Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adad2 |
G |
A |
8: 120,342,502 (GRCm39) |
R380H |
probably damaging |
Het |
Akr1c12 |
C |
A |
13: 4,325,767 (GRCm39) |
D109Y |
possibly damaging |
Het |
Cacna1s |
A |
T |
1: 136,033,582 (GRCm39) |
M1020L |
possibly damaging |
Het |
Cbx8 |
C |
A |
11: 118,931,213 (GRCm39) |
R25L |
possibly damaging |
Het |
Ccdc87 |
A |
G |
19: 4,891,407 (GRCm39) |
Y633C |
probably benign |
Het |
Col4a4 |
C |
T |
1: 82,484,752 (GRCm39) |
S505N |
unknown |
Het |
Cr2 |
T |
A |
1: 194,839,810 (GRCm39) |
H539L |
probably damaging |
Het |
Cyp2b9 |
T |
A |
7: 25,872,999 (GRCm39) |
D47E |
probably benign |
Het |
Dnah3 |
A |
C |
7: 119,608,607 (GRCm39) |
M1784R |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,966,828 (GRCm39) |
L2520* |
probably null |
Het |
E2f2 |
A |
G |
4: 135,905,796 (GRCm39) |
E103G |
possibly damaging |
Het |
Eef1akmt3 |
T |
A |
10: 126,868,877 (GRCm39) |
H199L |
possibly damaging |
Het |
Faxc |
A |
T |
4: 21,993,376 (GRCm39) |
N340I |
possibly damaging |
Het |
Fer1l6 |
A |
T |
15: 58,497,026 (GRCm39) |
R1199* |
probably null |
Het |
Fer1l6 |
A |
G |
15: 58,509,855 (GRCm39) |
D1439G |
probably damaging |
Het |
Galnt5 |
G |
T |
2: 57,925,261 (GRCm39) |
W847C |
probably damaging |
Het |
Gbp2 |
G |
A |
3: 142,337,793 (GRCm39) |
S303N |
probably benign |
Het |
Glipr1l1 |
A |
T |
10: 111,896,332 (GRCm39) |
K40* |
probably null |
Het |
Gm4353 |
A |
C |
7: 115,683,134 (GRCm39) |
L149R |
possibly damaging |
Het |
Grk5 |
A |
G |
19: 61,078,380 (GRCm39) |
D479G |
probably damaging |
Het |
Gzmc |
T |
A |
14: 56,471,486 (GRCm39) |
|
probably null |
Het |
Hace1 |
T |
C |
10: 45,524,986 (GRCm39) |
Y251H |
probably benign |
Het |
Hhla1 |
G |
T |
15: 65,813,646 (GRCm39) |
P229T |
probably damaging |
Het |
Hspa1l |
C |
T |
17: 35,196,428 (GRCm39) |
Q156* |
probably null |
Het |
Igkv4-78 |
A |
T |
6: 69,036,683 (GRCm39) |
Y117N |
probably benign |
Het |
Ikzf3 |
C |
A |
11: 98,357,879 (GRCm39) |
R486L |
probably damaging |
Het |
Itpr1 |
C |
T |
6: 108,355,164 (GRCm39) |
T485M |
possibly damaging |
Het |
Kcnab3 |
T |
C |
11: 69,219,401 (GRCm39) |
Y131H |
probably benign |
Het |
Kcnu1 |
C |
T |
8: 26,422,362 (GRCm39) |
P209L |
probably benign |
Het |
Klk1b8 |
T |
A |
7: 43,448,094 (GRCm39) |
C39* |
probably null |
Het |
Mbtps1 |
A |
G |
8: 120,255,700 (GRCm39) |
L519P |
probably damaging |
Het |
Mgat4a |
A |
G |
1: 37,495,673 (GRCm39) |
I287T |
probably damaging |
Het |
Mindy2 |
T |
C |
9: 70,512,480 (GRCm39) |
E590G |
possibly damaging |
Het |
Mllt11 |
G |
T |
3: 95,127,602 (GRCm39) |
T56K |
probably benign |
Het |
Myo5b |
G |
A |
18: 74,875,249 (GRCm39) |
R1551H |
probably damaging |
Het |
Nmrk2 |
T |
C |
10: 81,036,796 (GRCm39) |
T16A |
possibly damaging |
Het |
Or2ab1 |
T |
A |
11: 58,488,831 (GRCm39) |
F203Y |
probably damaging |
Het |
Or7e170 |
G |
T |
9: 19,795,365 (GRCm39) |
P79T |
probably damaging |
Het |
Osbpl9 |
T |
C |
4: 109,013,899 (GRCm39) |
D65G |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,957,131 (GRCm39) |
K1079* |
probably null |
Het |
Plcb1 |
A |
G |
2: 135,212,486 (GRCm39) |
S1026G |
possibly damaging |
Het |
Pnrc2 |
A |
T |
4: 135,599,397 (GRCm39) |
H117Q |
probably benign |
Het |
Rpl12 |
G |
A |
2: 32,853,000 (GRCm39) |
E72K |
probably benign |
Het |
Sbf1 |
C |
T |
15: 89,177,679 (GRCm39) |
R1642H |
probably benign |
Het |
Sephs2 |
G |
A |
7: 126,873,118 (GRCm39) |
|
probably benign |
Het |
Slc35c2 |
A |
T |
2: 165,122,617 (GRCm39) |
L194H |
probably damaging |
Het |
Slfn4 |
T |
A |
11: 83,079,938 (GRCm39) |
Y150N |
probably damaging |
Het |
Srbd1 |
T |
C |
17: 86,292,723 (GRCm39) |
R949G |
probably damaging |
Het |
Urah |
T |
A |
7: 140,415,618 (GRCm39) |
S28T |
probably damaging |
Het |
Wdr62 |
A |
G |
7: 29,941,860 (GRCm39) |
S649P |
probably damaging |
Het |
Wnk1 |
C |
A |
6: 119,929,728 (GRCm39) |
G1263V |
probably damaging |
Het |
Zbtb4 |
C |
A |
11: 69,669,069 (GRCm39) |
D114E |
possibly damaging |
Het |
|
Other mutations in Ppfia2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Ppfia2
|
APN |
10 |
106,655,353 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01296:Ppfia2
|
APN |
10 |
106,694,068 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01385:Ppfia2
|
APN |
10 |
106,749,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01592:Ppfia2
|
APN |
10 |
106,671,909 (GRCm39) |
splice site |
probably benign |
|
IGL01899:Ppfia2
|
APN |
10 |
106,751,612 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02063:Ppfia2
|
APN |
10 |
106,740,706 (GRCm39) |
missense |
probably null |
0.83 |
IGL02143:Ppfia2
|
APN |
10 |
106,693,360 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:Ppfia2
|
APN |
10 |
106,636,646 (GRCm39) |
missense |
probably benign |
|
IGL02565:Ppfia2
|
APN |
10 |
106,699,247 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02573:Ppfia2
|
APN |
10 |
106,664,789 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02819:Ppfia2
|
APN |
10 |
106,742,255 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02974:Ppfia2
|
APN |
10 |
106,636,637 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03165:Ppfia2
|
APN |
10 |
106,603,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Ppfia2
|
APN |
10 |
106,732,368 (GRCm39) |
missense |
possibly damaging |
0.76 |
Colorless
|
UTSW |
10 |
106,749,455 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4458001:Ppfia2
|
UTSW |
10 |
106,763,708 (GRCm39) |
missense |
probably benign |
0.24 |
R0018:Ppfia2
|
UTSW |
10 |
106,678,647 (GRCm39) |
splice site |
probably benign |
|
R0018:Ppfia2
|
UTSW |
10 |
106,678,647 (GRCm39) |
splice site |
probably benign |
|
R0323:Ppfia2
|
UTSW |
10 |
106,732,281 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0391:Ppfia2
|
UTSW |
10 |
106,666,575 (GRCm39) |
splice site |
probably benign |
|
R0667:Ppfia2
|
UTSW |
10 |
106,749,555 (GRCm39) |
missense |
probably damaging |
0.97 |
R0782:Ppfia2
|
UTSW |
10 |
106,763,592 (GRCm39) |
missense |
probably benign |
0.32 |
R0905:Ppfia2
|
UTSW |
10 |
106,655,372 (GRCm39) |
missense |
probably benign |
0.43 |
R1401:Ppfia2
|
UTSW |
10 |
106,666,518 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1672:Ppfia2
|
UTSW |
10 |
106,666,429 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1723:Ppfia2
|
UTSW |
10 |
106,751,533 (GRCm39) |
splice site |
probably null |
|
R1780:Ppfia2
|
UTSW |
10 |
106,732,368 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1847:Ppfia2
|
UTSW |
10 |
106,763,571 (GRCm39) |
missense |
probably benign |
0.16 |
R2015:Ppfia2
|
UTSW |
10 |
106,310,538 (GRCm39) |
missense |
probably benign |
0.01 |
R2051:Ppfia2
|
UTSW |
10 |
106,673,160 (GRCm39) |
missense |
probably damaging |
0.98 |
R2061:Ppfia2
|
UTSW |
10 |
106,673,190 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2115:Ppfia2
|
UTSW |
10 |
106,597,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R2310:Ppfia2
|
UTSW |
10 |
106,690,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R2394:Ppfia2
|
UTSW |
10 |
106,655,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R2656:Ppfia2
|
UTSW |
10 |
106,701,268 (GRCm39) |
splice site |
probably null |
|
R3113:Ppfia2
|
UTSW |
10 |
106,742,256 (GRCm39) |
nonsense |
probably null |
|
R3968:Ppfia2
|
UTSW |
10 |
106,742,382 (GRCm39) |
missense |
probably damaging |
0.99 |
R3977:Ppfia2
|
UTSW |
10 |
106,666,490 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3978:Ppfia2
|
UTSW |
10 |
106,666,490 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3979:Ppfia2
|
UTSW |
10 |
106,666,490 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4567:Ppfia2
|
UTSW |
10 |
106,701,267 (GRCm39) |
splice site |
probably null |
|
R4632:Ppfia2
|
UTSW |
10 |
106,671,905 (GRCm39) |
splice site |
probably null |
|
R4718:Ppfia2
|
UTSW |
10 |
106,694,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Ppfia2
|
UTSW |
10 |
106,597,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Ppfia2
|
UTSW |
10 |
106,597,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Ppfia2
|
UTSW |
10 |
106,751,551 (GRCm39) |
missense |
probably benign |
0.01 |
R4841:Ppfia2
|
UTSW |
10 |
106,690,818 (GRCm39) |
missense |
probably benign |
0.04 |
R4842:Ppfia2
|
UTSW |
10 |
106,690,818 (GRCm39) |
missense |
probably benign |
0.04 |
R4914:Ppfia2
|
UTSW |
10 |
106,597,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Ppfia2
|
UTSW |
10 |
106,597,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Ppfia2
|
UTSW |
10 |
106,597,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Ppfia2
|
UTSW |
10 |
106,701,224 (GRCm39) |
nonsense |
probably null |
|
R5029:Ppfia2
|
UTSW |
10 |
106,693,304 (GRCm39) |
missense |
probably benign |
0.04 |
R5127:Ppfia2
|
UTSW |
10 |
106,671,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R5357:Ppfia2
|
UTSW |
10 |
106,740,708 (GRCm39) |
critical splice donor site |
probably null |
|
R5420:Ppfia2
|
UTSW |
10 |
106,671,562 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6030:Ppfia2
|
UTSW |
10 |
106,742,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Ppfia2
|
UTSW |
10 |
106,742,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Ppfia2
|
UTSW |
10 |
106,693,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Ppfia2
|
UTSW |
10 |
106,749,559 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6457:Ppfia2
|
UTSW |
10 |
106,729,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R6542:Ppfia2
|
UTSW |
10 |
106,671,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R6674:Ppfia2
|
UTSW |
10 |
106,763,633 (GRCm39) |
missense |
probably benign |
0.23 |
R6746:Ppfia2
|
UTSW |
10 |
106,742,319 (GRCm39) |
nonsense |
probably null |
|
R6992:Ppfia2
|
UTSW |
10 |
106,310,715 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7060:Ppfia2
|
UTSW |
10 |
106,597,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Ppfia2
|
UTSW |
10 |
106,693,356 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7453:Ppfia2
|
UTSW |
10 |
106,763,691 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7555:Ppfia2
|
UTSW |
10 |
106,763,687 (GRCm39) |
missense |
probably benign |
0.00 |
R7622:Ppfia2
|
UTSW |
10 |
106,666,520 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7637:Ppfia2
|
UTSW |
10 |
106,701,264 (GRCm39) |
critical splice donor site |
probably null |
|
R7866:Ppfia2
|
UTSW |
10 |
106,655,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R7897:Ppfia2
|
UTSW |
10 |
106,655,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R7937:Ppfia2
|
UTSW |
10 |
106,699,233 (GRCm39) |
missense |
probably benign |
0.30 |
R7938:Ppfia2
|
UTSW |
10 |
106,310,648 (GRCm39) |
missense |
probably damaging |
0.97 |
R8218:Ppfia2
|
UTSW |
10 |
106,699,236 (GRCm39) |
missense |
probably benign |
0.07 |
R8431:Ppfia2
|
UTSW |
10 |
106,671,952 (GRCm39) |
nonsense |
probably null |
|
R8806:Ppfia2
|
UTSW |
10 |
106,694,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R8984:Ppfia2
|
UTSW |
10 |
106,694,439 (GRCm39) |
intron |
probably benign |
|
R9008:Ppfia2
|
UTSW |
10 |
106,655,220 (GRCm39) |
missense |
probably benign |
0.00 |
R9014:Ppfia2
|
UTSW |
10 |
106,763,666 (GRCm39) |
missense |
probably benign |
0.05 |
R9182:Ppfia2
|
UTSW |
10 |
106,763,640 (GRCm39) |
missense |
probably benign |
0.39 |
R9201:Ppfia2
|
UTSW |
10 |
106,678,640 (GRCm39) |
critical splice donor site |
probably null |
|
R9249:Ppfia2
|
UTSW |
10 |
106,749,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R9620:Ppfia2
|
UTSW |
10 |
106,749,519 (GRCm39) |
missense |
|
|
R9710:Ppfia2
|
UTSW |
10 |
106,664,885 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Ppfia2
|
UTSW |
10 |
106,310,538 (GRCm39) |
missense |
probably benign |
0.06 |
X0022:Ppfia2
|
UTSW |
10 |
106,729,295 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ppfia2
|
UTSW |
10 |
106,310,506 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Ppfia2
|
UTSW |
10 |
106,742,416 (GRCm39) |
missense |
probably damaging |
1.00 |
|