Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad10 |
A |
G |
5: 121,767,993 (GRCm39) |
V819A |
possibly damaging |
Het |
Adgrd1 |
A |
T |
5: 129,209,809 (GRCm39) |
N279Y |
probably damaging |
Het |
Aplp2 |
C |
A |
9: 31,089,379 (GRCm39) |
|
probably benign |
Het |
Armc8 |
T |
C |
9: 99,409,122 (GRCm39) |
|
probably benign |
Het |
B3gnt5 |
A |
G |
16: 19,588,360 (GRCm39) |
D193G |
probably damaging |
Het |
Cacng1 |
A |
G |
11: 107,595,145 (GRCm39) |
F144S |
probably damaging |
Het |
Cfap91 |
T |
A |
16: 38,154,140 (GRCm39) |
D135V |
possibly damaging |
Het |
Dnm3 |
T |
A |
1: 162,183,001 (GRCm39) |
T105S |
probably damaging |
Het |
Efcab6 |
T |
A |
15: 83,763,649 (GRCm39) |
I1228F |
probably damaging |
Het |
Erc2 |
A |
G |
14: 27,498,937 (GRCm39) |
D271G |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,908,433 (GRCm39) |
Y2523C |
probably damaging |
Het |
Fhl4 |
A |
G |
10: 84,934,035 (GRCm39) |
F249L |
probably damaging |
Het |
Gm17782 |
T |
C |
17: 36,472,958 (GRCm39) |
|
probably benign |
Het |
Gm4787 |
A |
G |
12: 81,425,502 (GRCm39) |
Y219H |
probably damaging |
Het |
Hk1 |
A |
G |
10: 62,128,138 (GRCm39) |
L328P |
probably benign |
Het |
Hspa12a |
T |
A |
19: 58,797,983 (GRCm39) |
Y245F |
probably benign |
Het |
Kbtbd12 |
T |
C |
6: 88,595,371 (GRCm39) |
Y153C |
probably damaging |
Het |
Kcnd2 |
A |
T |
6: 21,726,194 (GRCm39) |
R562S |
probably benign |
Het |
Lct |
T |
C |
1: 128,235,988 (GRCm39) |
S340G |
probably benign |
Het |
Mettl25 |
C |
A |
10: 105,662,185 (GRCm39) |
G262W |
probably damaging |
Het |
Mindy3 |
G |
A |
2: 12,369,294 (GRCm39) |
Q142* |
probably null |
Het |
Optn |
T |
C |
2: 5,039,833 (GRCm39) |
E318G |
probably damaging |
Het |
Or8j3 |
A |
T |
2: 86,028,363 (GRCm39) |
H244Q |
probably damaging |
Het |
Pan2 |
T |
C |
10: 128,148,768 (GRCm39) |
S443P |
probably benign |
Het |
Parva |
A |
G |
7: 112,175,646 (GRCm39) |
D259G |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,448,269 (GRCm39) |
L3816Q |
probably damaging |
Het |
Polq |
T |
C |
16: 36,880,737 (GRCm39) |
F967S |
probably benign |
Het |
Prdm16 |
T |
C |
4: 154,425,334 (GRCm39) |
N817S |
probably damaging |
Het |
Ptprt |
C |
A |
2: 161,449,372 (GRCm39) |
|
probably benign |
Het |
Rbbp8nl |
T |
A |
2: 179,923,236 (GRCm39) |
S154C |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
Slit1 |
T |
C |
19: 41,640,122 (GRCm39) |
I169V |
probably damaging |
Het |
Smyd4 |
G |
T |
11: 75,280,890 (GRCm39) |
|
probably benign |
Het |
Tial1 |
A |
G |
7: 128,045,607 (GRCm39) |
Y326H |
probably benign |
Het |
Tmem198b |
A |
G |
10: 128,638,320 (GRCm39) |
L81P |
probably damaging |
Het |
Tmem94 |
T |
A |
11: 115,687,227 (GRCm39) |
C1115* |
probably null |
Het |
Tns3 |
A |
G |
11: 8,387,141 (GRCm39) |
S1349P |
probably damaging |
Het |
Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
Zfp106 |
A |
T |
2: 120,376,395 (GRCm39) |
|
probably null |
Het |
Zfp119b |
T |
C |
17: 56,246,793 (GRCm39) |
E99G |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,012,986 (GRCm39) |
C503S |
probably damaging |
Het |
Zfyve19 |
G |
A |
2: 119,042,496 (GRCm39) |
|
probably null |
Het |
Zxdc |
G |
T |
6: 90,359,352 (GRCm39) |
K661N |
probably damaging |
Het |
|
Other mutations in 4932438H23Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00686:4932438H23Rik
|
APN |
16 |
90,852,489 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01934:4932438H23Rik
|
APN |
16 |
90,852,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02060:4932438H23Rik
|
APN |
16 |
90,852,603 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:4932438H23Rik
|
APN |
16 |
90,853,085 (GRCm39) |
missense |
probably benign |
0.23 |
PIT4810001:4932438H23Rik
|
UTSW |
16 |
90,852,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:4932438H23Rik
|
UTSW |
16 |
90,852,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R0932:4932438H23Rik
|
UTSW |
16 |
90,852,995 (GRCm39) |
missense |
probably benign |
0.00 |
R4591:4932438H23Rik
|
UTSW |
16 |
90,852,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R6472:4932438H23Rik
|
UTSW |
16 |
90,852,891 (GRCm39) |
missense |
probably benign |
0.00 |
R6513:4932438H23Rik
|
UTSW |
16 |
90,852,654 (GRCm39) |
missense |
probably benign |
0.00 |
R7067:4932438H23Rik
|
UTSW |
16 |
90,852,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:4932438H23Rik
|
UTSW |
16 |
90,852,744 (GRCm39) |
missense |
probably benign |
0.06 |
R8369:4932438H23Rik
|
UTSW |
16 |
90,852,657 (GRCm39) |
missense |
probably benign |
0.07 |
R8469:4932438H23Rik
|
UTSW |
16 |
90,852,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R8508:4932438H23Rik
|
UTSW |
16 |
90,852,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:4932438H23Rik
|
UTSW |
16 |
90,852,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:4932438H23Rik
|
UTSW |
16 |
90,852,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:4932438H23Rik
|
UTSW |
16 |
90,853,046 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9335:4932438H23Rik
|
UTSW |
16 |
90,852,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:4932438H23Rik
|
UTSW |
16 |
90,853,096 (GRCm39) |
missense |
probably benign |
0.23 |
Z1088:4932438H23Rik
|
UTSW |
16 |
90,852,701 (GRCm39) |
missense |
probably benign |
0.01 |
|