Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
A |
17: 48,347,951 (GRCm39) |
R118* |
probably null |
Het |
Acadsb |
T |
C |
7: 131,027,504 (GRCm39) |
V68A |
probably damaging |
Het |
Adgb |
T |
C |
10: 10,318,432 (GRCm39) |
R137G |
probably benign |
Het |
Adgrl3 |
C |
A |
5: 81,808,291 (GRCm39) |
N622K |
possibly damaging |
Het |
Ager |
C |
A |
17: 34,819,579 (GRCm39) |
P366T |
probably benign |
Het |
Barx2 |
C |
A |
9: 31,765,443 (GRCm39) |
W184L |
probably damaging |
Het |
Bckdha |
A |
C |
7: 25,341,144 (GRCm39) |
N72K |
probably benign |
Het |
Blm |
A |
T |
7: 80,162,867 (GRCm39) |
D161E |
probably damaging |
Het |
Ccdc121rt2 |
A |
T |
5: 112,598,757 (GRCm39) |
R435W |
probably damaging |
Het |
Cd96 |
G |
T |
16: 45,870,068 (GRCm39) |
T467N |
probably benign |
Het |
Cdk13 |
A |
T |
13: 17,978,444 (GRCm39) |
S265T |
unknown |
Het |
Col6a5 |
A |
C |
9: 105,766,142 (GRCm39) |
I1926S |
probably damaging |
Het |
Csgalnact2 |
A |
T |
6: 118,097,983 (GRCm39) |
V361D |
probably damaging |
Het |
Cstf1 |
T |
A |
2: 172,217,807 (GRCm39) |
M140K |
|
Het |
Ddx41 |
A |
T |
13: 55,683,424 (GRCm39) |
S128T |
probably benign |
Het |
Deaf1 |
A |
T |
7: 140,877,465 (GRCm39) |
V554D |
probably damaging |
Het |
Dido1 |
C |
T |
2: 180,303,293 (GRCm39) |
S1537N |
probably benign |
Het |
Dmwd |
T |
C |
7: 18,811,980 (GRCm39) |
S145P |
probably damaging |
Het |
Eftud2 |
A |
G |
11: 102,759,971 (GRCm39) |
S125P |
probably benign |
Het |
Gga1 |
A |
G |
15: 78,773,952 (GRCm39) |
D325G |
probably damaging |
Het |
Gm43518 |
T |
C |
5: 124,072,329 (GRCm39) |
|
probably null |
Het |
Got1l1 |
A |
T |
8: 27,690,889 (GRCm39) |
V53E |
probably damaging |
Het |
Helz2 |
A |
T |
2: 180,881,433 (GRCm39) |
C350S |
probably damaging |
Het |
Ipo7 |
T |
A |
7: 109,643,666 (GRCm39) |
F398I |
possibly damaging |
Het |
Itga11 |
A |
G |
9: 62,678,662 (GRCm39) |
N943S |
probably damaging |
Het |
Itpa |
T |
A |
2: 130,509,857 (GRCm39) |
|
probably null |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kbtbd4 |
A |
T |
2: 90,737,909 (GRCm39) |
N220Y |
possibly damaging |
Het |
Kdm5b |
T |
A |
1: 134,535,506 (GRCm39) |
F594L |
probably damaging |
Het |
Klhdc4 |
C |
T |
8: 122,524,684 (GRCm39) |
V446I |
probably benign |
Het |
Klk1b1 |
A |
G |
7: 43,620,668 (GRCm39) |
I253V |
possibly damaging |
Het |
Kynu |
T |
A |
2: 43,489,620 (GRCm39) |
M135K |
probably damaging |
Het |
Lgi1 |
T |
C |
19: 38,294,095 (GRCm39) |
I289T |
possibly damaging |
Het |
Lhx2 |
A |
G |
2: 38,250,045 (GRCm39) |
N288S |
probably damaging |
Het |
Lrp6 |
G |
C |
6: 134,488,169 (GRCm39) |
A309G |
probably damaging |
Het |
Map2 |
T |
A |
1: 66,452,098 (GRCm39) |
N329K |
probably benign |
Het |
Med15 |
G |
A |
16: 17,473,421 (GRCm39) |
P476L |
unknown |
Het |
Muc16 |
A |
T |
9: 18,555,846 (GRCm39) |
N3482K |
unknown |
Het |
Nemf |
A |
C |
12: 69,400,628 (GRCm39) |
V149G |
probably damaging |
Het |
Notch3 |
T |
C |
17: 32,370,521 (GRCm39) |
S706G |
probably benign |
Het |
Nphp4 |
T |
C |
4: 152,645,673 (GRCm39) |
V1227A |
possibly damaging |
Het |
Or1e31 |
A |
G |
11: 73,690,052 (GRCm39) |
F177S |
probably damaging |
Het |
Or2a52 |
A |
T |
6: 43,144,917 (GRCm39) |
R308S |
probably benign |
Het |
Or6c70 |
A |
G |
10: 129,710,488 (GRCm39) |
L46P |
probably damaging |
Het |
Pcdhgc3 |
T |
C |
18: 37,941,264 (GRCm39) |
V555A |
possibly damaging |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Ralgapa1 |
A |
C |
12: 55,723,351 (GRCm39) |
L1725R |
probably damaging |
Het |
Reln |
G |
T |
5: 22,130,198 (GRCm39) |
D2704E |
probably benign |
Het |
Sart3 |
C |
A |
5: 113,891,756 (GRCm39) |
E405D |
possibly damaging |
Het |
Scin |
A |
T |
12: 40,131,703 (GRCm39) |
L277* |
probably null |
Het |
Sec62 |
T |
A |
3: 30,868,383 (GRCm39) |
V204E |
probably benign |
Het |
Serpina3a |
T |
C |
12: 104,085,956 (GRCm39) |
I137T |
possibly damaging |
Het |
Sh3rf1 |
T |
C |
8: 61,825,613 (GRCm39) |
M536T |
probably benign |
Het |
Slc45a4 |
T |
C |
15: 73,457,953 (GRCm39) |
H532R |
probably damaging |
Het |
Svs5 |
A |
G |
2: 164,079,341 (GRCm39) |
F189L |
probably benign |
Het |
Synm |
T |
C |
7: 67,408,766 (GRCm39) |
D204G |
probably damaging |
Het |
Tmtc1 |
A |
T |
6: 148,147,215 (GRCm39) |
H827Q |
possibly damaging |
Het |
Tnfrsf25 |
T |
A |
4: 152,201,929 (GRCm39) |
C135* |
probably null |
Het |
Unc13b |
T |
G |
4: 43,095,847 (GRCm39) |
I85S |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,487,374 (GRCm39) |
Y3047* |
probably null |
Het |
Vmn1r75 |
T |
C |
7: 11,614,453 (GRCm39) |
S62P |
probably damaging |
Het |
Vps50 |
T |
C |
6: 3,536,884 (GRCm39) |
V285A |
probably benign |
Het |
Vwa5b1 |
T |
A |
4: 138,296,742 (GRCm39) |
D1095V |
probably benign |
Het |
Zdhhc21 |
T |
A |
4: 82,725,292 (GRCm39) |
D208V |
probably damaging |
Het |
Zfp422 |
A |
C |
6: 116,604,086 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Parp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02826:Parp2
|
APN |
14 |
51,052,872 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03022:Parp2
|
APN |
14 |
51,058,553 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03051:Parp2
|
APN |
14 |
51,056,805 (GRCm39) |
splice site |
probably benign |
|
R0110:Parp2
|
UTSW |
14 |
51,057,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0450:Parp2
|
UTSW |
14 |
51,057,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Parp2
|
UTSW |
14 |
51,057,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Parp2
|
UTSW |
14 |
51,056,732 (GRCm39) |
critical splice donor site |
probably null |
|
R1590:Parp2
|
UTSW |
14 |
51,048,001 (GRCm39) |
missense |
probably benign |
0.19 |
R1668:Parp2
|
UTSW |
14 |
51,058,313 (GRCm39) |
missense |
probably benign |
0.00 |
R1806:Parp2
|
UTSW |
14 |
51,056,836 (GRCm39) |
missense |
probably damaging |
0.99 |
R1846:Parp2
|
UTSW |
14 |
51,052,843 (GRCm39) |
nonsense |
probably null |
|
R2029:Parp2
|
UTSW |
14 |
51,047,543 (GRCm39) |
missense |
probably benign |
0.14 |
R2990:Parp2
|
UTSW |
14 |
51,054,457 (GRCm39) |
missense |
probably benign |
|
R3933:Parp2
|
UTSW |
14 |
51,056,844 (GRCm39) |
missense |
probably benign |
0.44 |
R4921:Parp2
|
UTSW |
14 |
51,056,725 (GRCm39) |
missense |
probably damaging |
0.99 |
R6406:Parp2
|
UTSW |
14 |
51,056,934 (GRCm39) |
missense |
probably benign |
|
R6799:Parp2
|
UTSW |
14 |
51,058,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R7105:Parp2
|
UTSW |
14 |
51,047,521 (GRCm39) |
frame shift |
probably null |
|
R7250:Parp2
|
UTSW |
14 |
51,054,801 (GRCm39) |
missense |
probably benign |
|
R7606:Parp2
|
UTSW |
14 |
51,057,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R8040:Parp2
|
UTSW |
14 |
51,047,630 (GRCm39) |
missense |
probably benign |
|
R8523:Parp2
|
UTSW |
14 |
51,057,247 (GRCm39) |
critical splice donor site |
probably null |
|
R9203:Parp2
|
UTSW |
14 |
51,056,850 (GRCm39) |
missense |
probably benign |
0.32 |
RF002:Parp2
|
UTSW |
14 |
51,054,843 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Parp2
|
UTSW |
14 |
51,054,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|