Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,285,232 (GRCm39) |
T3289S |
probably damaging |
Het |
Actr1b |
G |
T |
1: 36,740,534 (GRCm39) |
Q240K |
probably benign |
Het |
Adamts19 |
T |
C |
18: 59,034,048 (GRCm39) |
V341A |
probably damaging |
Het |
Akirin2 |
C |
A |
4: 34,551,148 (GRCm39) |
S35* |
probably null |
Het |
Alg3 |
G |
T |
16: 20,427,765 (GRCm39) |
Q90K |
probably benign |
Het |
Alox12 |
C |
T |
11: 70,138,153 (GRCm39) |
R394H |
possibly damaging |
Het |
Ankrd17 |
A |
C |
5: 90,411,134 (GRCm39) |
M1387R |
probably damaging |
Het |
Anp32b |
T |
G |
4: 46,468,592 (GRCm39) |
F121V |
possibly damaging |
Het |
Atp2b2 |
A |
G |
6: 113,740,566 (GRCm39) |
V815A |
probably damaging |
Het |
Atxn7l1 |
T |
C |
12: 33,417,420 (GRCm39) |
L527S |
probably benign |
Het |
B9d2 |
C |
T |
7: 25,385,462 (GRCm39) |
L91F |
possibly damaging |
Het |
Bcl2l11 |
T |
A |
2: 128,000,221 (GRCm39) |
I188N |
probably damaging |
Het |
Bnc2 |
A |
C |
4: 84,210,138 (GRCm39) |
S744A |
probably benign |
Het |
Casr |
T |
G |
16: 36,330,414 (GRCm39) |
M307L |
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cd109 |
TTATA |
TTATATATA |
9: 78,619,813 (GRCm39) |
|
probably benign |
Het |
Cd22 |
A |
G |
7: 30,575,449 (GRCm39) |
S198P |
probably benign |
Het |
Cd37 |
C |
A |
7: 44,886,622 (GRCm39) |
V99L |
probably benign |
Het |
Cdkn1c |
A |
G |
7: 143,013,964 (GRCm39) |
S161P |
possibly damaging |
Het |
Chi3l1 |
G |
T |
1: 134,111,919 (GRCm39) |
|
probably null |
Het |
Col4a2 |
T |
C |
8: 11,498,198 (GRCm39) |
F1669S |
probably damaging |
Het |
Dchs2 |
A |
T |
3: 83,261,493 (GRCm39) |
H2587L |
probably benign |
Het |
Ddx19a |
A |
T |
8: 111,710,228 (GRCm39) |
M124K |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,341,933 (GRCm39) |
H1244L |
possibly damaging |
Het |
Dnpep |
G |
A |
1: 75,292,329 (GRCm39) |
P165L |
probably damaging |
Het |
Dpp3 |
T |
C |
19: 4,973,172 (GRCm39) |
R141G |
probably benign |
Het |
Dpysl3 |
T |
C |
18: 43,462,814 (GRCm39) |
D521G |
probably damaging |
Het |
Dusp4 |
T |
A |
8: 35,284,345 (GRCm39) |
M220K |
probably damaging |
Het |
Duxf4 |
G |
A |
10: 58,071,711 (GRCm39) |
P168S |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,613,833 (GRCm39) |
L391Q |
probably damaging |
Het |
Edrf1 |
A |
C |
7: 133,273,207 (GRCm39) |
I1221L |
probably benign |
Het |
Elavl2 |
A |
G |
4: 91,199,847 (GRCm39) |
L12P |
probably benign |
Het |
Fastkd3 |
T |
A |
13: 68,733,071 (GRCm39) |
V464D |
probably damaging |
Het |
Flt4 |
C |
A |
11: 49,527,598 (GRCm39) |
N920K |
probably benign |
Het |
Gimap3 |
T |
C |
6: 48,742,259 (GRCm39) |
T224A |
probably benign |
Het |
Gm9772 |
T |
A |
17: 22,225,565 (GRCm39) |
K112* |
probably null |
Het |
Gp5 |
C |
A |
16: 30,127,976 (GRCm39) |
V233L |
|
Het |
Gpr25 |
A |
T |
1: 136,188,026 (GRCm39) |
W196R |
probably benign |
Het |
Hs3st4 |
G |
A |
7: 123,582,680 (GRCm39) |
G93S |
probably damaging |
Het |
Igsf10 |
A |
G |
3: 59,236,668 (GRCm39) |
L1171S |
probably benign |
Het |
Itgb7 |
C |
T |
15: 102,126,359 (GRCm39) |
G526S |
possibly damaging |
Het |
Kcnh8 |
G |
A |
17: 53,141,642 (GRCm39) |
C295Y |
probably damaging |
Het |
Klhl8 |
A |
G |
5: 104,015,709 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
A |
15: 101,726,317 (GRCm39) |
I74F |
unknown |
Het |
Lamp5 |
G |
T |
2: 135,911,054 (GRCm39) |
M262I |
probably benign |
Het |
Lrp5 |
G |
T |
19: 3,680,156 (GRCm39) |
R443S |
possibly damaging |
Het |
Lrrc66 |
G |
T |
5: 73,765,267 (GRCm39) |
A592E |
probably benign |
Het |
Lrrc66 |
C |
T |
5: 73,765,268 (GRCm39) |
A592T |
probably benign |
Het |
Mettl23 |
T |
A |
11: 116,744,865 (GRCm39) |
V93D |
unknown |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Mkrn2os |
G |
A |
6: 115,562,325 (GRCm39) |
R213W |
probably benign |
Het |
Mrps36 |
T |
A |
13: 100,877,715 (GRCm39) |
I22L |
probably damaging |
Het |
Msantd5f4 |
A |
G |
4: 73,557,185 (GRCm39) |
N6S |
possibly damaging |
Het |
Myocd |
T |
C |
11: 65,077,795 (GRCm39) |
R667G |
probably benign |
Het |
Ndst3 |
T |
C |
3: 123,465,549 (GRCm39) |
N141S |
probably benign |
Het |
Neu2 |
A |
T |
1: 87,524,965 (GRCm39) |
R317* |
probably null |
Het |
Nf1 |
G |
T |
11: 79,364,168 (GRCm39) |
V1533F |
probably damaging |
Het |
Npy4r |
T |
A |
14: 33,869,083 (GRCm39) |
R68S |
possibly damaging |
Het |
Nr1h5 |
T |
C |
3: 102,853,427 (GRCm39) |
H360R |
probably null |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or4f14c |
T |
C |
2: 111,941,441 (GRCm39) |
D52G |
probably damaging |
Het |
Or9s15 |
T |
C |
1: 92,524,978 (GRCm39) |
S246P |
probably damaging |
Het |
Osmr |
A |
C |
15: 6,882,027 (GRCm39) |
V39G |
probably damaging |
Het |
Plekhm2 |
T |
C |
4: 141,359,732 (GRCm39) |
D345G |
possibly damaging |
Het |
Prkaa2 |
G |
T |
4: 104,906,600 (GRCm39) |
S165* |
probably null |
Het |
Qser1 |
A |
T |
2: 104,593,292 (GRCm39) |
F1575Y |
possibly damaging |
Het |
Rasl11a |
C |
A |
5: 146,782,107 (GRCm39) |
D27E |
probably benign |
Het |
Ret |
A |
T |
6: 118,142,888 (GRCm39) |
Y929* |
probably null |
Het |
Samd9l |
T |
A |
6: 3,373,493 (GRCm39) |
E1256V |
probably benign |
Het |
Scnn1g |
A |
G |
7: 121,341,566 (GRCm39) |
I243V |
possibly damaging |
Het |
Slc6a3 |
C |
T |
13: 73,718,031 (GRCm39) |
R514* |
probably null |
Het |
Sorcs3 |
C |
T |
19: 48,194,809 (GRCm39) |
A64V |
probably benign |
Het |
Sos1 |
G |
T |
17: 80,715,723 (GRCm39) |
N1011K |
probably benign |
Het |
Srbd1 |
C |
A |
17: 86,428,115 (GRCm39) |
A373S |
possibly damaging |
Het |
Tas1r1 |
C |
T |
4: 152,122,833 (GRCm39) |
W4* |
probably null |
Het |
Tcf15 |
C |
T |
2: 151,985,690 (GRCm39) |
R49C |
probably damaging |
Het |
Tex30 |
A |
G |
1: 44,127,136 (GRCm39) |
V124A |
possibly damaging |
Het |
Tgif1 |
T |
C |
17: 71,151,882 (GRCm39) |
D243G |
|
Het |
Tgtp1 |
T |
G |
11: 48,877,916 (GRCm39) |
D263A |
probably damaging |
Het |
Themis3 |
T |
A |
17: 66,862,864 (GRCm39) |
T365S |
probably benign |
Het |
Thoc2l |
C |
A |
5: 104,666,818 (GRCm39) |
P447T |
probably benign |
Het |
Tprg1 |
A |
T |
16: 25,231,662 (GRCm39) |
I213F |
probably damaging |
Het |
Traf4 |
A |
T |
11: 78,052,005 (GRCm39) |
C160S |
probably damaging |
Het |
Trio |
T |
C |
15: 27,732,770 (GRCm39) |
E3037G |
possibly damaging |
Het |
Ttbk2 |
G |
T |
2: 120,575,911 (GRCm39) |
S1022* |
probably null |
Het |
Ttc6 |
T |
C |
12: 57,783,949 (GRCm39) |
Y1803H |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,549,452 (GRCm39) |
Y31742D |
probably benign |
Het |
Ttn |
G |
T |
2: 76,617,595 (GRCm39) |
P16292Q |
probably damaging |
Het |
Ubr5 |
A |
G |
15: 38,002,503 (GRCm39) |
V1510A |
|
Het |
Vac14 |
A |
G |
8: 111,379,869 (GRCm39) |
D389G |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,324,150 (GRCm39) |
D1151G |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,032,266 (GRCm39) |
N558S |
probably damaging |
Het |
|
Other mutations in Ncapg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Ncapg
|
APN |
5 |
45,850,502 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL00777:Ncapg
|
APN |
5 |
45,853,107 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00857:Ncapg
|
APN |
5 |
45,833,927 (GRCm39) |
splice site |
probably null |
|
IGL00916:Ncapg
|
APN |
5 |
45,828,534 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01293:Ncapg
|
APN |
5 |
45,839,196 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01360:Ncapg
|
APN |
5 |
45,831,727 (GRCm39) |
nonsense |
probably null |
|
IGL01462:Ncapg
|
APN |
5 |
45,828,477 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01527:Ncapg
|
APN |
5 |
45,829,726 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01732:Ncapg
|
APN |
5 |
45,851,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01788:Ncapg
|
APN |
5 |
45,828,423 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01871:Ncapg
|
APN |
5 |
45,845,923 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03106:Ncapg
|
APN |
5 |
45,853,010 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03124:Ncapg
|
APN |
5 |
45,828,551 (GRCm39) |
missense |
probably benign |
|
R0086:Ncapg
|
UTSW |
5 |
45,834,086 (GRCm39) |
splice site |
probably null |
|
R0109:Ncapg
|
UTSW |
5 |
45,851,090 (GRCm39) |
splice site |
probably null |
|
R0110:Ncapg
|
UTSW |
5 |
45,850,489 (GRCm39) |
unclassified |
probably benign |
|
R0377:Ncapg
|
UTSW |
5 |
45,851,159 (GRCm39) |
missense |
probably benign |
|
R0432:Ncapg
|
UTSW |
5 |
45,829,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R0637:Ncapg
|
UTSW |
5 |
45,844,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Ncapg
|
UTSW |
5 |
45,838,790 (GRCm39) |
missense |
probably damaging |
0.96 |
R0894:Ncapg
|
UTSW |
5 |
45,837,236 (GRCm39) |
missense |
probably null |
0.24 |
R1069:Ncapg
|
UTSW |
5 |
45,833,272 (GRCm39) |
intron |
probably benign |
|
R1216:Ncapg
|
UTSW |
5 |
45,857,261 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1967:Ncapg
|
UTSW |
5 |
45,857,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R2396:Ncapg
|
UTSW |
5 |
45,835,715 (GRCm39) |
missense |
probably benign |
0.00 |
R3157:Ncapg
|
UTSW |
5 |
45,833,400 (GRCm39) |
missense |
probably benign |
|
R3735:Ncapg
|
UTSW |
5 |
45,853,469 (GRCm39) |
missense |
probably benign |
0.00 |
R3736:Ncapg
|
UTSW |
5 |
45,853,469 (GRCm39) |
missense |
probably benign |
0.00 |
R3887:Ncapg
|
UTSW |
5 |
45,831,705 (GRCm39) |
missense |
probably benign |
|
R4371:Ncapg
|
UTSW |
5 |
45,835,797 (GRCm39) |
missense |
probably benign |
|
R4545:Ncapg
|
UTSW |
5 |
45,828,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Ncapg
|
UTSW |
5 |
45,828,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4558:Ncapg
|
UTSW |
5 |
45,833,986 (GRCm39) |
missense |
probably benign |
0.00 |
R4615:Ncapg
|
UTSW |
5 |
45,844,741 (GRCm39) |
missense |
probably benign |
0.00 |
R4938:Ncapg
|
UTSW |
5 |
45,828,551 (GRCm39) |
missense |
probably benign |
|
R5839:Ncapg
|
UTSW |
5 |
45,829,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R5871:Ncapg
|
UTSW |
5 |
45,853,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R6086:Ncapg
|
UTSW |
5 |
45,850,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6418:Ncapg
|
UTSW |
5 |
45,839,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6617:Ncapg
|
UTSW |
5 |
45,827,474 (GRCm39) |
missense |
probably benign |
0.03 |
R7145:Ncapg
|
UTSW |
5 |
45,827,372 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7408:Ncapg
|
UTSW |
5 |
45,853,135 (GRCm39) |
missense |
probably benign |
0.00 |
R7443:Ncapg
|
UTSW |
5 |
45,829,652 (GRCm39) |
missense |
probably benign |
0.31 |
R7463:Ncapg
|
UTSW |
5 |
45,851,434 (GRCm39) |
splice site |
probably null |
|
R7509:Ncapg
|
UTSW |
5 |
45,853,450 (GRCm39) |
missense |
probably benign |
0.01 |
R7687:Ncapg
|
UTSW |
5 |
45,857,227 (GRCm39) |
missense |
probably benign |
0.03 |
R7919:Ncapg
|
UTSW |
5 |
45,853,390 (GRCm39) |
missense |
probably benign |
0.00 |
R8022:Ncapg
|
UTSW |
5 |
45,839,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Ncapg
|
UTSW |
5 |
45,851,095 (GRCm39) |
missense |
probably benign |
0.00 |
R8261:Ncapg
|
UTSW |
5 |
45,844,730 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8263:Ncapg
|
UTSW |
5 |
45,849,134 (GRCm39) |
missense |
probably benign |
0.44 |
R8324:Ncapg
|
UTSW |
5 |
45,853,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R8333:Ncapg
|
UTSW |
5 |
45,831,805 (GRCm39) |
missense |
probably damaging |
0.96 |
R8742:Ncapg
|
UTSW |
5 |
45,851,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R9026:Ncapg
|
UTSW |
5 |
45,853,115 (GRCm39) |
missense |
probably benign |
0.00 |
R9076:Ncapg
|
UTSW |
5 |
45,833,983 (GRCm39) |
missense |
probably benign |
|
R9122:Ncapg
|
UTSW |
5 |
45,846,015 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9751:Ncapg
|
UTSW |
5 |
45,851,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R9776:Ncapg
|
UTSW |
5 |
45,829,834 (GRCm39) |
missense |
probably damaging |
0.96 |
RF019:Ncapg
|
UTSW |
5 |
45,856,198 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Ncapg
|
UTSW |
5 |
45,837,222 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ncapg
|
UTSW |
5 |
45,829,844 (GRCm39) |
critical splice donor site |
probably null |
|
|