Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833439L19Rik |
C |
T |
13: 54,712,033 (GRCm39) |
|
probably benign |
Het |
Abcb8 |
T |
A |
5: 24,611,422 (GRCm39) |
N470K |
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,223,329 (GRCm39) |
N1037Y |
probably damaging |
Het |
Adcy3 |
T |
C |
12: 4,256,986 (GRCm39) |
|
probably benign |
Het |
Ankrd35 |
A |
G |
3: 96,597,524 (GRCm39) |
D983G |
possibly damaging |
Het |
Asf1a |
A |
G |
10: 53,483,920 (GRCm39) |
T118A |
probably benign |
Het |
Atp2a3 |
T |
C |
11: 72,868,033 (GRCm39) |
Y389H |
probably damaging |
Het |
Atp5f1b |
T |
C |
10: 127,919,821 (GRCm39) |
I63T |
probably damaging |
Het |
C2cd5 |
A |
G |
6: 143,028,946 (GRCm39) |
Y98H |
probably benign |
Het |
Caprin2 |
A |
G |
6: 148,749,756 (GRCm39) |
V518A |
probably damaging |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Clcn2 |
C |
A |
16: 20,528,006 (GRCm39) |
E487* |
probably null |
Het |
Cog6 |
T |
A |
3: 52,916,966 (GRCm39) |
K184M |
probably damaging |
Het |
Cpn1 |
A |
G |
19: 43,956,907 (GRCm39) |
Y286H |
probably damaging |
Het |
Cpne9 |
A |
T |
6: 113,277,624 (GRCm39) |
S448C |
probably damaging |
Het |
Csnk2a1 |
G |
T |
2: 152,116,005 (GRCm39) |
|
probably benign |
Het |
Cys1 |
T |
C |
12: 24,717,169 (GRCm39) |
E132G |
possibly damaging |
Het |
Depdc7 |
T |
C |
2: 104,555,071 (GRCm39) |
M280V |
probably benign |
Het |
Fhad1 |
C |
T |
4: 141,646,069 (GRCm39) |
D298N |
probably benign |
Het |
Golga1 |
T |
A |
2: 38,929,090 (GRCm39) |
N318Y |
probably null |
Het |
Hsd3b6 |
A |
G |
3: 98,718,262 (GRCm39) |
V34A |
probably benign |
Het |
Krt9 |
A |
G |
11: 100,082,346 (GRCm39) |
I193T |
probably damaging |
Het |
Lama4 |
A |
T |
10: 38,902,565 (GRCm39) |
I180F |
possibly damaging |
Het |
Lamc1 |
T |
C |
1: 153,126,407 (GRCm39) |
T458A |
probably damaging |
Het |
Lin28b |
A |
T |
10: 45,346,155 (GRCm39) |
M1K |
probably null |
Het |
Myo16 |
T |
C |
8: 10,372,600 (GRCm39) |
C100R |
probably damaging |
Het |
Nt5c3 |
A |
T |
6: 56,860,718 (GRCm39) |
M279K |
probably damaging |
Het |
Rpl6 |
A |
G |
5: 121,345,264 (GRCm39) |
|
probably benign |
Het |
Rpn2 |
G |
T |
2: 157,158,130 (GRCm39) |
|
probably null |
Het |
Rspry1 |
T |
C |
8: 95,380,884 (GRCm39) |
V396A |
probably benign |
Het |
Serpina3i |
C |
T |
12: 104,234,761 (GRCm39) |
T364I |
probably damaging |
Het |
Shprh |
A |
G |
10: 11,030,509 (GRCm39) |
K242R |
possibly damaging |
Het |
Slit3 |
A |
G |
11: 35,062,417 (GRCm39) |
N72S |
possibly damaging |
Het |
Syt17 |
G |
A |
7: 118,009,143 (GRCm39) |
|
probably benign |
Het |
Tatdn3 |
C |
A |
1: 190,787,541 (GRCm39) |
A114S |
probably benign |
Het |
Tjp2 |
A |
G |
19: 24,091,469 (GRCm39) |
V564A |
probably damaging |
Het |
Tmem117 |
T |
C |
15: 94,777,253 (GRCm39) |
|
probably benign |
Het |
Tnfrsf8 |
T |
C |
4: 144,995,703 (GRCm39) |
E452G |
probably damaging |
Het |
Tns1 |
T |
C |
1: 73,976,407 (GRCm39) |
D1147G |
probably damaging |
Het |
Traf6 |
T |
C |
2: 101,515,134 (GRCm39) |
S97P |
probably damaging |
Het |
Ttc28 |
A |
T |
5: 111,414,449 (GRCm39) |
E1321D |
probably benign |
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 |
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 |
R6237:Ppfia2
|
UTSW |
10 |
106,749,455 (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 |
|