Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat3 |
G |
C |
17: 13,147,405 (GRCm39) |
P204R |
probably damaging |
Het |
Aldh3b1 |
A |
G |
19: 3,968,803 (GRCm39) |
I250T |
possibly damaging |
Het |
Ankrd11 |
C |
T |
8: 123,622,718 (GRCm39) |
R378K |
probably damaging |
Het |
Arap1 |
G |
A |
7: 101,057,324 (GRCm39) |
R1355Q |
possibly damaging |
Het |
Arhgef19 |
T |
C |
4: 140,976,603 (GRCm39) |
V455A |
probably damaging |
Het |
BC051019 |
T |
C |
7: 109,315,286 (GRCm39) |
E323G |
probably damaging |
Het |
Bzw2 |
T |
C |
12: 36,184,943 (GRCm39) |
N2S |
possibly damaging |
Het |
Calm3 |
G |
C |
7: 16,651,398 (GRCm39) |
F66L |
probably damaging |
Het |
Cemip2 |
T |
A |
19: 21,770,323 (GRCm39) |
S104T |
probably benign |
Het |
Cep170 |
A |
T |
1: 176,597,377 (GRCm39) |
C389S |
probably benign |
Het |
Clhc1 |
C |
T |
11: 29,510,533 (GRCm39) |
Q195* |
probably null |
Het |
Cttnbp2 |
A |
G |
6: 18,434,808 (GRCm39) |
L350P |
probably benign |
Het |
Cyp7a1 |
T |
C |
4: 6,271,238 (GRCm39) |
E306G |
possibly damaging |
Het |
Ddx25 |
T |
C |
9: 35,465,864 (GRCm39) |
N119S |
possibly damaging |
Het |
Ephx2 |
G |
T |
14: 66,322,441 (GRCm39) |
|
probably benign |
Het |
Ern2 |
C |
T |
7: 121,769,363 (GRCm39) |
A888T |
probably benign |
Het |
Fbln2 |
A |
T |
6: 91,246,072 (GRCm39) |
I973F |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,202,095 (GRCm39) |
I1259M |
probably damaging |
Het |
Glis1 |
A |
G |
4: 107,421,060 (GRCm39) |
H92R |
probably benign |
Het |
Gm13283 |
A |
C |
4: 88,679,516 (GRCm39) |
D169A |
probably benign |
Het |
Gpr61 |
A |
G |
3: 108,057,470 (GRCm39) |
L397P |
probably benign |
Het |
H4c11 |
T |
A |
13: 21,919,369 (GRCm39) |
I35N |
probably damaging |
Het |
Hip1 |
A |
T |
5: 135,460,297 (GRCm39) |
|
probably benign |
Het |
Hmgcs2 |
C |
T |
3: 98,203,557 (GRCm39) |
A222V |
probably damaging |
Het |
Ifna2 |
G |
A |
4: 88,601,712 (GRCm39) |
T102I |
probably benign |
Het |
Kat6b |
T |
C |
14: 21,674,995 (GRCm39) |
S387P |
probably damaging |
Het |
Ldlr |
G |
A |
9: 21,643,108 (GRCm39) |
V45M |
probably damaging |
Het |
Mc3r |
A |
T |
2: 172,091,515 (GRCm39) |
I246F |
possibly damaging |
Het |
Mug1 |
G |
C |
6: 121,861,296 (GRCm39) |
A1306P |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,368,020 (GRCm39) |
E260G |
probably benign |
Het |
Naa16 |
A |
G |
14: 79,582,395 (GRCm39) |
Y565H |
probably damaging |
Het |
Ndufaf7 |
A |
G |
17: 79,244,950 (GRCm39) |
Y23C |
possibly damaging |
Het |
Nop58 |
G |
A |
1: 59,731,549 (GRCm39) |
|
probably null |
Het |
Or6c33 |
A |
T |
10: 129,853,769 (GRCm39) |
T180S |
possibly damaging |
Het |
Or6c88 |
A |
T |
10: 129,406,550 (GRCm39) |
T9S |
probably benign |
Het |
Or7g19 |
T |
A |
9: 18,855,920 (GRCm39) |
|
probably benign |
Het |
Pcdh8 |
G |
A |
14: 80,006,971 (GRCm39) |
Q531* |
probably null |
Het |
Pik3c2g |
A |
G |
6: 139,821,093 (GRCm39) |
T297A |
probably benign |
Het |
Poc1b |
T |
C |
10: 99,028,861 (GRCm39) |
|
probably null |
Het |
Prb1c |
G |
A |
6: 132,338,897 (GRCm39) |
P107L |
|
Het |
Prokr2 |
A |
G |
2: 132,215,996 (GRCm39) |
V155A |
possibly damaging |
Het |
Rce1 |
C |
T |
19: 4,674,094 (GRCm39) |
|
probably benign |
Het |
Rnf148 |
A |
T |
6: 23,654,704 (GRCm39) |
N97K |
possibly damaging |
Het |
Setbp1 |
A |
G |
18: 78,899,723 (GRCm39) |
S1315P |
probably benign |
Het |
Sgcz |
A |
G |
8: 38,107,140 (GRCm39) |
V124A |
probably damaging |
Het |
Slc25a2 |
C |
A |
18: 37,771,089 (GRCm39) |
G147C |
probably damaging |
Het |
Slc28a2b |
C |
A |
2: 122,348,983 (GRCm39) |
P303Q |
|
Het |
Sod2 |
T |
C |
17: 13,227,193 (GRCm39) |
L49P |
probably damaging |
Het |
Tbc1d12 |
T |
C |
19: 38,854,098 (GRCm39) |
V260A |
probably benign |
Het |
Tcte2 |
C |
A |
17: 13,933,410 (GRCm39) |
|
probably benign |
Het |
Tenm3 |
T |
C |
8: 48,688,637 (GRCm39) |
T2317A |
probably damaging |
Het |
Tfcp2 |
T |
C |
15: 100,402,298 (GRCm39) |
I500V |
possibly damaging |
Het |
Trav14-3 |
C |
A |
14: 54,001,112 (GRCm39) |
Q108K |
probably damaging |
Het |
Trbv14 |
T |
C |
6: 41,112,364 (GRCm39) |
Y54H |
probably damaging |
Het |
Trpm3 |
T |
A |
19: 22,744,034 (GRCm39) |
V337E |
probably damaging |
Het |
Tsbp1 |
T |
C |
17: 34,659,328 (GRCm39) |
|
probably benign |
Het |
Uox |
A |
T |
3: 146,318,047 (GRCm39) |
I14F |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,065,421 (GRCm39) |
V1249A |
probably benign |
Het |
Zfp511 |
T |
C |
7: 139,617,194 (GRCm39) |
Y97H |
probably damaging |
Het |
Zfp536 |
G |
T |
7: 37,268,721 (GRCm39) |
Q232K |
probably benign |
Het |
Zng1 |
T |
G |
19: 24,932,780 (GRCm39) |
K84N |
probably damaging |
Het |
|
Other mutations in Carmil1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Carmil1
|
APN |
13 |
24,295,821 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00392:Carmil1
|
APN |
13 |
24,278,474 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00943:Carmil1
|
APN |
13 |
24,295,869 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01375:Carmil1
|
APN |
13 |
24,278,454 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02043:Carmil1
|
APN |
13 |
24,208,299 (GRCm39) |
unclassified |
probably benign |
|
IGL02122:Carmil1
|
APN |
13 |
24,220,541 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02178:Carmil1
|
APN |
13 |
24,278,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02264:Carmil1
|
APN |
13 |
24,259,699 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02269:Carmil1
|
APN |
13 |
24,339,393 (GRCm39) |
nonsense |
probably null |
|
IGL02546:Carmil1
|
APN |
13 |
24,299,482 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02740:Carmil1
|
APN |
13 |
24,278,501 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02876:Carmil1
|
APN |
13 |
24,338,651 (GRCm39) |
unclassified |
probably benign |
|
IGL02976:Carmil1
|
APN |
13 |
24,276,534 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03012:Carmil1
|
APN |
13 |
24,220,355 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03107:Carmil1
|
APN |
13 |
24,278,438 (GRCm39) |
missense |
probably damaging |
0.99 |
H8562:Carmil1
|
UTSW |
13 |
24,248,630 (GRCm39) |
missense |
probably benign |
0.00 |
R0085:Carmil1
|
UTSW |
13 |
24,209,850 (GRCm39) |
missense |
probably benign |
|
R0119:Carmil1
|
UTSW |
13 |
24,266,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R0166:Carmil1
|
UTSW |
13 |
24,283,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0299:Carmil1
|
UTSW |
13 |
24,266,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R0304:Carmil1
|
UTSW |
13 |
24,323,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R0335:Carmil1
|
UTSW |
13 |
24,257,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Carmil1
|
UTSW |
13 |
24,266,003 (GRCm39) |
missense |
probably damaging |
0.98 |
R0462:Carmil1
|
UTSW |
13 |
24,206,494 (GRCm39) |
missense |
probably benign |
0.01 |
R1203:Carmil1
|
UTSW |
13 |
24,282,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R1540:Carmil1
|
UTSW |
13 |
24,283,037 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1730:Carmil1
|
UTSW |
13 |
24,225,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Carmil1
|
UTSW |
13 |
24,357,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R1831:Carmil1
|
UTSW |
13 |
24,348,862 (GRCm39) |
missense |
probably benign |
0.00 |
R1893:Carmil1
|
UTSW |
13 |
24,208,446 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2099:Carmil1
|
UTSW |
13 |
24,357,650 (GRCm39) |
missense |
probably benign |
0.00 |
R2153:Carmil1
|
UTSW |
13 |
24,325,656 (GRCm39) |
missense |
probably damaging |
0.97 |
R2296:Carmil1
|
UTSW |
13 |
24,299,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Carmil1
|
UTSW |
13 |
24,229,051 (GRCm39) |
synonymous |
silent |
|
R2872:Carmil1
|
UTSW |
13 |
24,229,051 (GRCm39) |
synonymous |
silent |
|
R3113:Carmil1
|
UTSW |
13 |
24,253,740 (GRCm39) |
missense |
probably benign |
0.22 |
R3508:Carmil1
|
UTSW |
13 |
24,203,659 (GRCm39) |
utr 3 prime |
probably benign |
|
R3780:Carmil1
|
UTSW |
13 |
24,321,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R3954:Carmil1
|
UTSW |
13 |
24,197,390 (GRCm39) |
missense |
probably benign |
0.00 |
R4027:Carmil1
|
UTSW |
13 |
24,251,206 (GRCm39) |
splice site |
probably benign |
|
R4086:Carmil1
|
UTSW |
13 |
24,208,444 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4647:Carmil1
|
UTSW |
13 |
24,321,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Carmil1
|
UTSW |
13 |
24,325,659 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4792:Carmil1
|
UTSW |
13 |
24,251,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5012:Carmil1
|
UTSW |
13 |
24,208,403 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5166:Carmil1
|
UTSW |
13 |
24,338,966 (GRCm39) |
critical splice donor site |
probably null |
|
R5199:Carmil1
|
UTSW |
13 |
24,295,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Carmil1
|
UTSW |
13 |
24,209,929 (GRCm39) |
splice site |
probably null |
|
R5472:Carmil1
|
UTSW |
13 |
24,339,454 (GRCm39) |
missense |
probably damaging |
0.97 |
R5478:Carmil1
|
UTSW |
13 |
24,296,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Carmil1
|
UTSW |
13 |
24,339,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Carmil1
|
UTSW |
13 |
24,460,520 (GRCm39) |
missense |
probably benign |
|
R5789:Carmil1
|
UTSW |
13 |
24,305,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5794:Carmil1
|
UTSW |
13 |
24,276,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Carmil1
|
UTSW |
13 |
24,253,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6127:Carmil1
|
UTSW |
13 |
24,220,335 (GRCm39) |
missense |
probably benign |
0.03 |
R6128:Carmil1
|
UTSW |
13 |
24,197,177 (GRCm39) |
nonsense |
probably null |
|
R6403:Carmil1
|
UTSW |
13 |
24,265,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Carmil1
|
UTSW |
13 |
24,220,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R6451:Carmil1
|
UTSW |
13 |
24,276,541 (GRCm39) |
nonsense |
probably null |
|
R6684:Carmil1
|
UTSW |
13 |
24,206,525 (GRCm39) |
missense |
unknown |
|
R6891:Carmil1
|
UTSW |
13 |
24,325,706 (GRCm39) |
missense |
probably benign |
0.13 |
R6902:Carmil1
|
UTSW |
13 |
24,299,528 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6924:Carmil1
|
UTSW |
13 |
24,259,667 (GRCm39) |
nonsense |
probably null |
|
R6946:Carmil1
|
UTSW |
13 |
24,299,528 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7038:Carmil1
|
UTSW |
13 |
24,323,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Carmil1
|
UTSW |
13 |
24,204,052 (GRCm39) |
missense |
probably benign |
0.00 |
R7282:Carmil1
|
UTSW |
13 |
24,197,387 (GRCm39) |
missense |
probably benign |
|
R7286:Carmil1
|
UTSW |
13 |
24,197,377 (GRCm39) |
missense |
probably damaging |
0.96 |
R7397:Carmil1
|
UTSW |
13 |
24,228,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R7412:Carmil1
|
UTSW |
13 |
24,282,793 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7611:Carmil1
|
UTSW |
13 |
24,197,315 (GRCm39) |
missense |
probably benign |
0.30 |
R7642:Carmil1
|
UTSW |
13 |
24,251,189 (GRCm39) |
missense |
probably benign |
0.12 |
R7827:Carmil1
|
UTSW |
13 |
24,220,421 (GRCm39) |
missense |
probably benign |
0.00 |
R7890:Carmil1
|
UTSW |
13 |
24,197,215 (GRCm39) |
missense |
|
|
R8014:Carmil1
|
UTSW |
13 |
24,220,304 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8068:Carmil1
|
UTSW |
13 |
24,259,711 (GRCm39) |
missense |
probably benign |
0.00 |
R8214:Carmil1
|
UTSW |
13 |
24,228,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R8247:Carmil1
|
UTSW |
13 |
24,282,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Carmil1
|
UTSW |
13 |
24,220,562 (GRCm39) |
missense |
probably benign |
|
R8318:Carmil1
|
UTSW |
13 |
24,220,442 (GRCm39) |
missense |
probably benign |
|
R8361:Carmil1
|
UTSW |
13 |
24,251,113 (GRCm39) |
critical splice donor site |
probably null |
|
R8469:Carmil1
|
UTSW |
13 |
24,296,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8558:Carmil1
|
UTSW |
13 |
24,209,863 (GRCm39) |
missense |
probably benign |
|
R8698:Carmil1
|
UTSW |
13 |
24,220,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Carmil1
|
UTSW |
13 |
24,220,568 (GRCm39) |
missense |
probably benign |
0.16 |
R8836:Carmil1
|
UTSW |
13 |
24,339,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Carmil1
|
UTSW |
13 |
24,325,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R8932:Carmil1
|
UTSW |
13 |
24,197,179 (GRCm39) |
missense |
|
|
R9004:Carmil1
|
UTSW |
13 |
24,225,662 (GRCm39) |
missense |
probably damaging |
0.98 |
R9041:Carmil1
|
UTSW |
13 |
24,282,793 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9103:Carmil1
|
UTSW |
13 |
24,295,836 (GRCm39) |
missense |
probably benign |
0.01 |
R9224:Carmil1
|
UTSW |
13 |
24,292,512 (GRCm39) |
missense |
probably damaging |
0.98 |
R9428:Carmil1
|
UTSW |
13 |
24,295,834 (GRCm39) |
nonsense |
probably null |
|
R9460:Carmil1
|
UTSW |
13 |
24,253,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R9502:Carmil1
|
UTSW |
13 |
24,323,357 (GRCm39) |
missense |
probably benign |
|
R9548:Carmil1
|
UTSW |
13 |
24,460,516 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Carmil1
|
UTSW |
13 |
24,283,026 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1088:Carmil1
|
UTSW |
13 |
24,228,165 (GRCm39) |
nonsense |
probably null |
|
|