Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
G |
T |
11: 110,218,637 (GRCm39) |
N76K |
probably benign |
Het |
Adamts12 |
C |
T |
15: 11,215,710 (GRCm39) |
R244C |
probably damaging |
Het |
Atad2 |
A |
G |
15: 57,962,115 (GRCm39) |
S1143P |
probably benign |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
Cand1 |
A |
G |
10: 119,052,425 (GRCm39) |
S234P |
probably benign |
Het |
Cd200 |
T |
A |
16: 45,215,220 (GRCm39) |
I144L |
probably benign |
Het |
Cep76 |
A |
T |
18: 67,767,848 (GRCm39) |
L228Q |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,535,744 (GRCm39) |
L2584S |
probably damaging |
Het |
Col6a3 |
A |
C |
1: 90,755,823 (GRCm39) |
D155E |
probably damaging |
Het |
Col6a4 |
G |
A |
9: 105,907,158 (GRCm39) |
|
probably benign |
Het |
Dsg2 |
A |
C |
18: 20,706,556 (GRCm39) |
D24A |
possibly damaging |
Het |
Gm5901 |
G |
A |
7: 105,026,697 (GRCm39) |
S155N |
possibly damaging |
Het |
Hkdc1 |
T |
C |
10: 62,247,644 (GRCm39) |
|
probably benign |
Het |
Kansl1 |
A |
G |
11: 104,234,364 (GRCm39) |
V714A |
probably benign |
Het |
Kcnh1 |
T |
A |
1: 192,188,346 (GRCm39) |
S936T |
probably benign |
Het |
Klhdc3 |
A |
T |
17: 46,988,151 (GRCm39) |
F205I |
probably benign |
Het |
Krt31 |
T |
A |
11: 99,938,951 (GRCm39) |
H290L |
probably benign |
Het |
Lama2 |
T |
A |
10: 27,220,406 (GRCm39) |
|
probably null |
Het |
Mep1a |
T |
G |
17: 43,789,081 (GRCm39) |
D565A |
probably benign |
Het |
Mgme1 |
T |
A |
2: 144,120,907 (GRCm39) |
|
probably benign |
Het |
Mtf2 |
C |
T |
5: 108,252,369 (GRCm39) |
T409I |
probably damaging |
Het |
Mylk3 |
A |
G |
8: 86,081,794 (GRCm39) |
|
probably null |
Het |
Myo1c |
A |
G |
11: 75,559,338 (GRCm39) |
E650G |
probably damaging |
Het |
Nipbl |
A |
C |
15: 8,390,488 (GRCm39) |
D260E |
possibly damaging |
Het |
Nufip2 |
T |
A |
11: 77,582,839 (GRCm39) |
V251D |
possibly damaging |
Het |
Or2n1e |
C |
A |
17: 38,586,048 (GRCm39) |
P129T |
probably damaging |
Het |
Or4a2 |
T |
C |
2: 89,248,032 (GRCm39) |
I242V |
probably benign |
Het |
Or7g35 |
T |
A |
9: 19,496,743 (GRCm39) |
N303K |
probably benign |
Het |
Osm |
G |
T |
11: 4,189,918 (GRCm39) |
R234L |
possibly damaging |
Het |
Pabpc1 |
G |
A |
15: 36,598,275 (GRCm39) |
A515V |
probably benign |
Het |
Piwil1 |
T |
A |
5: 128,818,542 (GRCm39) |
|
probably null |
Het |
Pld1 |
A |
G |
3: 28,133,327 (GRCm39) |
|
probably null |
Het |
Plekhg3 |
C |
T |
12: 76,623,372 (GRCm39) |
R871C |
probably damaging |
Het |
Prmt3 |
A |
G |
7: 49,441,743 (GRCm39) |
Y240C |
probably damaging |
Het |
Prr36 |
G |
T |
8: 4,266,311 (GRCm39) |
|
probably benign |
Het |
Ptprd |
A |
G |
4: 75,875,583 (GRCm39) |
I908T |
probably damaging |
Het |
Sae1 |
A |
T |
7: 16,102,457 (GRCm39) |
N172K |
probably damaging |
Het |
Satb1 |
T |
G |
17: 52,089,889 (GRCm39) |
Q319H |
probably damaging |
Het |
Scart2 |
C |
G |
7: 139,841,450 (GRCm39) |
S251R |
possibly damaging |
Het |
Scn2a |
A |
T |
2: 65,582,340 (GRCm39) |
I1563F |
possibly damaging |
Het |
Scn3a |
C |
A |
2: 65,314,755 (GRCm39) |
R1102L |
probably null |
Het |
Serpinb9b |
T |
A |
13: 33,216,909 (GRCm39) |
L60* |
probably null |
Het |
Setd1a |
A |
G |
7: 127,385,765 (GRCm39) |
D281G |
probably damaging |
Het |
Slc8a1 |
C |
A |
17: 81,956,310 (GRCm39) |
V243F |
probably damaging |
Het |
Tgfbr3 |
A |
T |
5: 107,325,716 (GRCm39) |
H115Q |
probably benign |
Het |
Tiam1 |
C |
A |
16: 89,694,872 (GRCm39) |
S195I |
probably damaging |
Het |
Tjp2 |
A |
G |
19: 24,086,113 (GRCm39) |
V803A |
probably benign |
Het |
Ttc5 |
T |
A |
14: 51,003,415 (GRCm39) |
Q423L |
probably benign |
Het |
Tyk2 |
A |
C |
9: 21,020,167 (GRCm39) |
V997G |
probably damaging |
Het |
Uhrf1 |
T |
C |
17: 56,617,677 (GRCm39) |
V133A |
probably benign |
Het |
Vmn2r107 |
A |
C |
17: 20,575,916 (GRCm39) |
Y82S |
possibly damaging |
Het |
Vmn2r93 |
T |
C |
17: 18,546,503 (GRCm39) |
F792L |
probably damaging |
Het |
Vps13c |
G |
A |
9: 67,858,855 (GRCm39) |
W2768* |
probably null |
Het |
Zfp456 |
A |
T |
13: 67,514,861 (GRCm39) |
C282S |
probably benign |
Het |
Zhx1 |
T |
C |
15: 57,916,561 (GRCm39) |
N562D |
possibly damaging |
Het |
Zmynd15 |
G |
T |
11: 70,355,944 (GRCm39) |
G481C |
probably 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 |
|
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 |
|