Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700011L22Rik |
C |
T |
8: 79,974,922 (GRCm39) |
E54K |
probably benign |
Het |
Adgra1 |
A |
G |
7: 139,425,510 (GRCm39) |
T8A |
probably benign |
Het |
Alms1 |
A |
G |
6: 85,596,629 (GRCm39) |
Y954C |
probably damaging |
Het |
AU021092 |
A |
C |
16: 5,034,626 (GRCm39) |
F199V |
possibly damaging |
Het |
Bahcc1 |
C |
T |
11: 120,174,184 (GRCm39) |
P1648L |
probably benign |
Het |
Cacna1s |
T |
A |
1: 136,034,756 (GRCm39) |
C1319S |
possibly damaging |
Het |
Capn13 |
G |
A |
17: 73,646,396 (GRCm39) |
P339L |
probably benign |
Het |
Ccdc39 |
A |
T |
3: 33,874,044 (GRCm39) |
M596K |
probably damaging |
Het |
Cfap418 |
A |
G |
4: 10,898,014 (GRCm39) |
T199A |
probably benign |
Het |
Cntn5 |
A |
G |
9: 9,781,668 (GRCm39) |
|
probably benign |
Het |
Cyth4 |
A |
G |
15: 78,494,002 (GRCm39) |
K159E |
probably damaging |
Het |
Dgkz |
C |
A |
2: 91,769,975 (GRCm39) |
R563L |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,889,621 (GRCm39) |
E718G |
probably benign |
Het |
Dop1a |
T |
C |
9: 86,403,048 (GRCm39) |
L1416P |
probably damaging |
Het |
Dstyk |
G |
A |
1: 132,377,464 (GRCm39) |
A110T |
probably damaging |
Het |
Eif1 |
A |
G |
11: 100,211,650 (GRCm39) |
K95E |
probably damaging |
Het |
Espnl |
A |
G |
1: 91,249,943 (GRCm39) |
D30G |
probably benign |
Het |
Gast |
T |
C |
11: 100,227,636 (GRCm39) |
S73P |
probably damaging |
Het |
Gmppb |
T |
C |
9: 107,927,773 (GRCm39) |
Y176H |
probably damaging |
Het |
Grap2 |
A |
G |
15: 80,507,947 (GRCm39) |
T4A |
possibly damaging |
Het |
Grm8 |
T |
G |
6: 28,125,635 (GRCm39) |
N164H |
possibly damaging |
Het |
Gstm3 |
G |
A |
3: 107,871,551 (GRCm39) |
T210I |
probably benign |
Het |
Gtf3c3 |
A |
G |
1: 54,463,166 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
A |
G |
2: 31,242,897 (GRCm39) |
|
probably null |
Het |
Icam2 |
A |
G |
11: 106,271,648 (GRCm39) |
L94P |
probably damaging |
Het |
Jarid2 |
T |
A |
13: 45,056,307 (GRCm39) |
N365K |
probably benign |
Het |
Kank4 |
A |
G |
4: 98,668,370 (GRCm39) |
S26P |
probably damaging |
Het |
Lgr4 |
A |
G |
2: 109,838,542 (GRCm39) |
K498E |
probably benign |
Het |
Meltf |
A |
G |
16: 31,703,816 (GRCm39) |
H181R |
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Nf1 |
A |
G |
11: 79,450,347 (GRCm39) |
D511G |
probably null |
Het |
Nhlrc3 |
A |
G |
3: 53,366,052 (GRCm39) |
V147A |
possibly damaging |
Het |
Nrap |
C |
T |
19: 56,310,211 (GRCm39) |
D1595N |
probably damaging |
Het |
Or1e16 |
T |
C |
11: 73,286,776 (GRCm39) |
Q24R |
probably benign |
Het |
Or5p4 |
A |
T |
7: 107,680,378 (GRCm39) |
I126F |
probably damaging |
Het |
Or6c212 |
T |
A |
10: 129,558,918 (GRCm39) |
D165V |
possibly damaging |
Het |
Or6n2 |
T |
A |
1: 173,897,474 (GRCm39) |
N203K |
probably damaging |
Het |
Pak3 |
G |
A |
X: 142,492,727 (GRCm39) |
V87I |
probably damaging |
Het |
Pgm2l1 |
T |
C |
7: 99,901,474 (GRCm39) |
V121A |
probably benign |
Het |
Phf19 |
A |
G |
2: 34,789,670 (GRCm39) |
L350P |
probably damaging |
Het |
Phf8 |
T |
C |
X: 150,355,572 (GRCm39) |
S512P |
possibly damaging |
Het |
Phkb |
G |
T |
8: 86,648,858 (GRCm39) |
E225* |
probably null |
Het |
Pif1 |
T |
A |
9: 65,495,588 (GRCm39) |
V166E |
probably damaging |
Het |
Plaa |
T |
C |
4: 94,458,125 (GRCm39) |
D615G |
probably damaging |
Het |
Prpf4b |
T |
C |
13: 35,067,665 (GRCm39) |
|
probably benign |
Het |
Rxra |
T |
C |
2: 27,646,272 (GRCm39) |
C374R |
probably damaging |
Het |
Septin3 |
T |
C |
15: 82,170,630 (GRCm39) |
|
probably benign |
Het |
Skint4 |
G |
T |
4: 111,975,378 (GRCm39) |
V113L |
probably damaging |
Het |
Slc16a10 |
G |
C |
10: 39,932,620 (GRCm39) |
H314D |
possibly damaging |
Het |
Slc22a15 |
C |
T |
3: 101,804,590 (GRCm39) |
G145D |
probably damaging |
Het |
Slc28a1 |
A |
T |
7: 80,775,969 (GRCm39) |
I222F |
probably damaging |
Het |
Slc43a2 |
T |
C |
11: 75,454,424 (GRCm39) |
L323P |
probably benign |
Het |
Sorbs3 |
A |
G |
14: 70,436,800 (GRCm39) |
|
probably benign |
Het |
Spink10 |
C |
T |
18: 62,786,485 (GRCm39) |
|
probably benign |
Het |
Suclg2 |
A |
T |
6: 95,474,649 (GRCm39) |
I372N |
probably damaging |
Het |
Sun1 |
C |
A |
5: 139,211,117 (GRCm39) |
C164* |
probably null |
Het |
Tax1bp1 |
T |
C |
6: 52,719,770 (GRCm39) |
F453L |
probably benign |
Het |
Tmem54 |
A |
G |
4: 129,002,013 (GRCm39) |
N9S |
probably benign |
Het |
Tmx4 |
A |
G |
2: 134,462,497 (GRCm39) |
W145R |
probably damaging |
Het |
Top1 |
A |
G |
2: 160,544,688 (GRCm39) |
H268R |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,641,075 (GRCm39) |
L13598P |
probably damaging |
Het |
Vmn1r40 |
A |
G |
6: 89,691,991 (GRCm39) |
I269M |
probably benign |
Het |
Wdr7 |
G |
T |
18: 63,853,907 (GRCm39) |
R80L |
probably benign |
Het |
Zap70 |
A |
T |
1: 36,810,223 (GRCm39) |
Q111L |
possibly damaging |
Het |
Zfp808 |
T |
A |
13: 62,319,897 (GRCm39) |
H375Q |
probably damaging |
Het |
Zkscan2 |
A |
T |
7: 123,094,365 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Iqcm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01895:Iqcm
|
APN |
8 |
76,615,188 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Iqcm
|
APN |
8 |
76,281,511 (GRCm39) |
utr 5 prime |
probably benign |
|
R0056:Iqcm
|
UTSW |
8 |
76,480,014 (GRCm39) |
missense |
probably benign |
|
R2146:Iqcm
|
UTSW |
8 |
76,615,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Iqcm
|
UTSW |
8 |
76,441,404 (GRCm39) |
missense |
probably benign |
|
R3801:Iqcm
|
UTSW |
8 |
76,396,021 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3834:Iqcm
|
UTSW |
8 |
76,304,380 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3897:Iqcm
|
UTSW |
8 |
76,480,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Iqcm
|
UTSW |
8 |
76,356,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4448:Iqcm
|
UTSW |
8 |
76,356,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4450:Iqcm
|
UTSW |
8 |
76,356,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4687:Iqcm
|
UTSW |
8 |
76,489,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Iqcm
|
UTSW |
8 |
76,615,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Iqcm
|
UTSW |
8 |
76,472,980 (GRCm39) |
missense |
probably damaging |
0.99 |
R4856:Iqcm
|
UTSW |
8 |
76,615,228 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4886:Iqcm
|
UTSW |
8 |
76,615,228 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5063:Iqcm
|
UTSW |
8 |
76,472,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Iqcm
|
UTSW |
8 |
76,441,417 (GRCm39) |
missense |
probably benign |
|
R6403:Iqcm
|
UTSW |
8 |
76,304,624 (GRCm39) |
critical splice donor site |
probably null |
|
R6667:Iqcm
|
UTSW |
8 |
76,479,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R7187:Iqcm
|
UTSW |
8 |
76,480,044 (GRCm39) |
missense |
probably benign |
0.22 |
R7263:Iqcm
|
UTSW |
8 |
76,489,701 (GRCm39) |
missense |
probably benign |
|
R7701:Iqcm
|
UTSW |
8 |
76,281,539 (GRCm39) |
missense |
probably benign |
0.02 |
R7916:Iqcm
|
UTSW |
8 |
76,304,578 (GRCm39) |
missense |
probably benign |
|
R7938:Iqcm
|
UTSW |
8 |
76,304,596 (GRCm39) |
missense |
probably benign |
|
R7974:Iqcm
|
UTSW |
8 |
76,281,520 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R8039:Iqcm
|
UTSW |
8 |
76,489,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R8311:Iqcm
|
UTSW |
8 |
76,480,118 (GRCm39) |
splice site |
probably benign |
|
R8703:Iqcm
|
UTSW |
8 |
76,615,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9175:Iqcm
|
UTSW |
8 |
76,710,867 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9475:Iqcm
|
UTSW |
8 |
76,480,083 (GRCm39) |
missense |
probably damaging |
1.00 |
RF002:Iqcm
|
UTSW |
8 |
76,304,527 (GRCm39) |
missense |
probably benign |
0.01 |
X0018:Iqcm
|
UTSW |
8 |
76,710,840 (GRCm39) |
nonsense |
probably null |
|
|