Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
T |
3: 121,930,630 (GRCm39) |
I1376F |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,488,129 (GRCm39) |
N673D |
possibly damaging |
Het |
Avil |
T |
C |
10: 126,845,867 (GRCm39) |
F372S |
probably damaging |
Het |
Bltp1 |
A |
T |
3: 37,102,749 (GRCm39) |
M4863L |
probably benign |
Het |
Bod1l |
T |
A |
5: 41,989,948 (GRCm39) |
E258D |
probably benign |
Het |
Chek1 |
T |
A |
9: 36,621,701 (GRCm39) |
H420L |
probably benign |
Het |
Cyfip1 |
A |
G |
7: 55,528,899 (GRCm39) |
I260M |
probably damaging |
Het |
Dclk1 |
G |
A |
3: 55,397,285 (GRCm39) |
V524I |
probably damaging |
Het |
Efr3b |
T |
C |
12: 4,042,965 (GRCm39) |
M102V |
probably benign |
Het |
Erc2 |
T |
A |
14: 27,863,326 (GRCm39) |
I517N |
probably damaging |
Het |
Fubp1 |
T |
C |
3: 151,926,190 (GRCm39) |
I305T |
probably damaging |
Het |
Galc |
T |
A |
12: 98,182,520 (GRCm39) |
D443V |
probably benign |
Het |
Galnt4 |
T |
A |
10: 98,945,892 (GRCm39) |
I539N |
probably damaging |
Het |
Gm17093 |
G |
T |
14: 44,758,986 (GRCm39) |
M169I |
unknown |
Het |
Htra1 |
T |
C |
7: 130,583,469 (GRCm39) |
F363S |
probably damaging |
Het |
Itprid1 |
A |
T |
6: 55,874,876 (GRCm39) |
K275N |
probably benign |
Het |
Klhdc8b |
G |
A |
9: 108,328,261 (GRCm39) |
P64S |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,614,130 (GRCm39) |
|
probably null |
Het |
Mettl21c |
T |
G |
1: 44,048,882 (GRCm39) |
K222Q |
probably damaging |
Het |
Mga |
A |
C |
2: 119,771,744 (GRCm39) |
M1535L |
possibly damaging |
Het |
Mov10 |
C |
T |
3: 104,708,828 (GRCm39) |
G395D |
probably damaging |
Het |
Ms4a10 |
C |
A |
19: 10,946,054 (GRCm39) |
A26S |
probably benign |
Het |
Mtcl3 |
A |
T |
10: 29,073,269 (GRCm39) |
M854L |
probably benign |
Het |
Naaladl1 |
A |
G |
19: 6,159,684 (GRCm39) |
N372D |
possibly damaging |
Het |
Optc |
T |
C |
1: 133,825,617 (GRCm39) |
D303G |
probably damaging |
Het |
Or4f52 |
A |
T |
2: 111,061,304 (GRCm39) |
I278N |
probably damaging |
Het |
Osmr |
C |
A |
15: 6,845,268 (GRCm39) |
V833L |
probably benign |
Het |
Phf14 |
A |
G |
6: 11,997,251 (GRCm39) |
|
probably null |
Het |
Pjvk |
A |
G |
2: 76,488,713 (GRCm39) |
I295V |
probably benign |
Het |
Plppr4 |
T |
A |
3: 117,119,513 (GRCm39) |
I299L |
possibly damaging |
Het |
Prkg1 |
A |
G |
19: 31,563,072 (GRCm39) |
S110P |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,555,744 (GRCm39) |
|
probably benign |
Het |
Rarb |
T |
G |
14: 16,443,820 (GRCm38) |
N156T |
possibly damaging |
Het |
Rgl3 |
A |
T |
9: 21,892,898 (GRCm39) |
|
probably null |
Het |
Ruvbl1 |
A |
C |
6: 88,460,097 (GRCm39) |
|
probably null |
Het |
S1pr1 |
G |
T |
3: 115,505,789 (GRCm39) |
C268* |
probably null |
Het |
Sbk3 |
T |
C |
7: 4,972,996 (GRCm39) |
D58G |
probably benign |
Het |
Smim8 |
TTTAATGAAGAGCT |
TT |
4: 34,771,261 (GRCm39) |
|
probably benign |
Het |
Tas2r119 |
T |
C |
15: 32,177,452 (GRCm39) |
L6P |
probably damaging |
Het |
Tcp11 |
A |
T |
17: 28,288,210 (GRCm39) |
F339L |
probably damaging |
Het |
Tdpoz8 |
A |
G |
3: 92,981,039 (GRCm39) |
Y19C |
probably damaging |
Het |
Tmprss5 |
T |
A |
9: 49,025,779 (GRCm39) |
|
probably null |
Het |
Trnau1ap |
A |
G |
4: 132,052,521 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
G |
A |
2: 121,038,873 (GRCm39) |
R1397* |
probably null |
Het |
Ubqln3 |
G |
A |
7: 103,790,674 (GRCm39) |
P472L |
probably benign |
Het |
Vmn2r13 |
T |
A |
5: 109,321,966 (GRCm39) |
M244L |
possibly damaging |
Het |
Zfp777 |
C |
T |
6: 48,014,522 (GRCm39) |
E395K |
probably damaging |
Het |
Zfyve27 |
A |
G |
19: 42,171,935 (GRCm39) |
S156G |
probably benign |
Het |
|
Other mutations in Scgb2b3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1664:Scgb2b3
|
UTSW |
7 |
31,058,464 (GRCm39) |
makesense |
probably null |
|
R1772:Scgb2b3
|
UTSW |
7 |
31,059,621 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3862:Scgb2b3
|
UTSW |
7 |
31,061,430 (GRCm39) |
critical splice donor site |
probably null |
|
R6433:Scgb2b3
|
UTSW |
7 |
31,058,492 (GRCm39) |
missense |
probably benign |
0.15 |
R7135:Scgb2b3
|
UTSW |
7 |
31,059,639 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7145:Scgb2b3
|
UTSW |
7 |
31,059,573 (GRCm39) |
missense |
probably benign |
0.00 |
R7553:Scgb2b3
|
UTSW |
7 |
31,059,673 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7908:Scgb2b3
|
UTSW |
7 |
31,061,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R8172:Scgb2b3
|
UTSW |
7 |
31,058,476 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8350:Scgb2b3
|
UTSW |
7 |
31,061,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Scgb2b3
|
UTSW |
7 |
31,059,528 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9371:Scgb2b3
|
UTSW |
7 |
31,059,642 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Scgb2b3
|
UTSW |
7 |
31,059,681 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Scgb2b3
|
UTSW |
7 |
31,059,592 (GRCm39) |
missense |
probably benign |
|
Z1186:Scgb2b3
|
UTSW |
7 |
31,058,546 (GRCm39) |
missense |
probably benign |
|
|