Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
A |
G |
8: 124,709,195 (GRCm39) |
S120P |
probably benign |
Het |
Actr3b |
T |
A |
5: 26,036,743 (GRCm39) |
Y185* |
probably null |
Het |
Atg101 |
T |
A |
15: 101,188,382 (GRCm39) |
H162Q |
possibly damaging |
Het |
Btf3 |
T |
A |
13: 98,449,659 (GRCm39) |
Q109L |
possibly damaging |
Het |
Camk2d |
G |
A |
3: 126,574,091 (GRCm39) |
G166D |
probably damaging |
Het |
Capn7 |
T |
G |
14: 31,071,844 (GRCm39) |
|
probably null |
Het |
Cd209f |
A |
G |
8: 4,155,537 (GRCm39) |
V17A |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,385,656 (GRCm39) |
V2208A |
possibly damaging |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Comp |
T |
C |
8: 70,828,713 (GRCm39) |
C182R |
probably damaging |
Het |
Ctsl |
A |
G |
13: 64,516,840 (GRCm39) |
|
probably null |
Het |
Cyp3a44 |
G |
T |
5: 145,725,215 (GRCm39) |
Q329K |
probably damaging |
Het |
Dcpp1 |
A |
T |
17: 24,099,971 (GRCm39) |
|
probably null |
Het |
Dhx38 |
A |
G |
8: 110,280,891 (GRCm39) |
V831A |
probably damaging |
Het |
Dkk2 |
T |
C |
3: 131,791,858 (GRCm39) |
M22T |
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,346,742 (GRCm39) |
E2615K |
probably damaging |
Het |
Dpy19l3 |
A |
G |
7: 35,426,713 (GRCm39) |
|
probably null |
Het |
Gm12888 |
T |
G |
4: 121,176,655 (GRCm39) |
I49L |
probably benign |
Het |
Insyn2b |
C |
A |
11: 34,352,936 (GRCm39) |
S326Y |
probably benign |
Het |
Kif15 |
T |
A |
9: 122,815,252 (GRCm39) |
M194K |
probably damaging |
Het |
Mael |
G |
T |
1: 166,053,244 (GRCm39) |
Q254K |
probably benign |
Het |
Nek9 |
T |
C |
12: 85,361,322 (GRCm39) |
D461G |
probably benign |
Het |
Nlrp12 |
T |
C |
7: 3,281,825 (GRCm39) |
N819S |
probably benign |
Het |
Ntng1 |
T |
A |
3: 109,739,871 (GRCm39) |
N390Y |
probably damaging |
Het |
Or5g25 |
A |
G |
2: 85,478,434 (GRCm39) |
I77T |
probably benign |
Het |
P2ry14 |
C |
T |
3: 59,022,738 (GRCm39) |
V250I |
probably damaging |
Het |
Pcnx2 |
A |
T |
8: 126,485,987 (GRCm39) |
D1870E |
probably benign |
Het |
Phf2 |
T |
A |
13: 48,985,589 (GRCm39) |
K64* |
probably null |
Het |
Ppa2 |
A |
G |
3: 133,032,445 (GRCm39) |
T97A |
probably damaging |
Het |
Psd |
G |
A |
19: 46,313,088 (GRCm39) |
|
probably null |
Het |
Psg23 |
T |
A |
7: 18,348,668 (GRCm39) |
E46D |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rab11b |
A |
G |
17: 33,967,976 (GRCm39) |
Y74H |
probably damaging |
Het |
Rfc3 |
A |
T |
5: 151,568,383 (GRCm39) |
S194R |
probably benign |
Het |
Sema4d |
A |
T |
13: 51,864,037 (GRCm39) |
I414N |
probably damaging |
Het |
Serpinb1a |
A |
T |
13: 33,031,437 (GRCm39) |
D120E |
probably damaging |
Het |
Snai2 |
T |
A |
16: 14,524,861 (GRCm39) |
H122Q |
possibly damaging |
Het |
Spats2l |
T |
C |
1: 57,985,458 (GRCm39) |
S504P |
probably benign |
Het |
Sprr2j-ps |
T |
C |
3: 92,326,412 (GRCm39) |
S96P |
unknown |
Het |
Sspo |
G |
T |
6: 48,438,608 (GRCm39) |
V1559L |
probably benign |
Het |
Tas2r118 |
T |
G |
6: 23,969,912 (GRCm39) |
I50L |
possibly damaging |
Het |
Tdrd3 |
C |
T |
14: 87,743,788 (GRCm39) |
Q573* |
probably null |
Het |
Thoc2l |
T |
C |
5: 104,667,835 (GRCm39) |
S786P |
possibly damaging |
Het |
Tlnrd1 |
G |
A |
7: 83,532,062 (GRCm39) |
T123I |
probably benign |
Het |
Tmem214 |
T |
A |
5: 31,033,714 (GRCm39) |
L555H |
probably damaging |
Het |
Tmprss12 |
T |
A |
15: 100,183,117 (GRCm39) |
M153K |
probably benign |
Het |
Tmprss9 |
G |
A |
10: 80,725,268 (GRCm39) |
G410S |
probably damaging |
Het |
Trpm6 |
T |
A |
19: 18,803,116 (GRCm39) |
M853K |
probably damaging |
Het |
Vmn1r35 |
A |
G |
6: 66,655,929 (GRCm39) |
I247T |
possibly damaging |
Het |
Zcchc7 |
C |
A |
4: 44,931,059 (GRCm39) |
P404T |
probably damaging |
Het |
Zzef1 |
T |
C |
11: 72,763,465 (GRCm39) |
F1371L |
probably benign |
Het |
|
Other mutations in Phip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00809:Phip
|
APN |
9 |
82,753,356 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01510:Phip
|
APN |
9 |
82,795,924 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01916:Phip
|
APN |
9 |
82,772,522 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02068:Phip
|
APN |
9 |
82,827,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02089:Phip
|
APN |
9 |
82,753,372 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02121:Phip
|
APN |
9 |
82,775,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02132:Phip
|
APN |
9 |
82,763,394 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02146:Phip
|
APN |
9 |
82,763,771 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02282:Phip
|
APN |
9 |
82,795,743 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02341:Phip
|
APN |
9 |
82,814,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02342:Phip
|
APN |
9 |
82,768,745 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02470:Phip
|
APN |
9 |
82,772,507 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02585:Phip
|
APN |
9 |
82,785,241 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03271:Phip
|
APN |
9 |
82,766,877 (GRCm39) |
splice site |
probably benign |
|
3-1:Phip
|
UTSW |
9 |
82,768,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Phip
|
UTSW |
9 |
82,787,845 (GRCm39) |
splice site |
probably null |
|
R0102:Phip
|
UTSW |
9 |
82,787,845 (GRCm39) |
splice site |
probably null |
|
R0137:Phip
|
UTSW |
9 |
82,809,244 (GRCm39) |
splice site |
probably null |
|
R0268:Phip
|
UTSW |
9 |
82,753,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Phip
|
UTSW |
9 |
82,808,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Phip
|
UTSW |
9 |
82,808,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Phip
|
UTSW |
9 |
82,758,769 (GRCm39) |
splice site |
probably benign |
|
R0883:Phip
|
UTSW |
9 |
82,758,274 (GRCm39) |
missense |
probably benign |
0.01 |
R0885:Phip
|
UTSW |
9 |
82,757,448 (GRCm39) |
missense |
probably benign |
0.06 |
R1300:Phip
|
UTSW |
9 |
82,758,800 (GRCm39) |
missense |
probably benign |
0.00 |
R1434:Phip
|
UTSW |
9 |
82,841,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R1448:Phip
|
UTSW |
9 |
82,797,476 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1588:Phip
|
UTSW |
9 |
82,782,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Phip
|
UTSW |
9 |
82,753,502 (GRCm39) |
missense |
probably benign |
0.20 |
R1658:Phip
|
UTSW |
9 |
82,753,551 (GRCm39) |
missense |
probably benign |
|
R1688:Phip
|
UTSW |
9 |
82,753,710 (GRCm39) |
missense |
probably benign |
|
R1773:Phip
|
UTSW |
9 |
82,758,242 (GRCm39) |
missense |
probably benign |
|
R1865:Phip
|
UTSW |
9 |
82,827,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R1934:Phip
|
UTSW |
9 |
82,785,235 (GRCm39) |
missense |
probably benign |
0.11 |
R2070:Phip
|
UTSW |
9 |
82,757,352 (GRCm39) |
missense |
probably benign |
|
R2097:Phip
|
UTSW |
9 |
82,797,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2099:Phip
|
UTSW |
9 |
82,797,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2192:Phip
|
UTSW |
9 |
82,753,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R2402:Phip
|
UTSW |
9 |
82,757,358 (GRCm39) |
missense |
probably benign |
|
R2447:Phip
|
UTSW |
9 |
82,797,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R2504:Phip
|
UTSW |
9 |
82,797,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2507:Phip
|
UTSW |
9 |
82,797,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2508:Phip
|
UTSW |
9 |
82,797,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3706:Phip
|
UTSW |
9 |
82,782,796 (GRCm39) |
missense |
probably benign |
0.02 |
R3829:Phip
|
UTSW |
9 |
82,753,698 (GRCm39) |
missense |
probably benign |
|
R3846:Phip
|
UTSW |
9 |
82,758,179 (GRCm39) |
nonsense |
probably null |
|
R4301:Phip
|
UTSW |
9 |
82,841,766 (GRCm39) |
nonsense |
probably null |
|
R4366:Phip
|
UTSW |
9 |
82,782,922 (GRCm39) |
intron |
probably benign |
|
R4748:Phip
|
UTSW |
9 |
82,790,922 (GRCm39) |
missense |
probably benign |
0.01 |
R4895:Phip
|
UTSW |
9 |
82,841,648 (GRCm39) |
missense |
probably benign |
0.20 |
R5001:Phip
|
UTSW |
9 |
82,778,072 (GRCm39) |
splice site |
probably null |
|
R5094:Phip
|
UTSW |
9 |
82,753,897 (GRCm39) |
missense |
probably benign |
|
R5181:Phip
|
UTSW |
9 |
82,753,243 (GRCm39) |
utr 3 prime |
probably benign |
|
R5194:Phip
|
UTSW |
9 |
82,790,915 (GRCm39) |
missense |
probably benign |
0.03 |
R5291:Phip
|
UTSW |
9 |
82,827,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Phip
|
UTSW |
9 |
82,782,809 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5458:Phip
|
UTSW |
9 |
82,808,553 (GRCm39) |
missense |
probably benign |
0.40 |
R5704:Phip
|
UTSW |
9 |
82,753,408 (GRCm39) |
missense |
probably damaging |
0.97 |
R5866:Phip
|
UTSW |
9 |
82,772,203 (GRCm39) |
missense |
probably benign |
|
R5870:Phip
|
UTSW |
9 |
82,790,730 (GRCm39) |
splice site |
probably benign |
|
R5890:Phip
|
UTSW |
9 |
82,789,005 (GRCm39) |
missense |
probably benign |
0.00 |
R6232:Phip
|
UTSW |
9 |
82,785,234 (GRCm39) |
missense |
probably benign |
|
R6379:Phip
|
UTSW |
9 |
82,795,910 (GRCm39) |
missense |
probably damaging |
0.98 |
R6653:Phip
|
UTSW |
9 |
82,782,794 (GRCm39) |
nonsense |
probably null |
|
R7129:Phip
|
UTSW |
9 |
82,759,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R7290:Phip
|
UTSW |
9 |
82,753,346 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7598:Phip
|
UTSW |
9 |
82,787,711 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7632:Phip
|
UTSW |
9 |
82,785,243 (GRCm39) |
missense |
probably benign |
|
R7752:Phip
|
UTSW |
9 |
82,772,203 (GRCm39) |
missense |
probably benign |
|
R7827:Phip
|
UTSW |
9 |
82,790,886 (GRCm39) |
missense |
probably benign |
|
R7901:Phip
|
UTSW |
9 |
82,772,203 (GRCm39) |
missense |
probably benign |
|
R7960:Phip
|
UTSW |
9 |
82,775,401 (GRCm39) |
missense |
probably benign |
0.00 |
R8006:Phip
|
UTSW |
9 |
82,772,179 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8066:Phip
|
UTSW |
9 |
82,757,351 (GRCm39) |
missense |
probably benign |
0.05 |
R8080:Phip
|
UTSW |
9 |
82,769,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R8135:Phip
|
UTSW |
9 |
82,812,427 (GRCm39) |
missense |
probably benign |
0.09 |
R8347:Phip
|
UTSW |
9 |
82,790,816 (GRCm39) |
missense |
probably benign |
0.02 |
R8459:Phip
|
UTSW |
9 |
82,758,106 (GRCm39) |
missense |
probably benign |
|
R8705:Phip
|
UTSW |
9 |
82,775,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R8706:Phip
|
UTSW |
9 |
82,787,765 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8743:Phip
|
UTSW |
9 |
82,809,140 (GRCm39) |
missense |
probably benign |
0.18 |
R8801:Phip
|
UTSW |
9 |
82,758,305 (GRCm39) |
missense |
probably benign |
0.22 |
R8930:Phip
|
UTSW |
9 |
82,789,041 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8932:Phip
|
UTSW |
9 |
82,789,041 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8969:Phip
|
UTSW |
9 |
82,809,017 (GRCm39) |
intron |
probably benign |
|
R9064:Phip
|
UTSW |
9 |
82,753,540 (GRCm39) |
missense |
probably benign |
0.20 |
R9332:Phip
|
UTSW |
9 |
82,757,412 (GRCm39) |
missense |
probably damaging |
0.98 |
R9335:Phip
|
UTSW |
9 |
82,814,979 (GRCm39) |
missense |
probably benign |
0.03 |
R9520:Phip
|
UTSW |
9 |
82,753,437 (GRCm39) |
missense |
possibly damaging |
0.88 |
|