Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd6 |
A |
T |
14: 8,042,742 (GRCm38) |
T100S |
probably benign |
Het |
Adam6a |
T |
C |
12: 113,508,998 (GRCm39) |
I457T |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,246,996 (GRCm39) |
N863S |
probably benign |
Het |
Agk |
C |
A |
6: 40,353,168 (GRCm39) |
D177E |
probably benign |
Het |
Alg9 |
C |
T |
9: 50,699,500 (GRCm39) |
A209V |
probably damaging |
Het |
Arl6 |
A |
T |
16: 59,444,676 (GRCm39) |
I51K |
probably damaging |
Het |
Bpi |
A |
T |
2: 158,103,272 (GRCm39) |
H89L |
probably damaging |
Het |
C1qtnf1 |
T |
A |
11: 118,339,110 (GRCm39) |
F260Y |
probably benign |
Het |
Cblc |
T |
A |
7: 19,518,747 (GRCm39) |
D452V |
probably benign |
Het |
Ccar1 |
T |
C |
10: 62,612,473 (GRCm39) |
T231A |
probably benign |
Het |
Ccdc112 |
A |
G |
18: 46,420,499 (GRCm39) |
L417P |
probably damaging |
Het |
Ccdc34 |
G |
A |
2: 109,874,649 (GRCm39) |
R336Q |
possibly damaging |
Het |
CK137956 |
A |
G |
4: 127,844,829 (GRCm39) |
S305P |
probably benign |
Het |
Clip2 |
T |
C |
5: 134,531,969 (GRCm39) |
D612G |
probably damaging |
Het |
Col28a1 |
T |
C |
6: 8,059,360 (GRCm39) |
T692A |
probably benign |
Het |
Copg2 |
A |
T |
6: 30,793,676 (GRCm39) |
|
probably null |
Het |
Ctnna2 |
T |
A |
6: 76,950,774 (GRCm39) |
I566F |
possibly damaging |
Het |
Cux2 |
C |
T |
5: 121,999,389 (GRCm39) |
D1184N |
probably benign |
Het |
Dclk3 |
A |
G |
9: 111,297,422 (GRCm39) |
E322G |
probably benign |
Het |
Ddx41 |
A |
T |
13: 55,681,906 (GRCm39) |
|
probably null |
Het |
Dnaaf2 |
G |
A |
12: 69,243,559 (GRCm39) |
P107S |
probably damaging |
Het |
Eif2ak4 |
A |
G |
2: 118,261,428 (GRCm39) |
E578G |
probably damaging |
Het |
Exd1 |
A |
G |
2: 119,359,144 (GRCm39) |
|
probably benign |
Het |
Fat2 |
G |
A |
11: 55,173,583 (GRCm39) |
P2377S |
probably damaging |
Het |
Fbxl18 |
T |
C |
5: 142,858,214 (GRCm39) |
T741A |
probably benign |
Het |
Fmo4 |
T |
C |
1: 162,626,458 (GRCm39) |
T363A |
probably damaging |
Het |
Fsbp |
T |
C |
4: 11,584,006 (GRCm39) |
V235A |
probably benign |
Het |
Gm1110 |
T |
A |
9: 26,805,554 (GRCm39) |
H366L |
probably benign |
Het |
Gm43302 |
T |
C |
5: 105,438,846 (GRCm39) |
N14S |
probably damaging |
Het |
Gm5422 |
A |
G |
10: 31,124,764 (GRCm39) |
|
noncoding transcript |
Het |
Gm57858 |
A |
T |
3: 36,064,827 (GRCm39) |
C515* |
probably null |
Het |
Gpr21 |
A |
G |
2: 37,407,547 (GRCm39) |
E31G |
probably damaging |
Het |
Gucy1b2 |
G |
T |
14: 62,646,207 (GRCm39) |
N560K |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,553,085 (GRCm39) |
Q2535R |
probably benign |
Het |
Hnrnpm |
A |
T |
17: 33,883,598 (GRCm39) |
N264K |
probably damaging |
Het |
Hyal6 |
A |
T |
6: 24,734,723 (GRCm39) |
I219L |
possibly damaging |
Het |
Ifi211 |
A |
G |
1: 173,735,169 (GRCm39) |
S87P |
probably damaging |
Het |
Il17rb |
A |
T |
14: 29,718,797 (GRCm39) |
C428* |
probably null |
Het |
Iqca1 |
T |
C |
1: 89,973,348 (GRCm39) |
N808S |
probably benign |
Het |
Kcnu1 |
A |
G |
8: 26,408,470 (GRCm39) |
I94V |
probably benign |
Het |
Lrba |
A |
T |
3: 86,217,324 (GRCm39) |
E517V |
probably damaging |
Het |
Mcidas |
A |
G |
13: 113,130,515 (GRCm39) |
E37G |
possibly damaging |
Het |
Med23 |
T |
A |
10: 24,755,653 (GRCm39) |
F83L |
possibly damaging |
Het |
Micu2 |
T |
C |
14: 58,191,590 (GRCm39) |
|
probably null |
Het |
Mrgprx2 |
A |
T |
7: 48,132,282 (GRCm39) |
C179S |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,215,004 (GRCm39) |
T1236A |
probably damaging |
Het |
Myo7a |
A |
T |
7: 97,703,915 (GRCm39) |
V1946E |
possibly damaging |
Het |
Nek10 |
A |
T |
14: 14,885,122 (GRCm38) |
Y695F |
probably damaging |
Het |
Nr3c2 |
A |
T |
8: 77,636,422 (GRCm39) |
I508F |
possibly damaging |
Het |
Or11g27 |
T |
C |
14: 50,771,141 (GRCm39) |
S91P |
probably damaging |
Het |
Or14a260 |
A |
T |
7: 85,984,955 (GRCm39) |
Y216* |
probably null |
Het |
Or2ag13 |
T |
C |
7: 106,472,634 (GRCm39) |
I273V |
probably benign |
Het |
Or5w1b |
A |
T |
2: 87,476,233 (GRCm39) |
I78N |
probably damaging |
Het |
Or8k23 |
A |
T |
2: 86,186,530 (GRCm39) |
H65Q |
possibly damaging |
Het |
Or9s13 |
T |
C |
1: 92,548,471 (GRCm39) |
V281A |
probably benign |
Het |
Oxct1 |
T |
C |
15: 4,183,243 (GRCm39) |
S485P |
probably benign |
Het |
Oxt |
A |
G |
2: 130,418,572 (GRCm39) |
D61G |
probably damaging |
Het |
P2ry10 |
A |
C |
X: 106,146,241 (GRCm39) |
I59L |
probably damaging |
Het |
Parp11 |
A |
G |
6: 127,454,854 (GRCm39) |
N124S |
probably benign |
Het |
Pcdh7 |
T |
A |
5: 57,876,971 (GRCm39) |
N175K |
probably damaging |
Het |
Pdgfrb |
T |
A |
18: 61,194,566 (GRCm39) |
S114R |
probably benign |
Het |
Pfdn5 |
A |
G |
15: 102,234,956 (GRCm39) |
N54S |
possibly damaging |
Het |
Phc2 |
T |
A |
4: 128,617,378 (GRCm39) |
V468E |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,192,815 (GRCm39) |
T1605A |
probably damaging |
Het |
Pik3cb |
A |
T |
9: 98,987,632 (GRCm39) |
Y35* |
probably null |
Het |
Piwil2 |
A |
T |
14: 70,664,083 (GRCm39) |
M22K |
probably damaging |
Het |
Plag1 |
A |
G |
4: 3,904,889 (GRCm39) |
F101L |
probably damaging |
Het |
Pomt2 |
A |
G |
12: 87,158,173 (GRCm39) |
L680P |
possibly damaging |
Het |
Ppp1r36 |
A |
G |
12: 76,465,700 (GRCm39) |
|
probably null |
Het |
Prkag2 |
C |
T |
5: 25,076,052 (GRCm39) |
|
probably null |
Het |
Prkg1 |
T |
C |
19: 31,641,542 (GRCm39) |
D47G |
possibly damaging |
Het |
Prl6a1 |
G |
A |
13: 27,499,352 (GRCm39) |
G45D |
probably benign |
Het |
Rbm20 |
G |
A |
19: 53,847,859 (GRCm39) |
C1135Y |
probably damaging |
Het |
Recql5 |
A |
T |
11: 115,787,923 (GRCm39) |
N465K |
probably benign |
Het |
Rlig1 |
T |
G |
10: 100,419,820 (GRCm39) |
D58A |
probably damaging |
Het |
Rtcb |
A |
T |
10: 85,777,797 (GRCm39) |
I459N |
probably damaging |
Het |
Rtp3 |
A |
T |
9: 110,815,102 (GRCm39) |
|
probably benign |
Het |
Rundc3b |
T |
A |
5: 8,562,409 (GRCm39) |
|
probably null |
Het |
Scube3 |
A |
G |
17: 28,387,132 (GRCm39) |
T877A |
probably damaging |
Het |
Sh2d4a |
A |
T |
8: 68,799,394 (GRCm39) |
Q421L |
probably benign |
Het |
Siglec1 |
A |
T |
2: 130,925,277 (GRCm39) |
Y395N |
probably damaging |
Het |
Slc6a1 |
G |
T |
6: 114,284,731 (GRCm39) |
G263V |
probably damaging |
Het |
Slco1c1 |
T |
A |
6: 141,500,833 (GRCm39) |
F437L |
probably benign |
Het |
Slco3a1 |
G |
A |
7: 73,996,419 (GRCm39) |
A329V |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,983,201 (GRCm39) |
L504* |
probably null |
Het |
Spen |
A |
T |
4: 141,200,640 (GRCm39) |
N2662K |
probably damaging |
Het |
Sptb |
G |
C |
12: 76,679,246 (GRCm39) |
R70G |
possibly damaging |
Het |
Stk3 |
A |
G |
15: 35,072,644 (GRCm39) |
S136P |
probably damaging |
Het |
Synj1 |
A |
T |
16: 90,735,584 (GRCm39) |
F1456L |
probably damaging |
Het |
Tbx5 |
T |
C |
5: 119,979,971 (GRCm39) |
|
probably null |
Het |
Tchh |
G |
A |
3: 93,354,268 (GRCm39) |
R1236Q |
unknown |
Het |
Timd4 |
C |
A |
11: 46,710,857 (GRCm39) |
T253K |
possibly damaging |
Het |
Tmc6 |
A |
G |
11: 117,660,232 (GRCm39) |
Y669H |
probably damaging |
Het |
Tmem151a |
C |
T |
19: 5,132,966 (GRCm39) |
R80H |
probably benign |
Het |
Tpgs1 |
T |
C |
10: 79,511,722 (GRCm39) |
L288P |
probably damaging |
Het |
Trhde |
T |
C |
10: 114,334,698 (GRCm39) |
I659V |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,665,917 (GRCm39) |
Y896* |
probably null |
Het |
Ttc5 |
C |
A |
14: 51,019,007 (GRCm39) |
E37* |
probably null |
Het |
Uvrag |
A |
G |
7: 98,589,096 (GRCm39) |
|
probably null |
Het |
Vmn1r59 |
T |
A |
7: 5,457,283 (GRCm39) |
D159V |
probably damaging |
Het |
Vmn2r78 |
G |
A |
7: 86,604,287 (GRCm39) |
V822M |
possibly damaging |
Het |
Vnn1 |
C |
A |
10: 23,770,869 (GRCm39) |
Y32* |
probably null |
Het |
Wrn |
A |
G |
8: 33,726,432 (GRCm39) |
V1380A |
probably benign |
Het |
Zc3h14 |
A |
C |
12: 98,746,527 (GRCm39) |
S579R |
possibly damaging |
Het |
Zfp277 |
G |
A |
12: 40,367,217 (GRCm39) |
Q480* |
probably null |
Het |
Zfp456 |
G |
A |
13: 67,514,993 (GRCm39) |
Q238* |
probably null |
Het |
Zranb3 |
T |
A |
1: 128,019,638 (GRCm39) |
T35S |
probably benign |
Het |
|
Other mutations in Fgr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02201:Fgr
|
APN |
4 |
132,722,235 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03089:Fgr
|
APN |
4 |
132,713,577 (GRCm39) |
missense |
probably damaging |
0.96 |
R1760:Fgr
|
UTSW |
4 |
132,725,653 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1957:Fgr
|
UTSW |
4 |
132,725,673 (GRCm39) |
missense |
probably benign |
|
R2109:Fgr
|
UTSW |
4 |
132,725,786 (GRCm39) |
missense |
probably benign |
0.32 |
R2351:Fgr
|
UTSW |
4 |
132,724,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R2941:Fgr
|
UTSW |
4 |
132,725,734 (GRCm39) |
missense |
probably benign |
|
R3034:Fgr
|
UTSW |
4 |
132,725,807 (GRCm39) |
critical splice donor site |
probably null |
|
R4590:Fgr
|
UTSW |
4 |
132,722,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Fgr
|
UTSW |
4 |
132,714,602 (GRCm39) |
missense |
probably damaging |
0.99 |
R4847:Fgr
|
UTSW |
4 |
132,721,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R5294:Fgr
|
UTSW |
4 |
132,724,811 (GRCm39) |
missense |
probably benign |
0.01 |
R5384:Fgr
|
UTSW |
4 |
132,713,664 (GRCm39) |
critical splice donor site |
probably null |
|
R5388:Fgr
|
UTSW |
4 |
132,722,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Fgr
|
UTSW |
4 |
132,727,533 (GRCm39) |
missense |
probably benign |
0.13 |
R6947:Fgr
|
UTSW |
4 |
132,722,380 (GRCm39) |
critical splice donor site |
probably null |
|
R7651:Fgr
|
UTSW |
4 |
132,722,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Fgr
|
UTSW |
4 |
132,725,324 (GRCm39) |
missense |
probably benign |
|
R7921:Fgr
|
UTSW |
4 |
132,713,832 (GRCm39) |
splice site |
probably null |
|
R8011:Fgr
|
UTSW |
4 |
132,725,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8238:Fgr
|
UTSW |
4 |
132,724,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R8742:Fgr
|
UTSW |
4 |
132,724,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R8876:Fgr
|
UTSW |
4 |
132,726,071 (GRCm39) |
intron |
probably benign |
|
R8884:Fgr
|
UTSW |
4 |
132,713,609 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Fgr
|
UTSW |
4 |
132,727,481 (GRCm39) |
missense |
probably benign |
0.23 |
|