Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,219,945 (GRCm39) |
T831A |
possibly damaging |
Het |
Actg2 |
T |
A |
6: 83,503,829 (GRCm39) |
I72F |
probably damaging |
Het |
Add1 |
A |
G |
5: 34,774,030 (GRCm39) |
T80A |
probably benign |
Het |
Alpk2 |
G |
A |
18: 65,483,591 (GRCm39) |
T139M |
probably damaging |
Het |
Aplp2 |
C |
T |
9: 31,078,973 (GRCm39) |
R325H |
probably damaging |
Het |
Aptx |
G |
A |
4: 40,694,917 (GRCm39) |
P140S |
probably benign |
Het |
Carm1 |
A |
G |
9: 21,486,708 (GRCm39) |
|
probably null |
Het |
Carmil2 |
A |
T |
8: 106,424,025 (GRCm39) |
I1293F |
probably benign |
Het |
Cdh8 |
T |
C |
8: 100,127,495 (GRCm39) |
T39A |
probably benign |
Het |
Cimip3 |
T |
C |
17: 47,724,651 (GRCm39) |
T60A |
probably benign |
Het |
Col15a1 |
T |
A |
4: 47,245,868 (GRCm39) |
N206K |
possibly damaging |
Het |
Copg2 |
C |
T |
6: 30,873,591 (GRCm39) |
|
probably null |
Het |
Ctr9 |
T |
G |
7: 110,646,078 (GRCm39) |
I690S |
probably damaging |
Het |
Dcaf8 |
T |
G |
1: 172,016,602 (GRCm39) |
I463S |
possibly damaging |
Het |
Dcp1b |
G |
T |
6: 119,183,473 (GRCm39) |
A187S |
possibly damaging |
Het |
Ddo |
T |
A |
10: 40,508,935 (GRCm39) |
D58E |
possibly damaging |
Het |
Dkkl1 |
G |
T |
7: 44,857,157 (GRCm39) |
R137S |
probably damaging |
Het |
Dxo |
A |
G |
17: 35,056,718 (GRCm39) |
N115S |
probably benign |
Het |
Ep400 |
A |
T |
5: 110,856,781 (GRCm39) |
|
probably benign |
Het |
F11 |
A |
G |
8: 45,714,098 (GRCm39) |
V7A |
probably benign |
Het |
Fermt1 |
G |
T |
2: 132,781,438 (GRCm39) |
|
probably null |
Het |
Fign |
A |
T |
2: 63,810,143 (GRCm39) |
F376I |
probably benign |
Het |
Flg2 |
G |
T |
3: 93,109,082 (GRCm39) |
G370V |
probably damaging |
Het |
Fndc3a |
A |
T |
14: 72,793,715 (GRCm39) |
D953E |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,808,511 (GRCm39) |
H1610L |
probably benign |
Het |
Inpp4b |
G |
T |
8: 82,737,179 (GRCm39) |
W525C |
probably damaging |
Het |
Kremen1 |
CGGG |
CGGGGGG |
11: 5,151,791 (GRCm39) |
|
probably benign |
Het |
Lgi2 |
A |
G |
5: 52,695,307 (GRCm39) |
*543R |
probably null |
Het |
Lyn |
A |
G |
4: 3,745,542 (GRCm39) |
T114A |
probably benign |
Het |
Lynx1 |
A |
G |
15: 74,623,169 (GRCm39) |
Y88H |
probably damaging |
Het |
Map4 |
C |
A |
9: 109,863,770 (GRCm39) |
P332T |
possibly damaging |
Het |
Mapk8ip3 |
A |
T |
17: 25,133,677 (GRCm39) |
C250* |
probably null |
Het |
Metap1d |
A |
G |
2: 71,352,954 (GRCm39) |
H261R |
probably damaging |
Het |
Mfrp |
T |
C |
9: 44,013,835 (GRCm39) |
V115A |
probably benign |
Het |
Mtbp |
A |
G |
15: 55,440,932 (GRCm39) |
Y373C |
probably damaging |
Het |
Mtor |
C |
A |
4: 148,614,948 (GRCm39) |
R1628S |
possibly damaging |
Het |
Muc5b |
A |
G |
7: 141,412,813 (GRCm39) |
N1920D |
unknown |
Het |
Myo1d |
T |
A |
11: 80,670,543 (GRCm39) |
M26L |
probably benign |
Het |
Neb |
A |
C |
2: 52,100,843 (GRCm39) |
D643E |
probably damaging |
Het |
Nme1 |
A |
G |
11: 93,851,513 (GRCm39) |
F108L |
possibly damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,207 (GRCm39) |
S249P |
probably damaging |
Het |
Or8c15 |
G |
T |
9: 38,120,670 (GRCm39) |
C54F |
probably damaging |
Het |
Pan2 |
T |
A |
10: 128,140,326 (GRCm39) |
D82E |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,762,612 (GRCm39) |
D3695G |
unknown |
Het |
Pcnx4 |
A |
T |
12: 72,603,573 (GRCm39) |
|
probably null |
Het |
Plg |
A |
G |
17: 12,622,116 (GRCm39) |
T479A |
probably benign |
Het |
Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
Pramel32 |
T |
G |
4: 88,547,195 (GRCm39) |
M246L |
probably damaging |
Het |
Ptgis |
T |
C |
2: 167,049,196 (GRCm39) |
D372G |
probably damaging |
Het |
Ranbp3l |
A |
G |
15: 8,997,949 (GRCm39) |
T14A |
probably benign |
Het |
Rcc1l |
A |
T |
5: 134,195,508 (GRCm39) |
V230D |
probably damaging |
Het |
Reln |
T |
C |
5: 22,184,688 (GRCm39) |
D1609G |
possibly damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
G |
A |
7: 28,802,967 (GRCm39) |
L696F |
possibly damaging |
Het |
Sacs |
T |
A |
14: 61,440,529 (GRCm39) |
D858E |
probably benign |
Het |
Sec16a |
C |
T |
2: 26,329,037 (GRCm39) |
V993I |
probably benign |
Het |
Skint5 |
T |
A |
4: 113,487,616 (GRCm39) |
I901F |
unknown |
Het |
Slc17a3 |
A |
T |
13: 24,030,230 (GRCm39) |
I114F |
probably benign |
Het |
Slc17a7 |
T |
A |
7: 44,818,288 (GRCm39) |
L71Q |
probably damaging |
Het |
Slc43a2 |
T |
C |
11: 75,461,403 (GRCm39) |
S452P |
probably damaging |
Het |
Smarca4 |
A |
G |
9: 21,546,994 (GRCm39) |
N173S |
possibly damaging |
Het |
Tbc1d21 |
T |
C |
9: 58,270,195 (GRCm39) |
Y161C |
probably damaging |
Het |
Tpsab1 |
C |
A |
17: 25,564,081 (GRCm39) |
C94F |
probably damaging |
Het |
Ubr5 |
G |
A |
15: 38,002,563 (GRCm39) |
P1496L |
probably damaging |
Het |
Unc80 |
G |
T |
1: 66,710,767 (GRCm39) |
A2679S |
possibly damaging |
Het |
Vdac1 |
T |
A |
11: 52,274,904 (GRCm39) |
V184E |
probably damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,763,985 (GRCm39) |
S287R |
probably benign |
Het |
Vmn2r91 |
T |
C |
17: 18,356,048 (GRCm39) |
F572L |
probably benign |
Het |
Vps13b |
G |
A |
15: 35,884,701 (GRCm39) |
E3125K |
probably benign |
Het |
Ythdf3 |
A |
G |
3: 16,259,059 (GRCm39) |
N406S |
possibly damaging |
Het |
Zfp708 |
T |
C |
13: 67,219,251 (GRCm39) |
K158E |
probably damaging |
Het |
|
Other mutations in Gfra3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Gfra3
|
APN |
18 |
34,824,601 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01778:Gfra3
|
APN |
18 |
34,824,644 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02051:Gfra3
|
APN |
18 |
34,828,894 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0107:Gfra3
|
UTSW |
18 |
34,844,359 (GRCm39) |
missense |
probably benign |
0.04 |
R0573:Gfra3
|
UTSW |
18 |
34,824,668 (GRCm39) |
missense |
probably benign |
|
R1029:Gfra3
|
UTSW |
18 |
34,823,892 (GRCm39) |
missense |
probably benign |
0.01 |
R1870:Gfra3
|
UTSW |
18 |
34,844,373 (GRCm39) |
missense |
probably damaging |
0.97 |
R4689:Gfra3
|
UTSW |
18 |
34,823,640 (GRCm39) |
missense |
unknown |
|
R4801:Gfra3
|
UTSW |
18 |
34,853,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R4802:Gfra3
|
UTSW |
18 |
34,853,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Gfra3
|
UTSW |
18 |
34,844,304 (GRCm39) |
missense |
probably benign |
0.00 |
R5824:Gfra3
|
UTSW |
18 |
34,844,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R6111:Gfra3
|
UTSW |
18 |
34,823,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Gfra3
|
UTSW |
18 |
34,837,582 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6228:Gfra3
|
UTSW |
18 |
34,828,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Gfra3
|
UTSW |
18 |
34,828,864 (GRCm39) |
frame shift |
probably null |
|
R6759:Gfra3
|
UTSW |
18 |
34,828,926 (GRCm39) |
nonsense |
probably null |
|
R6781:Gfra3
|
UTSW |
18 |
34,844,375 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6894:Gfra3
|
UTSW |
18 |
34,828,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7021:Gfra3
|
UTSW |
18 |
34,823,933 (GRCm39) |
missense |
probably benign |
0.00 |
R7232:Gfra3
|
UTSW |
18 |
34,844,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Gfra3
|
UTSW |
18 |
34,828,884 (GRCm39) |
missense |
probably damaging |
0.99 |
R8830:Gfra3
|
UTSW |
18 |
34,844,189 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8987:Gfra3
|
UTSW |
18 |
34,823,879 (GRCm39) |
missense |
probably benign |
0.14 |
R9329:Gfra3
|
UTSW |
18 |
34,837,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Gfra3
|
UTSW |
18 |
34,837,591 (GRCm39) |
missense |
probably benign |
0.00 |
|