Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
A |
T |
19: 43,807,869 (GRCm39) |
I837F |
probably damaging |
Het |
Acot3 |
A |
G |
12: 84,103,866 (GRCm39) |
Y225C |
probably benign |
Het |
Adam17 |
A |
G |
12: 21,378,056 (GRCm39) |
V710A |
probably damaging |
Het |
Ank3 |
A |
G |
10: 69,761,899 (GRCm39) |
|
probably benign |
Het |
Ankrd60 |
T |
A |
2: 173,410,610 (GRCm39) |
K303N |
possibly damaging |
Het |
Atp10b |
T |
A |
11: 43,094,024 (GRCm39) |
S523T |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,971,588 (GRCm39) |
V973A |
possibly damaging |
Het |
Ccdc24 |
C |
T |
4: 117,729,691 (GRCm39) |
W9* |
probably null |
Het |
Ccdc82 |
A |
G |
9: 13,281,891 (GRCm39) |
T439A |
probably benign |
Het |
Ccne2 |
C |
A |
4: 11,199,420 (GRCm39) |
Q274K |
probably benign |
Het |
Clec11a |
T |
C |
7: 43,956,189 (GRCm39) |
M1V |
probably null |
Het |
Col12a1 |
T |
A |
9: 79,541,017 (GRCm39) |
Y2370F |
probably benign |
Het |
Cyp4a32 |
C |
T |
4: 115,467,699 (GRCm39) |
H228Y |
probably benign |
Het |
Dchs2 |
G |
A |
3: 83,036,101 (GRCm39) |
G283S |
probably benign |
Het |
Dis3 |
T |
C |
14: 99,318,814 (GRCm39) |
T659A |
probably damaging |
Het |
Dock5 |
T |
C |
14: 68,060,071 (GRCm39) |
D456G |
possibly damaging |
Het |
Efr3b |
T |
A |
12: 4,033,409 (GRCm39) |
K249* |
probably null |
Het |
Emilin2 |
C |
T |
17: 71,581,539 (GRCm39) |
V396I |
probably benign |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fasn |
A |
T |
11: 120,706,735 (GRCm39) |
S947T |
probably benign |
Het |
Fryl |
C |
T |
5: 73,207,754 (GRCm39) |
C2472Y |
probably benign |
Het |
Gm3159 |
A |
T |
14: 4,398,488 (GRCm38) |
I60L |
probably benign |
Het |
Gm3402 |
A |
T |
5: 146,451,330 (GRCm39) |
N63Y |
probably damaging |
Het |
Gm49355 |
C |
T |
14: 12,296,641 (GRCm38) |
|
probably benign |
Het |
Grm2 |
A |
G |
9: 106,528,287 (GRCm39) |
L199P |
probably damaging |
Het |
Hck |
T |
A |
2: 152,992,904 (GRCm39) |
H470Q |
probably benign |
Het |
Hsd17b4 |
T |
C |
18: 50,299,981 (GRCm39) |
Y413H |
probably benign |
Het |
Ice1 |
A |
G |
13: 70,740,758 (GRCm39) |
F80L |
|
Het |
Ifrd1 |
G |
A |
12: 40,267,458 (GRCm39) |
P38S |
possibly damaging |
Het |
Itgad |
A |
G |
7: 127,788,479 (GRCm39) |
T431A |
probably benign |
Het |
Kcnd3 |
A |
T |
3: 105,566,003 (GRCm39) |
I395F |
probably damaging |
Het |
Kif20a |
A |
G |
18: 34,759,779 (GRCm39) |
E58G |
probably benign |
Het |
Kras |
A |
T |
6: 145,192,442 (GRCm39) |
D30E |
probably benign |
Het |
Lmbrd1 |
C |
T |
1: 24,724,593 (GRCm39) |
A59V |
probably damaging |
Het |
Lrrc20 |
T |
C |
10: 61,383,890 (GRCm39) |
L99P |
probably damaging |
Het |
Mfn2 |
T |
C |
4: 147,966,649 (GRCm39) |
D514G |
probably benign |
Het |
Myl2 |
A |
G |
5: 122,242,902 (GRCm39) |
E96G |
probably damaging |
Het |
Nppb |
T |
G |
4: 148,070,518 (GRCm39) |
L29R |
probably damaging |
Het |
Or51f1e |
C |
T |
7: 102,747,713 (GRCm39) |
A255V |
possibly damaging |
Het |
Or5ak22 |
A |
G |
2: 85,230,097 (GRCm39) |
V260A |
probably benign |
Het |
Pcdhb14 |
A |
G |
18: 37,581,281 (GRCm39) |
H129R |
probably damaging |
Het |
Pex11g |
T |
C |
8: 3,509,363 (GRCm39) |
N188S |
possibly damaging |
Het |
Pla2g3 |
A |
G |
11: 3,442,170 (GRCm39) |
D410G |
probably benign |
Het |
Pnma1 |
C |
A |
12: 84,194,232 (GRCm39) |
W157L |
probably benign |
Het |
Pofut2 |
A |
G |
10: 77,103,090 (GRCm39) |
Y362C |
probably damaging |
Het |
Ppp1r14c |
C |
A |
10: 3,373,567 (GRCm39) |
S126* |
probably null |
Het |
Rere |
T |
A |
4: 150,554,770 (GRCm39) |
V156D |
probably damaging |
Het |
Rsf1 |
CGGC |
CGGCGGCGGGGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Samd8 |
G |
A |
14: 21,830,227 (GRCm39) |
V281I |
probably benign |
Het |
Scarf1 |
A |
G |
11: 75,404,401 (GRCm39) |
|
probably benign |
Het |
Scgb2b27 |
A |
G |
7: 33,712,722 (GRCm39) |
L40P |
probably benign |
Het |
Sdk1 |
A |
T |
5: 142,147,708 (GRCm39) |
H1780L |
probably benign |
Het |
Slc10a6 |
T |
C |
5: 103,754,521 (GRCm39) |
T337A |
probably benign |
Het |
Slc44a4 |
A |
T |
17: 35,140,219 (GRCm39) |
D208V |
probably benign |
Het |
Slco1c1 |
G |
T |
6: 141,493,553 (GRCm39) |
C363F |
probably benign |
Het |
Smg5 |
T |
A |
3: 88,261,848 (GRCm39) |
L707Q |
probably damaging |
Het |
Supt5 |
A |
T |
7: 28,016,412 (GRCm39) |
D789E |
probably benign |
Het |
Tbcd |
A |
G |
11: 121,464,648 (GRCm39) |
Y561C |
probably damaging |
Het |
Tectb |
T |
C |
19: 55,183,097 (GRCm39) |
L316P |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,326 (GRCm39) |
T129A |
possibly damaging |
Het |
Tnpo3 |
T |
C |
6: 29,558,851 (GRCm39) |
H693R |
probably benign |
Het |
Trim54 |
T |
G |
5: 31,294,478 (GRCm39) |
D335E |
probably benign |
Het |
Tsr1 |
A |
G |
11: 74,790,126 (GRCm39) |
D107G |
probably benign |
Het |
Ttc41 |
A |
T |
10: 86,595,089 (GRCm39) |
E954D |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,538,595 (GRCm39) |
L34701P |
possibly damaging |
Het |
Vmn1r119 |
A |
C |
7: 20,746,034 (GRCm39) |
V116G |
probably damaging |
Het |
Vmn1r219 |
G |
A |
13: 23,346,769 (GRCm39) |
|
probably benign |
Het |
Zc3h12c |
T |
A |
9: 52,028,010 (GRCm39) |
M470L |
probably benign |
Het |
Zmynd8 |
T |
C |
2: 165,654,668 (GRCm39) |
K615E |
possibly damaging |
Het |
|
Other mutations in Psg27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Psg27
|
APN |
7 |
18,295,729 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00417:Psg27
|
APN |
7 |
18,295,842 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01344:Psg27
|
APN |
7 |
18,294,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Psg27
|
APN |
7 |
18,298,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02547:Psg27
|
APN |
7 |
18,294,553 (GRCm39) |
missense |
probably benign |
|
IGL02926:Psg27
|
APN |
7 |
18,291,054 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03074:Psg27
|
APN |
7 |
18,294,454 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03237:Psg27
|
APN |
7 |
18,294,417 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02796:Psg27
|
UTSW |
7 |
18,295,875 (GRCm39) |
missense |
probably benign |
0.08 |
R0437:Psg27
|
UTSW |
7 |
18,294,636 (GRCm39) |
splice site |
probably benign |
|
R0604:Psg27
|
UTSW |
7 |
18,290,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R1163:Psg27
|
UTSW |
7 |
18,299,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R2072:Psg27
|
UTSW |
7 |
18,298,934 (GRCm39) |
missense |
probably benign |
0.16 |
R2072:Psg27
|
UTSW |
7 |
18,294,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2073:Psg27
|
UTSW |
7 |
18,294,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Psg27
|
UTSW |
7 |
18,294,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2081:Psg27
|
UTSW |
7 |
18,290,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Psg27
|
UTSW |
7 |
18,301,036 (GRCm39) |
nonsense |
probably null |
|
R2866:Psg27
|
UTSW |
7 |
18,295,818 (GRCm39) |
missense |
probably benign |
|
R3783:Psg27
|
UTSW |
7 |
18,294,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Psg27
|
UTSW |
7 |
18,294,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R4463:Psg27
|
UTSW |
7 |
18,291,010 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5312:Psg27
|
UTSW |
7 |
18,290,958 (GRCm39) |
missense |
probably benign |
0.43 |
R5885:Psg27
|
UTSW |
7 |
18,295,711 (GRCm39) |
missense |
probably damaging |
0.96 |
R6087:Psg27
|
UTSW |
7 |
18,290,869 (GRCm39) |
missense |
probably benign |
0.05 |
R7011:Psg27
|
UTSW |
7 |
18,290,798 (GRCm39) |
missense |
probably benign |
0.00 |
R7198:Psg27
|
UTSW |
7 |
18,295,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Psg27
|
UTSW |
7 |
18,301,008 (GRCm39) |
missense |
probably benign |
0.20 |
R7964:Psg27
|
UTSW |
7 |
18,299,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R8398:Psg27
|
UTSW |
7 |
18,295,837 (GRCm39) |
missense |
probably benign |
0.29 |
R8472:Psg27
|
UTSW |
7 |
18,296,015 (GRCm39) |
missense |
probably benign |
0.18 |
R8818:Psg27
|
UTSW |
7 |
18,294,337 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Psg27
|
UTSW |
7 |
18,295,720 (GRCm39) |
nonsense |
probably null |
|
|