Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
G |
T |
11: 9,247,629 (GRCm39) |
V2459F |
probably benign |
Het |
Acot1 |
T |
C |
12: 84,061,314 (GRCm39) |
Y207H |
probably damaging |
Het |
Anapc1 |
A |
G |
2: 128,465,476 (GRCm39) |
V1668A |
possibly damaging |
Het |
Atr |
T |
A |
9: 95,833,589 (GRCm39) |
I2613N |
probably damaging |
Het |
Baz2b |
A |
G |
2: 59,731,957 (GRCm39) |
I2027T |
possibly damaging |
Het |
C2cd3 |
T |
G |
7: 100,090,296 (GRCm39) |
H466Q |
probably damaging |
Het |
Cdc14b |
T |
A |
13: 64,396,225 (GRCm39) |
I15F |
probably benign |
Het |
Cep135 |
G |
T |
5: 76,759,561 (GRCm39) |
K438N |
possibly damaging |
Het |
Cnot1 |
T |
C |
8: 96,466,476 (GRCm39) |
D1587G |
probably damaging |
Het |
Cxcl16 |
C |
A |
11: 70,349,631 (GRCm39) |
V65L |
possibly damaging |
Het |
Dhx36 |
T |
A |
3: 62,382,699 (GRCm39) |
T783S |
probably benign |
Het |
Disp3 |
T |
C |
4: 148,356,389 (GRCm39) |
N157S |
probably benign |
Het |
Efcab3 |
G |
T |
11: 104,624,547 (GRCm39) |
|
probably null |
Het |
Fem1al |
A |
T |
11: 29,774,669 (GRCm39) |
S263T |
probably benign |
Het |
Gfod2 |
T |
C |
8: 106,444,177 (GRCm39) |
N122S |
possibly damaging |
Het |
Grin3b |
T |
A |
10: 79,808,731 (GRCm39) |
D160E |
probably benign |
Het |
Grm7 |
G |
T |
6: 110,623,309 (GRCm39) |
V161F |
probably damaging |
Het |
Htr1b |
C |
A |
9: 81,514,404 (GRCm39) |
A68S |
probably benign |
Het |
Ifit2 |
A |
T |
19: 34,550,544 (GRCm39) |
D28V |
possibly damaging |
Het |
Igsf9b |
G |
A |
9: 27,220,774 (GRCm39) |
V47I |
possibly damaging |
Het |
Kif24 |
A |
G |
4: 41,413,827 (GRCm39) |
|
probably null |
Het |
Klhl25 |
T |
C |
7: 75,516,480 (GRCm39) |
V462A |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
L3mbtl3 |
A |
G |
10: 26,203,639 (GRCm39) |
V397A |
unknown |
Het |
Lpcat2 |
C |
A |
8: 93,599,734 (GRCm39) |
P234Q |
probably benign |
Het |
Lrp1b |
A |
C |
2: 40,793,077 (GRCm39) |
C2532W |
probably damaging |
Het |
Malt1 |
T |
C |
18: 65,609,300 (GRCm39) |
V768A |
probably benign |
Het |
Mindy3 |
A |
T |
2: 12,401,020 (GRCm39) |
W233R |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,249,736 (GRCm39) |
K1054R |
probably damaging |
Het |
Nin |
T |
A |
12: 70,061,712 (GRCm39) |
T2051S |
probably benign |
Het |
Or10j5 |
C |
A |
1: 172,784,647 (GRCm39) |
A95E |
probably benign |
Het |
Or51ac3 |
A |
G |
7: 103,213,742 (GRCm39) |
F248S |
probably benign |
Het |
Pcsk1 |
T |
C |
13: 75,260,838 (GRCm39) |
S354P |
possibly damaging |
Het |
Pilra |
T |
C |
5: 137,829,576 (GRCm39) |
T160A |
probably benign |
Het |
Plekha5 |
G |
C |
6: 140,537,414 (GRCm39) |
E540D |
probably benign |
Het |
Prps2 |
T |
A |
X: 166,146,545 (GRCm39) |
K176* |
probably null |
Het |
Rasgrf2 |
C |
A |
13: 92,038,796 (GRCm39) |
D1017Y |
probably damaging |
Het |
Slc15a4 |
A |
G |
5: 127,681,600 (GRCm39) |
|
probably null |
Het |
Spsb1 |
T |
C |
4: 149,991,232 (GRCm39) |
H112R |
probably damaging |
Het |
Srd5a3 |
T |
A |
5: 76,295,547 (GRCm39) |
F79Y |
probably damaging |
Het |
Stxbp4 |
C |
T |
11: 90,385,470 (GRCm39) |
W506* |
probably null |
Het |
Timeless |
C |
A |
10: 128,083,211 (GRCm39) |
Q653K |
probably benign |
Het |
Trio |
G |
A |
15: 27,749,883 (GRCm39) |
Q1129* |
probably null |
Het |
Vrk3 |
C |
T |
7: 44,424,866 (GRCm39) |
T427M |
probably benign |
Het |
Zzef1 |
T |
A |
11: 72,714,334 (GRCm39) |
S275T |
probably damaging |
Het |
|
Other mutations in Ifna15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01575:Ifna15
|
APN |
4 |
88,476,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01757:Ifna15
|
APN |
4 |
88,476,322 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01824:Ifna15
|
APN |
4 |
88,476,020 (GRCm39) |
missense |
probably benign |
0.00 |
R3853:Ifna15
|
UTSW |
4 |
88,476,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R4357:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R4358:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R5038:Ifna15
|
UTSW |
4 |
88,476,266 (GRCm39) |
missense |
probably benign |
0.03 |
R5372:Ifna15
|
UTSW |
4 |
88,476,338 (GRCm39) |
missense |
probably damaging |
0.97 |
R6036:Ifna15
|
UTSW |
4 |
88,476,310 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6036:Ifna15
|
UTSW |
4 |
88,476,310 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7347:Ifna15
|
UTSW |
4 |
88,476,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R8097:Ifna15
|
UTSW |
4 |
88,475,938 (GRCm39) |
missense |
probably benign |
0.01 |
R8132:Ifna15
|
UTSW |
4 |
88,475,920 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8824:Ifna15
|
UTSW |
4 |
88,475,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R9349:Ifna15
|
UTSW |
4 |
88,476,283 (GRCm39) |
missense |
probably benign |
0.10 |
|