Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,902,826 (GRCm39) |
K497E |
probably damaging |
Het |
4933413J09Rik |
A |
G |
14: 26,097,462 (GRCm39) |
|
noncoding transcript |
Het |
Aox1 |
A |
T |
1: 58,069,185 (GRCm39) |
I4F |
probably benign |
Het |
Arhgef5 |
A |
T |
6: 43,250,148 (GRCm39) |
N300Y |
probably damaging |
Het |
B530045E10Rik |
A |
G |
10: 99,257,983 (GRCm39) |
|
noncoding transcript |
Het |
Ccnb1 |
C |
G |
13: 100,918,283 (GRCm39) |
Q121H |
possibly damaging |
Het |
Cdh20 |
A |
G |
1: 104,875,073 (GRCm39) |
E285G |
probably damaging |
Het |
Cfap54 |
A |
T |
10: 92,722,249 (GRCm39) |
|
probably null |
Het |
Col6a3 |
A |
G |
1: 90,696,067 (GRCm39) |
C2667R |
unknown |
Het |
Cts8 |
C |
T |
13: 61,401,149 (GRCm39) |
V126M |
probably damaging |
Het |
Dag1 |
A |
T |
9: 108,084,771 (GRCm39) |
I790N |
possibly damaging |
Het |
Ddit4 |
A |
G |
10: 59,786,491 (GRCm39) |
I186T |
probably damaging |
Het |
Dnajc11 |
T |
A |
4: 152,054,271 (GRCm39) |
|
probably benign |
Het |
Farsa |
A |
G |
8: 85,595,593 (GRCm39) |
D495G |
probably benign |
Het |
Gm1527 |
T |
A |
3: 28,957,567 (GRCm39) |
I157N |
probably damaging |
Het |
Gm5773 |
T |
A |
3: 93,680,735 (GRCm39) |
W136R |
probably benign |
Het |
Hpse |
C |
A |
5: 100,867,403 (GRCm39) |
A20S |
unknown |
Het |
Igfn1 |
A |
G |
1: 135,887,634 (GRCm39) |
Y2477H |
probably damaging |
Het |
Kcnh5 |
A |
G |
12: 74,944,858 (GRCm39) |
V797A |
probably benign |
Het |
Kptn |
T |
A |
7: 15,859,710 (GRCm39) |
C311* |
probably null |
Het |
Lpcat2 |
A |
T |
8: 93,635,819 (GRCm39) |
N407I |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,375,503 (GRCm39) |
|
probably benign |
Het |
Ovol2 |
C |
T |
2: 144,159,780 (GRCm39) |
C120Y |
probably damaging |
Het |
Pcdhac2 |
G |
T |
18: 37,277,352 (GRCm39) |
E111* |
probably null |
Het |
Pknox1 |
C |
T |
17: 31,809,713 (GRCm39) |
P106S |
probably benign |
Het |
Plet1 |
C |
T |
9: 50,415,595 (GRCm39) |
T155I |
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,525,415 (GRCm39) |
I397N |
unknown |
Het |
Ranbp1 |
A |
G |
16: 18,065,151 (GRCm39) |
|
probably null |
Het |
Raver2 |
T |
C |
4: 100,960,182 (GRCm39) |
C221R |
probably damaging |
Het |
Reps1 |
A |
G |
10: 17,969,628 (GRCm39) |
T244A |
probably benign |
Het |
Slc22a16 |
G |
A |
10: 40,449,953 (GRCm39) |
V130I |
probably benign |
Het |
Stmnd1 |
G |
A |
13: 46,453,071 (GRCm39) |
S249N |
probably benign |
Het |
Styx |
A |
G |
14: 45,610,961 (GRCm39) |
|
probably null |
Het |
Sult1b1 |
T |
G |
5: 87,669,407 (GRCm39) |
N147T |
probably damaging |
Het |
Tbc1d2 |
G |
A |
4: 46,633,639 (GRCm39) |
|
probably benign |
Het |
Tm4sf1 |
T |
G |
3: 57,200,289 (GRCm39) |
I109L |
possibly damaging |
Het |
Ufl1 |
T |
C |
4: 25,256,010 (GRCm39) |
E423G |
probably benign |
Het |
Unc13c |
T |
C |
9: 73,840,654 (GRCm39) |
I66V |
probably benign |
Het |
Wfdc10 |
C |
T |
2: 164,499,060 (GRCm39) |
Q57* |
probably null |
Het |
Zeb1os1 |
T |
C |
18: 5,567,390 (GRCm39) |
|
noncoding transcript |
Het |
Zfp369 |
A |
T |
13: 65,426,847 (GRCm39) |
|
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 |
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 |
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 |
|