Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef12 |
T |
C |
9: 42,916,919 (GRCm39) |
D409G |
probably damaging |
Het |
AW551984 |
A |
C |
9: 39,500,382 (GRCm39) |
L792R |
possibly damaging |
Het |
Cep192 |
A |
G |
18: 67,974,350 (GRCm39) |
E1151G |
probably damaging |
Het |
Cfap44 |
C |
A |
16: 44,301,746 (GRCm39) |
P1828Q |
probably damaging |
Het |
Chid1 |
A |
T |
7: 141,076,603 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
C |
A |
9: 105,659,390 (GRCm39) |
L518F |
probably damaging |
Het |
Ctsz |
C |
T |
2: 174,270,891 (GRCm39) |
R201K |
probably benign |
Het |
Diras1 |
T |
C |
10: 80,858,119 (GRCm39) |
Y44C |
probably damaging |
Het |
Grip1 |
T |
C |
10: 119,778,818 (GRCm39) |
V159A |
probably damaging |
Het |
Hpd |
T |
C |
5: 123,317,420 (GRCm39) |
|
probably benign |
Het |
Jag2 |
T |
C |
12: 112,879,131 (GRCm39) |
N463S |
probably benign |
Het |
Kmt2a |
C |
A |
9: 44,741,810 (GRCm39) |
|
probably benign |
Het |
Myo5a |
A |
G |
9: 75,118,429 (GRCm39) |
N1619D |
probably benign |
Het |
Ncbp1 |
A |
G |
4: 46,168,449 (GRCm39) |
|
probably null |
Het |
Or12d13 |
G |
T |
17: 37,647,415 (GRCm39) |
A236E |
probably damaging |
Het |
Or2n1b |
C |
T |
17: 38,460,280 (GRCm39) |
T267I |
possibly damaging |
Het |
Pacsin2 |
G |
T |
15: 83,272,864 (GRCm39) |
A154E |
possibly damaging |
Het |
Plcd4 |
A |
T |
1: 74,603,539 (GRCm39) |
I647F |
probably damaging |
Het |
Prdm10 |
C |
T |
9: 31,268,589 (GRCm39) |
A846V |
probably damaging |
Het |
Ptgs2 |
G |
T |
1: 149,978,526 (GRCm39) |
G213* |
probably null |
Het |
Rcan3 |
C |
T |
4: 135,152,706 (GRCm39) |
S5N |
probably benign |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Serpinc1 |
A |
G |
1: 160,830,029 (GRCm39) |
N465S |
probably benign |
Het |
Slc40a1 |
T |
C |
1: 45,951,534 (GRCm39) |
I208V |
possibly damaging |
Het |
Vcl |
C |
T |
14: 20,979,643 (GRCm39) |
Q19* |
probably null |
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 |
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 |
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 |
|