Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
G |
A |
6: 92,808,972 (GRCm39) |
V100I |
unknown |
Het |
Acta2 |
G |
T |
19: 34,229,207 (GRCm39) |
Q61K |
probably damaging |
Het |
Adamts20 |
T |
G |
15: 94,258,490 (GRCm39) |
D357A |
probably damaging |
Het |
Adcy4 |
A |
G |
14: 56,009,452 (GRCm39) |
F798S |
probably benign |
Het |
Aldh16a1 |
A |
G |
7: 44,791,438 (GRCm39) |
V779A |
probably benign |
Het |
Arid1b |
C |
A |
17: 5,387,103 (GRCm39) |
P1466T |
probably benign |
Het |
B3gnt2 |
T |
C |
11: 22,787,002 (GRCm39) |
E62G |
probably damaging |
Het |
Bcan |
A |
C |
3: 87,904,582 (GRCm39) |
V58G |
probably damaging |
Het |
Bhlhe41 |
T |
C |
6: 145,810,339 (GRCm39) |
Q66R |
probably damaging |
Het |
Cdh6 |
G |
A |
15: 13,044,847 (GRCm39) |
T425I |
probably damaging |
Het |
Ciao2b |
C |
T |
8: 105,367,599 (GRCm39) |
|
probably null |
Het |
Csmd2 |
A |
G |
4: 128,457,195 (GRCm39) |
Y3554C |
probably damaging |
Het |
Csmd3 |
T |
A |
15: 48,321,024 (GRCm39) |
H262L |
possibly damaging |
Het |
Dgcr8 |
A |
G |
16: 18,098,500 (GRCm39) |
F334S |
probably damaging |
Het |
Dipk1c |
T |
C |
18: 84,757,617 (GRCm39) |
S234P |
probably benign |
Het |
Dsg1c |
A |
G |
18: 20,410,022 (GRCm39) |
T497A |
probably benign |
Het |
Dsp |
T |
C |
13: 38,381,502 (GRCm39) |
V2749A |
possibly damaging |
Het |
Esr1 |
A |
G |
10: 4,916,270 (GRCm39) |
N486D |
unknown |
Het |
Fbn2 |
T |
C |
18: 58,287,021 (GRCm39) |
T213A |
probably damaging |
Het |
Fbxo41 |
T |
A |
6: 85,461,663 (GRCm39) |
E15V |
probably damaging |
Het |
Fga |
G |
A |
3: 82,938,188 (GRCm39) |
A188T |
possibly damaging |
Het |
Frk |
C |
T |
10: 34,423,402 (GRCm39) |
S160F |
possibly damaging |
Het |
Gm4559 |
CTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAACAGCAGGGCTTGCAACAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCT |
CTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAACAGCAGGGCTTGCAACAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCT |
7: 141,827,553 (GRCm39) |
|
probably benign |
Het |
Gss |
T |
C |
2: 155,406,686 (GRCm39) |
Y432C |
probably damaging |
Het |
Ifi27l2b |
A |
T |
12: 103,423,298 (GRCm39) |
F5I |
unknown |
Het |
Insm1 |
T |
A |
2: 146,065,346 (GRCm39) |
Y387* |
probably null |
Het |
Klf12 |
T |
G |
14: 100,260,172 (GRCm39) |
I186L |
probably benign |
Het |
Klrg1 |
C |
T |
6: 122,248,342 (GRCm39) |
V186I |
probably benign |
Het |
Loxl3 |
G |
T |
6: 83,025,629 (GRCm39) |
W329L |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,835,595 (GRCm39) |
V1759E |
probably benign |
Het |
Mlph |
G |
A |
1: 90,870,609 (GRCm39) |
V507I |
probably benign |
Het |
Mroh8 |
G |
A |
2: 157,075,086 (GRCm39) |
T470M |
probably damaging |
Het |
Nampt |
T |
C |
12: 32,888,373 (GRCm39) |
Y175H |
possibly damaging |
Het |
Nedd4l |
A |
G |
18: 65,288,346 (GRCm39) |
E2G |
probably damaging |
Het |
Nrxn1 |
A |
G |
17: 91,009,393 (GRCm39) |
|
probably benign |
Het |
Optc |
A |
G |
1: 133,832,819 (GRCm39) |
S94P |
possibly damaging |
Het |
Or8k33 |
A |
G |
2: 86,383,727 (GRCm39) |
V247A |
probably benign |
Het |
Oxtr |
T |
A |
6: 112,466,873 (GRCm39) |
|
probably benign |
Het |
Pramel30 |
A |
G |
4: 144,059,438 (GRCm39) |
Y383C |
probably benign |
Het |
Psmc3ip |
T |
C |
11: 100,984,617 (GRCm39) |
N76S |
probably benign |
Het |
Reln |
T |
A |
5: 22,155,854 (GRCm39) |
M2213L |
possibly damaging |
Het |
Rock1 |
T |
C |
18: 10,070,260 (GRCm39) |
D1271G |
probably damaging |
Het |
Rprd1a |
T |
G |
18: 24,641,280 (GRCm39) |
E112A |
probably benign |
Het |
Sacm1l |
A |
T |
9: 123,411,384 (GRCm39) |
D391V |
probably damaging |
Het |
Serpina3f |
A |
T |
12: 104,185,737 (GRCm39) |
H314L |
probably benign |
Het |
Setd5 |
T |
A |
6: 113,127,853 (GRCm39) |
S1269T |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,308,335 (GRCm39) |
E740G |
probably damaging |
Het |
Tcaf1 |
T |
A |
6: 42,663,742 (GRCm39) |
Q46L |
probably damaging |
Het |
Tcam1 |
G |
A |
11: 106,173,618 (GRCm39) |
A21T |
probably benign |
Het |
Tchh |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
3: 93,354,015 (GRCm39) |
|
probably benign |
Het |
Ttll11 |
A |
T |
2: 35,792,985 (GRCm39) |
L286H |
probably damaging |
Het |
Usp1 |
A |
G |
4: 98,822,848 (GRCm39) |
T721A |
probably benign |
Het |
Vps41 |
T |
C |
13: 18,998,403 (GRCm39) |
S241P |
possibly damaging |
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 |
|
R2096:Phip
|
UTSW |
9 |
82,797,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
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 |
|