Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
G |
11: 84,185,813 (GRCm39) |
D116G |
possibly damaging |
Het |
Adam6a |
G |
A |
12: 113,508,196 (GRCm39) |
G190S |
probably benign |
Het |
Adnp |
G |
A |
2: 168,025,367 (GRCm39) |
R643* |
probably null |
Het |
Akap6 |
A |
G |
12: 52,933,633 (GRCm39) |
D375G |
possibly damaging |
Het |
Aldh1l2 |
G |
T |
10: 83,343,975 (GRCm39) |
A480E |
probably benign |
Het |
Ccdc175 |
T |
A |
12: 72,148,821 (GRCm39) |
Q779L |
possibly damaging |
Het |
Dnah7b |
T |
G |
1: 46,273,324 (GRCm39) |
L2484* |
probably null |
Het |
Dnajc21 |
T |
C |
15: 10,462,430 (GRCm39) |
Y65C |
possibly damaging |
Het |
Dnhd1 |
C |
A |
7: 105,333,294 (GRCm39) |
N255K |
probably benign |
Het |
Efhc1 |
G |
T |
1: 21,037,593 (GRCm39) |
G257W |
probably damaging |
Het |
Fars2 |
C |
A |
13: 36,389,026 (GRCm39) |
L172I |
probably benign |
Het |
Fat4 |
T |
C |
3: 38,945,846 (GRCm39) |
Y1580H |
probably damaging |
Het |
Fli1 |
T |
A |
9: 32,339,326 (GRCm39) |
N253Y |
probably benign |
Het |
Foxd3 |
G |
T |
4: 99,545,151 (GRCm39) |
C97F |
probably damaging |
Het |
Gem |
C |
A |
4: 11,711,170 (GRCm39) |
D120E |
possibly damaging |
Het |
Ighv10-3 |
A |
G |
12: 114,487,299 (GRCm39) |
C41R |
probably damaging |
Het |
Kcnab3 |
A |
G |
11: 69,217,553 (GRCm39) |
S16G |
probably benign |
Het |
Keg1 |
T |
G |
19: 12,693,409 (GRCm39) |
V154G |
probably benign |
Het |
Lrrc45 |
G |
A |
11: 120,611,148 (GRCm39) |
R602H |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,598,292 (GRCm39) |
D591G |
possibly damaging |
Het |
Mmp10 |
T |
A |
9: 7,503,550 (GRCm39) |
V140D |
probably damaging |
Het |
Nat8f2 |
A |
T |
6: 85,845,194 (GRCm39) |
M56K |
probably benign |
Het |
Nckipsd |
T |
C |
9: 108,692,153 (GRCm39) |
F525L |
probably damaging |
Het |
Or10ak7 |
A |
G |
4: 118,791,347 (GRCm39) |
S233P |
probably damaging |
Het |
Or10j7 |
T |
A |
1: 173,011,120 (GRCm39) |
K294* |
probably null |
Het |
Or6c6c |
G |
T |
10: 129,541,155 (GRCm39) |
S136I |
possibly damaging |
Het |
P2ry12 |
T |
A |
3: 59,125,178 (GRCm39) |
M166L |
possibly damaging |
Het |
Palm3 |
T |
C |
8: 84,756,074 (GRCm39) |
S529P |
possibly damaging |
Het |
Pdilt |
A |
T |
7: 119,094,220 (GRCm39) |
Y344N |
probably damaging |
Het |
Pip4k2b |
A |
T |
11: 97,611,188 (GRCm39) |
N309K |
probably benign |
Het |
Pkd1l1 |
C |
T |
11: 8,912,708 (GRCm39) |
V166I |
|
Het |
Plxdc2 |
C |
T |
2: 16,716,894 (GRCm39) |
S377L |
probably benign |
Het |
Rc3h2 |
A |
T |
2: 37,295,344 (GRCm39) |
V224E |
possibly damaging |
Het |
Stk32c |
T |
A |
7: 138,685,220 (GRCm39) |
D428V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,644,951 (GRCm39) |
D12968G |
probably damaging |
Het |
Tulp2 |
G |
T |
7: 45,170,451 (GRCm39) |
V457F |
possibly damaging |
Het |
Vcan |
A |
T |
13: 89,839,908 (GRCm39) |
S1879T |
probably damaging |
Het |
Vmn1r51 |
T |
C |
6: 90,106,437 (GRCm39) |
Y118H |
probably benign |
Het |
Zfat |
A |
C |
15: 68,096,693 (GRCm39) |
V40G |
possibly 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 |
IGL02833:Katnip
|
APN |
7 |
125,449,584 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|