Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,918,101 (GRCm39) |
I1534M |
probably benign |
Het |
Acad11 |
G |
A |
9: 104,003,785 (GRCm39) |
A626T |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,119,174 (GRCm39) |
N3560K |
probably benign |
Het |
Aldh3a2 |
C |
T |
11: 61,144,470 (GRCm39) |
V363I |
probably benign |
Het |
Anks1b |
A |
G |
10: 89,912,843 (GRCm39) |
T289A |
probably benign |
Het |
Atp11a |
A |
G |
8: 12,862,340 (GRCm39) |
N64S |
probably damaging |
Het |
Atp11c |
T |
C |
X: 59,282,072 (GRCm39) |
|
probably null |
Het |
Cd101 |
T |
C |
3: 100,919,329 (GRCm39) |
H591R |
probably damaging |
Het |
Cd36 |
C |
T |
5: 18,002,120 (GRCm39) |
V294I |
probably benign |
Het |
Cfap47 |
C |
A |
X: 78,532,251 (GRCm39) |
L842F |
probably damaging |
Het |
Cgref1 |
T |
C |
5: 31,090,929 (GRCm39) |
E295G |
probably benign |
Het |
Cit |
A |
G |
5: 116,083,901 (GRCm39) |
M787V |
probably benign |
Het |
Clcn6 |
G |
A |
4: 148,097,235 (GRCm39) |
P611S |
possibly damaging |
Het |
Clec12a |
A |
C |
6: 129,327,384 (GRCm39) |
M1L |
probably damaging |
Het |
Cmtm6 |
C |
T |
9: 114,575,573 (GRCm39) |
R161W |
probably damaging |
Het |
Colec10 |
G |
T |
15: 54,325,658 (GRCm39) |
V163L |
probably damaging |
Het |
Coq8b |
A |
G |
7: 26,956,907 (GRCm39) |
Y520C |
probably damaging |
Het |
Ctsll3 |
C |
A |
13: 60,948,821 (GRCm39) |
E45* |
probably null |
Het |
Dsg3 |
A |
G |
18: 20,669,975 (GRCm39) |
E663G |
possibly damaging |
Het |
Dst |
G |
A |
1: 34,231,293 (GRCm39) |
R2962H |
probably benign |
Het |
Etnk2 |
T |
C |
1: 133,300,995 (GRCm39) |
I254T |
probably damaging |
Het |
Fbxo36 |
T |
C |
1: 84,858,835 (GRCm39) |
I40T |
probably damaging |
Het |
Fgd2 |
G |
A |
17: 29,597,383 (GRCm39) |
V568M |
probably damaging |
Het |
Fmn1 |
T |
C |
2: 113,356,207 (GRCm39) |
Y883H |
possibly damaging |
Het |
Fpr-rs4 |
A |
T |
17: 18,242,589 (GRCm39) |
T199S |
possibly damaging |
Het |
Gm12789 |
A |
G |
4: 101,846,131 (GRCm39) |
K131E |
probably benign |
Het |
Gm17641 |
C |
A |
3: 68,777,448 (GRCm39) |
|
silent |
Het |
Gm6665 |
G |
T |
18: 31,953,340 (GRCm39) |
R43S |
probably damaging |
Het |
Gzmc |
T |
A |
14: 56,470,203 (GRCm39) |
H98L |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,491,528 (GRCm39) |
E75V |
probably damaging |
Het |
Herc2 |
G |
T |
7: 55,796,417 (GRCm39) |
V1930L |
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Htr6 |
A |
T |
4: 138,801,776 (GRCm39) |
C99* |
probably null |
Het |
Lgals2 |
C |
T |
15: 78,736,511 (GRCm39) |
M16I |
probably benign |
Het |
Lrrc8c |
A |
G |
5: 105,756,090 (GRCm39) |
N622D |
probably damaging |
Het |
Myo15a |
A |
T |
11: 60,383,791 (GRCm39) |
I1613F |
possibly damaging |
Het |
Oacyl |
C |
T |
18: 65,875,280 (GRCm39) |
R455C |
probably benign |
Het |
Or13c25 |
A |
T |
4: 52,911,397 (GRCm39) |
Y132* |
probably null |
Het |
Or5ac21 |
T |
A |
16: 59,123,766 (GRCm39) |
N84K |
probably benign |
Het |
Or5bh3 |
T |
C |
X: 49,098,872 (GRCm39) |
T81A |
possibly damaging |
Het |
Orm3 |
A |
G |
4: 63,275,146 (GRCm39) |
|
probably null |
Het |
Phf2 |
G |
C |
13: 48,985,579 (GRCm39) |
T67S |
unknown |
Het |
Phf2 |
A |
G |
13: 48,957,079 (GRCm39) |
L1096P |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,937,720 (GRCm39) |
F992L |
probably benign |
Het |
Ppp2r5e |
C |
G |
12: 75,516,341 (GRCm39) |
A239P |
probably damaging |
Het |
Pramel11 |
A |
G |
4: 143,622,263 (GRCm39) |
M364T |
probably benign |
Het |
Prmt7 |
A |
G |
8: 106,964,014 (GRCm39) |
T303A |
probably benign |
Het |
Prpf4b |
A |
T |
13: 35,078,426 (GRCm39) |
I679F |
possibly damaging |
Het |
Psd4 |
T |
A |
2: 24,293,292 (GRCm39) |
M719K |
probably benign |
Het |
Ranbp9 |
A |
T |
13: 43,578,593 (GRCm39) |
M160K |
probably benign |
Het |
Rfc1 |
A |
G |
5: 65,434,706 (GRCm39) |
Y687H |
probably damaging |
Het |
Rimbp2 |
T |
C |
5: 128,883,423 (GRCm39) |
K119R |
probably damaging |
Het |
Rnf113a1 |
T |
C |
X: 36,455,046 (GRCm39) |
M1T |
probably null |
Het |
Rnf40 |
A |
C |
7: 127,195,506 (GRCm39) |
K511Q |
possibly damaging |
Het |
Ryr2 |
T |
A |
13: 11,800,029 (GRCm39) |
|
probably null |
Het |
Scrib |
A |
T |
15: 75,937,011 (GRCm39) |
V365E |
probably damaging |
Het |
Slc6a17 |
A |
G |
3: 107,379,443 (GRCm39) |
V575A |
possibly damaging |
Het |
Spta1 |
A |
G |
1: 174,067,732 (GRCm39) |
N2053S |
possibly damaging |
Het |
Ssbp2 |
G |
A |
13: 91,790,511 (GRCm39) |
|
probably null |
Het |
Stab1 |
G |
T |
14: 30,882,456 (GRCm39) |
N460K |
probably benign |
Het |
Tbc1d9 |
T |
A |
8: 83,992,787 (GRCm39) |
C964S |
probably benign |
Het |
Tmed11 |
A |
G |
5: 108,927,680 (GRCm39) |
|
probably null |
Het |
Tmem191 |
C |
A |
16: 17,095,984 (GRCm39) |
R285S |
probably damaging |
Het |
Tpr |
T |
C |
1: 150,312,552 (GRCm39) |
S1917P |
probably benign |
Het |
Vill |
A |
T |
9: 118,892,440 (GRCm39) |
H357L |
probably benign |
Het |
Vmn1r229 |
A |
G |
17: 21,035,051 (GRCm39) |
T99A |
probably benign |
Het |
Vmn2r14 |
A |
G |
5: 109,369,283 (GRCm39) |
S97P |
probably damaging |
Het |
Wasf2 |
G |
T |
4: 132,917,483 (GRCm39) |
R194L |
unknown |
Het |
|
Other mutations in Pigt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03076:Pigt
|
APN |
2 |
164,339,585 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R1548:Pigt
|
UTSW |
2 |
164,343,439 (GRCm39) |
missense |
probably benign |
0.37 |
R1605:Pigt
|
UTSW |
2 |
164,349,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R3712:Pigt
|
UTSW |
2 |
164,343,565 (GRCm39) |
missense |
probably benign |
0.00 |
R3848:Pigt
|
UTSW |
2 |
164,340,500 (GRCm39) |
critical splice donor site |
probably benign |
|
R4672:Pigt
|
UTSW |
2 |
164,339,498 (GRCm39) |
unclassified |
probably benign |
|
R4719:Pigt
|
UTSW |
2 |
164,343,544 (GRCm39) |
missense |
probably damaging |
0.98 |
R5481:Pigt
|
UTSW |
2 |
164,348,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Pigt
|
UTSW |
2 |
164,343,482 (GRCm39) |
nonsense |
probably null |
|
R5570:Pigt
|
UTSW |
2 |
164,343,482 (GRCm39) |
nonsense |
probably null |
|
R5998:Pigt
|
UTSW |
2 |
164,349,374 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6112:Pigt
|
UTSW |
2 |
164,348,365 (GRCm39) |
nonsense |
probably null |
|
R6816:Pigt
|
UTSW |
2 |
164,343,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Pigt
|
UTSW |
2 |
164,349,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R7037:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R7197:Pigt
|
UTSW |
2 |
164,344,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R7288:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R7449:Pigt
|
UTSW |
2 |
164,344,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7822:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R7926:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R8005:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R8019:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R8330:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R8675:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R8893:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R8968:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9155:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9334:Pigt
|
UTSW |
2 |
164,349,420 (GRCm39) |
makesense |
probably null |
|
R9386:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9418:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9426:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9558:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9637:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
R9676:Pigt
|
UTSW |
2 |
164,341,589 (GRCm39) |
frame shift |
probably null |
|
|