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2147:Katnip
|
UTSW |
7 |
125,464,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Katnip
|
UTSW |
7 |
125,394,515 (GRCm39) |
missense |
probably benign |
|
R3015:Katnip
|
UTSW |
7 |
125,465,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R3794:Katnip
|
UTSW |
7 |
125,419,261 (GRCm39) |
missense |
probably benign |
0.00 |
R3795:Katnip
|
UTSW |
7 |
125,419,261 (GRCm39) |
missense |
probably benign |
0.00 |
R4043:Katnip
|
UTSW |
7 |
125,467,913 (GRCm39) |
missense |
probably benign |
0.30 |
R4044:Katnip
|
UTSW |
7 |
125,467,913 (GRCm39) |
missense |
probably benign |
0.30 |
R4692:Katnip
|
UTSW |
7 |
125,466,841 (GRCm39) |
critical splice donor site |
probably null |
|
R4772:Katnip
|
UTSW |
7 |
125,464,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R5155:Katnip
|
UTSW |
7 |
125,471,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R5467:Katnip
|
UTSW |
7 |
125,442,527 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5551:Katnip
|
UTSW |
7 |
125,419,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Katnip
|
UTSW |
7 |
125,453,733 (GRCm39) |
missense |
probably benign |
0.00 |
R5662:Katnip
|
UTSW |
7 |
125,441,875 (GRCm39) |
missense |
probably benign |
0.00 |
R5667:Katnip
|
UTSW |
7 |
125,442,627 (GRCm39) |
critical splice donor site |
probably null |
|
R5838:Katnip
|
UTSW |
7 |
125,466,827 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5958:Katnip
|
UTSW |
7 |
125,412,807 (GRCm39) |
missense |
probably benign |
0.01 |
R5983:Katnip
|
UTSW |
7 |
125,449,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R6084:Katnip
|
UTSW |
7 |
125,414,037 (GRCm39) |
missense |
probably benign |
|
R6241:Katnip
|
UTSW |
7 |
125,472,006 (GRCm39) |
missense |
probably benign |
0.00 |
R6298:Katnip
|
UTSW |
7 |
125,469,869 (GRCm39) |
missense |
probably benign |
0.11 |
R6345:Katnip
|
UTSW |
7 |
125,352,159 (GRCm39) |
missense |
probably damaging |
0.97 |
R6554:Katnip
|
UTSW |
7 |
125,449,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6715:Katnip
|
UTSW |
7 |
125,361,001 (GRCm39) |
nonsense |
probably null |
|
R6745:Katnip
|
UTSW |
7 |
125,369,822 (GRCm39) |
missense |
probably benign |
0.00 |
R7178:Katnip
|
UTSW |
7 |
125,465,499 (GRCm39) |
missense |
probably benign |
0.00 |
R7210:Katnip
|
UTSW |
7 |
125,471,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R7404:Katnip
|
UTSW |
7 |
125,464,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R7561:Katnip
|
UTSW |
7 |
125,441,894 (GRCm39) |
missense |
probably benign |
|
R7571:Katnip
|
UTSW |
7 |
125,307,193 (GRCm39) |
unclassified |
probably benign |
|
R7584:Katnip
|
UTSW |
7 |
125,469,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R7629:Katnip
|
UTSW |
7 |
125,394,422 (GRCm39) |
missense |
probably damaging |
0.96 |
R7676:Katnip
|
UTSW |
7 |
125,449,549 (GRCm39) |
missense |
probably benign |
0.26 |
R7748:Katnip
|
UTSW |
7 |
125,428,973 (GRCm39) |
missense |
probably benign |
0.00 |
R7786:Katnip
|
UTSW |
7 |
125,464,466 (GRCm39) |
missense |
probably benign |
0.19 |
R8058:Katnip
|
UTSW |
7 |
125,442,188 (GRCm39) |
missense |
probably benign |
0.17 |
R8154:Katnip
|
UTSW |
7 |
125,412,802 (GRCm39) |
missense |
probably damaging |
0.98 |
R8204:Katnip
|
UTSW |
7 |
125,449,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R8359:Katnip
|
UTSW |
7 |
125,468,023 (GRCm39) |
critical splice donor site |
probably null |
|
R8700:Katnip
|
UTSW |
7 |
125,429,042 (GRCm39) |
splice site |
probably benign |
|
R8812:Katnip
|
UTSW |
7 |
125,396,867 (GRCm39) |
missense |
probably benign |
0.26 |
R8942:Katnip
|
UTSW |
7 |
125,449,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R9216:Katnip
|
UTSW |
7 |
125,471,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R9254:Katnip
|
UTSW |
7 |
125,469,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9263:Katnip
|
UTSW |
7 |
125,469,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9379:Katnip
|
UTSW |
7 |
125,469,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Katnip
|
UTSW |
7 |
125,442,092 (GRCm39) |
missense |
probably benign |
0.04 |
R9657:Katnip
|
UTSW |
7 |
125,441,956 (GRCm39) |
missense |
probably benign |
|
U24488:Katnip
|
UTSW |
7 |
125,369,853 (GRCm39) |
missense |
probably damaging |
0.96 |
|