Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
G |
A |
8: 120,886,723 (GRCm39) |
E342K |
possibly damaging |
Het |
9430015G10Rik |
T |
G |
4: 156,203,649 (GRCm39) |
V34G |
probably damaging |
Het |
Alkbh3 |
T |
C |
2: 93,838,437 (GRCm39) |
S44G |
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,439,555 (GRCm39) |
C613S |
probably benign |
Het |
Aplp2 |
G |
A |
9: 31,072,645 (GRCm39) |
R488C |
probably damaging |
Het |
Arid1b |
A |
G |
17: 5,387,095 (GRCm39) |
N1463S |
probably benign |
Het |
Atxn2l |
A |
T |
7: 126,100,441 (GRCm39) |
L125Q |
probably damaging |
Het |
Cd3d |
A |
G |
9: 44,897,634 (GRCm39) |
K172E |
probably benign |
Het |
Chd7 |
T |
A |
4: 8,805,234 (GRCm39) |
D764E |
probably benign |
Het |
Col19a1 |
T |
C |
1: 24,569,089 (GRCm39) |
I220V |
unknown |
Het |
Cpq |
T |
C |
15: 33,497,493 (GRCm39) |
I411T |
probably benign |
Het |
Crybg2 |
C |
A |
4: 133,792,844 (GRCm39) |
H160N |
probably benign |
Het |
Cryl1 |
A |
T |
14: 57,513,013 (GRCm39) |
C285S |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,909,365 (GRCm39) |
D1326G |
probably damaging |
Het |
Dgkh |
A |
G |
14: 78,962,459 (GRCm39) |
V24A |
probably benign |
Het |
Dnajb4 |
A |
C |
3: 151,892,154 (GRCm39) |
S226R |
probably benign |
Het |
Dnm3 |
A |
T |
1: 161,819,622 (GRCm39) |
I850N |
possibly damaging |
Het |
Dtna |
G |
T |
18: 23,758,253 (GRCm39) |
|
probably null |
Het |
Efcab6 |
G |
T |
15: 83,834,125 (GRCm39) |
D494E |
probably benign |
Het |
Fam169a |
G |
T |
13: 97,263,196 (GRCm39) |
E550* |
probably null |
Het |
Fbxw7 |
A |
G |
3: 84,832,988 (GRCm39) |
N10S |
probably benign |
Het |
Flrt2 |
T |
C |
12: 95,747,528 (GRCm39) |
F622S |
probably damaging |
Het |
Gprc5d |
G |
A |
6: 135,093,355 (GRCm39) |
T184I |
possibly damaging |
Het |
Grem2 |
A |
G |
1: 174,664,693 (GRCm39) |
V52A |
probably damaging |
Het |
Gtf3c2 |
G |
T |
5: 31,327,533 (GRCm39) |
T310N |
probably damaging |
Het |
H2-T13 |
T |
A |
17: 36,394,770 (GRCm39) |
N51I |
probably damaging |
Het |
Hyou1 |
A |
G |
9: 44,295,759 (GRCm39) |
D338G |
possibly damaging |
Het |
Ifna6 |
T |
C |
4: 88,745,971 (GRCm39) |
S107P |
probably benign |
Het |
Kif14 |
G |
T |
1: 136,399,191 (GRCm39) |
G451C |
probably benign |
Het |
Kit |
T |
A |
5: 75,798,019 (GRCm39) |
F436I |
probably damaging |
Het |
Lonp2 |
G |
A |
8: 87,440,636 (GRCm39) |
C751Y |
probably damaging |
Het |
Lonrf1 |
C |
A |
8: 36,716,375 (GRCm39) |
G87C |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,309,687 (GRCm39) |
|
probably null |
Het |
Lrrc37 |
G |
T |
11: 103,505,738 (GRCm39) |
Q2077K |
probably benign |
Het |
Mkln1 |
A |
G |
6: 31,469,584 (GRCm39) |
H598R |
probably damaging |
Het |
Mmaa |
T |
C |
8: 79,994,774 (GRCm39) |
H344R |
probably benign |
Het |
Myh7 |
C |
G |
14: 55,226,258 (GRCm39) |
D461H |
probably damaging |
Het |
Myh7b |
T |
G |
2: 155,462,323 (GRCm39) |
L342R |
probably damaging |
Het |
Or12e8 |
A |
G |
2: 87,187,871 (GRCm39) |
N28D |
probably benign |
Het |
Or2h2b-ps1 |
C |
T |
17: 37,480,847 (GRCm39) |
G129R |
probably damaging |
Het |
Or4f4-ps1 |
T |
A |
2: 111,330,497 (GRCm39) |
I300K |
probably damaging |
Het |
Or7e178 |
A |
T |
9: 20,225,319 (GRCm39) |
V299E |
possibly damaging |
Het |
Pfn4 |
C |
T |
12: 4,824,414 (GRCm39) |
T47I |
possibly damaging |
Het |
Pklr |
T |
C |
3: 89,048,649 (GRCm39) |
L104P |
probably damaging |
Het |
Plcxd2 |
A |
G |
16: 45,800,693 (GRCm39) |
V177A |
probably benign |
Het |
Pramel16 |
T |
C |
4: 143,675,822 (GRCm39) |
S335G |
probably benign |
Het |
Prdm10 |
G |
T |
9: 31,268,528 (GRCm39) |
A826S |
probably damaging |
Het |
Prrt4 |
A |
G |
6: 29,177,455 (GRCm39) |
S105P |
probably benign |
Het |
Prss51 |
T |
A |
14: 64,334,937 (GRCm39) |
V164E |
probably damaging |
Het |
Psap |
T |
C |
10: 60,135,634 (GRCm39) |
V360A |
probably damaging |
Het |
Psg22 |
T |
C |
7: 18,452,267 (GRCm39) |
|
probably null |
Het |
Qrfprl |
A |
G |
6: 65,418,357 (GRCm39) |
H23R |
|
Het |
Rad51 |
A |
G |
2: 118,962,071 (GRCm39) |
Q206R |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,664,874 (GRCm39) |
K277R |
probably benign |
Het |
Rassf2 |
T |
A |
2: 131,847,297 (GRCm39) |
T103S |
probably benign |
Het |
Rbm15b |
T |
A |
9: 106,763,142 (GRCm39) |
H342L |
possibly damaging |
Het |
Rsf1 |
G |
GACCGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Scaf8 |
T |
C |
17: 3,237,909 (GRCm39) |
F561L |
probably damaging |
Het |
Scn1a |
G |
A |
2: 66,134,004 (GRCm39) |
A130V |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,531,221 (GRCm39) |
E552G |
probably damaging |
Het |
Slc39a14 |
T |
A |
14: 70,551,124 (GRCm39) |
R183W |
probably damaging |
Het |
Slfn1 |
A |
T |
11: 83,012,089 (GRCm39) |
K68N |
possibly damaging |
Het |
Slx4ip |
A |
G |
2: 136,909,914 (GRCm39) |
D303G |
probably damaging |
Het |
Snx17 |
T |
A |
5: 31,352,804 (GRCm39) |
F101Y |
probably damaging |
Het |
Spata31e3 |
T |
G |
13: 50,401,131 (GRCm39) |
R398S |
probably benign |
Het |
Specc1l |
C |
A |
10: 75,066,642 (GRCm39) |
N30K |
probably benign |
Het |
Spmip2 |
A |
G |
3: 79,313,167 (GRCm39) |
I80M |
probably damaging |
Het |
Tbx19 |
A |
G |
1: 164,966,768 (GRCm39) |
S369P |
probably benign |
Het |
Usp17ld |
T |
C |
7: 102,899,489 (GRCm39) |
H481R |
probably damaging |
Het |
Wnt2 |
A |
G |
6: 17,990,036 (GRCm39) |
L287P |
probably benign |
Het |
Zfhx4 |
G |
T |
3: 5,462,016 (GRCm39) |
M1230I |
probably damaging |
Het |
Zfp1 |
T |
C |
8: 112,396,794 (GRCm39) |
C272R |
not run |
Het |
Zfp458 |
A |
G |
13: 67,407,664 (GRCm39) |
S64P |
possibly damaging |
Het |
|
Other mutations in Pcsk5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Pcsk5
|
APN |
19 |
17,488,785 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL00423:Pcsk5
|
APN |
19 |
17,619,923 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01315:Pcsk5
|
APN |
19 |
17,429,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01372:Pcsk5
|
APN |
19 |
17,595,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01738:Pcsk5
|
APN |
19 |
17,411,144 (GRCm39) |
splice site |
probably benign |
|
IGL01874:Pcsk5
|
APN |
19 |
17,573,041 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02070:Pcsk5
|
APN |
19 |
17,416,406 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02311:Pcsk5
|
APN |
19 |
17,410,784 (GRCm39) |
nonsense |
probably null |
|
IGL02436:Pcsk5
|
APN |
19 |
17,542,072 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02498:Pcsk5
|
APN |
19 |
17,488,920 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02504:Pcsk5
|
APN |
19 |
17,455,236 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02664:Pcsk5
|
APN |
19 |
17,434,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02735:Pcsk5
|
APN |
19 |
17,652,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02941:Pcsk5
|
APN |
19 |
17,424,865 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4377001:Pcsk5
|
UTSW |
19 |
17,416,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R0007:Pcsk5
|
UTSW |
19 |
17,632,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0007:Pcsk5
|
UTSW |
19 |
17,632,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:Pcsk5
|
UTSW |
19 |
17,542,179 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0032:Pcsk5
|
UTSW |
19 |
17,542,179 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0373:Pcsk5
|
UTSW |
19 |
17,632,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Pcsk5
|
UTSW |
19 |
17,692,133 (GRCm39) |
missense |
probably benign |
0.06 |
R0843:Pcsk5
|
UTSW |
19 |
17,632,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1014:Pcsk5
|
UTSW |
19 |
17,542,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R1221:Pcsk5
|
UTSW |
19 |
17,814,512 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1435:Pcsk5
|
UTSW |
19 |
17,541,246 (GRCm39) |
nonsense |
probably null |
|
R1471:Pcsk5
|
UTSW |
19 |
17,545,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Pcsk5
|
UTSW |
19 |
17,632,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Pcsk5
|
UTSW |
19 |
17,413,964 (GRCm39) |
missense |
probably benign |
0.00 |
R1614:Pcsk5
|
UTSW |
19 |
17,492,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Pcsk5
|
UTSW |
19 |
17,424,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R1671:Pcsk5
|
UTSW |
19 |
17,432,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Pcsk5
|
UTSW |
19 |
17,729,458 (GRCm39) |
missense |
probably benign |
0.15 |
R1793:Pcsk5
|
UTSW |
19 |
17,432,114 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1855:Pcsk5
|
UTSW |
19 |
17,492,556 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1909:Pcsk5
|
UTSW |
19 |
17,410,825 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Pcsk5
|
UTSW |
19 |
17,410,782 (GRCm39) |
missense |
unknown |
|
R2006:Pcsk5
|
UTSW |
19 |
17,455,280 (GRCm39) |
missense |
probably benign |
0.32 |
R2045:Pcsk5
|
UTSW |
19 |
17,558,508 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2061:Pcsk5
|
UTSW |
19 |
17,432,236 (GRCm39) |
missense |
probably benign |
0.03 |
R2110:Pcsk5
|
UTSW |
19 |
17,450,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2402:Pcsk5
|
UTSW |
19 |
17,452,198 (GRCm39) |
nonsense |
probably null |
|
R2496:Pcsk5
|
UTSW |
19 |
17,443,522 (GRCm39) |
nonsense |
probably null |
|
R4115:Pcsk5
|
UTSW |
19 |
17,410,783 (GRCm39) |
missense |
unknown |
|
R4504:Pcsk5
|
UTSW |
19 |
17,429,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R4616:Pcsk5
|
UTSW |
19 |
17,538,114 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Pcsk5
|
UTSW |
19 |
17,450,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Pcsk5
|
UTSW |
19 |
17,502,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R4761:Pcsk5
|
UTSW |
19 |
17,814,512 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4789:Pcsk5
|
UTSW |
19 |
17,410,963 (GRCm39) |
missense |
probably benign |
0.09 |
R4880:Pcsk5
|
UTSW |
19 |
17,425,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Pcsk5
|
UTSW |
19 |
17,492,499 (GRCm39) |
critical splice donor site |
probably null |
|
R5114:Pcsk5
|
UTSW |
19 |
17,652,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Pcsk5
|
UTSW |
19 |
17,440,798 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5193:Pcsk5
|
UTSW |
19 |
17,542,174 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5279:Pcsk5
|
UTSW |
19 |
17,573,022 (GRCm39) |
splice site |
probably null |
|
R5334:Pcsk5
|
UTSW |
19 |
17,439,215 (GRCm39) |
missense |
probably benign |
0.00 |
R5369:Pcsk5
|
UTSW |
19 |
17,558,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R5451:Pcsk5
|
UTSW |
19 |
17,440,720 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5547:Pcsk5
|
UTSW |
19 |
17,729,488 (GRCm39) |
missense |
probably benign |
0.08 |
R5630:Pcsk5
|
UTSW |
19 |
17,553,195 (GRCm39) |
missense |
probably benign |
0.04 |
R5805:Pcsk5
|
UTSW |
19 |
17,434,193 (GRCm39) |
missense |
probably benign |
0.01 |
R6063:Pcsk5
|
UTSW |
19 |
17,432,045 (GRCm39) |
critical splice donor site |
probably null |
|
R6130:Pcsk5
|
UTSW |
19 |
17,488,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R6153:Pcsk5
|
UTSW |
19 |
17,488,856 (GRCm39) |
missense |
probably damaging |
0.98 |
R6163:Pcsk5
|
UTSW |
19 |
17,450,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Pcsk5
|
UTSW |
19 |
17,814,317 (GRCm39) |
critical splice donor site |
probably null |
|
R6228:Pcsk5
|
UTSW |
19 |
17,558,631 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6426:Pcsk5
|
UTSW |
19 |
17,595,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Pcsk5
|
UTSW |
19 |
17,488,744 (GRCm39) |
missense |
probably benign |
0.00 |
R6648:Pcsk5
|
UTSW |
19 |
17,553,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R6789:Pcsk5
|
UTSW |
19 |
17,434,150 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6807:Pcsk5
|
UTSW |
19 |
17,549,986 (GRCm39) |
splice site |
probably null |
|
R6837:Pcsk5
|
UTSW |
19 |
17,416,448 (GRCm39) |
missense |
probably benign |
0.01 |
R6998:Pcsk5
|
UTSW |
19 |
17,450,476 (GRCm39) |
missense |
probably benign |
0.20 |
R7051:Pcsk5
|
UTSW |
19 |
17,411,095 (GRCm39) |
missense |
probably benign |
0.00 |
R7164:Pcsk5
|
UTSW |
19 |
17,429,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R7173:Pcsk5
|
UTSW |
19 |
17,455,241 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7348:Pcsk5
|
UTSW |
19 |
17,434,182 (GRCm39) |
nonsense |
probably null |
|
R7360:Pcsk5
|
UTSW |
19 |
17,492,577 (GRCm39) |
missense |
probably benign |
0.00 |
R7407:Pcsk5
|
UTSW |
19 |
17,652,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Pcsk5
|
UTSW |
19 |
17,487,600 (GRCm39) |
missense |
probably benign |
0.31 |
R7521:Pcsk5
|
UTSW |
19 |
17,432,196 (GRCm39) |
missense |
probably benign |
0.29 |
R7525:Pcsk5
|
UTSW |
19 |
17,619,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Pcsk5
|
UTSW |
19 |
17,814,336 (GRCm39) |
missense |
probably benign |
0.01 |
R7566:Pcsk5
|
UTSW |
19 |
17,549,821 (GRCm39) |
missense |
probably benign |
|
R7631:Pcsk5
|
UTSW |
19 |
17,542,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Pcsk5
|
UTSW |
19 |
17,434,168 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7677:Pcsk5
|
UTSW |
19 |
17,558,593 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7903:Pcsk5
|
UTSW |
19 |
17,549,847 (GRCm39) |
missense |
probably damaging |
0.98 |
R7938:Pcsk5
|
UTSW |
19 |
17,443,549 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8025:Pcsk5
|
UTSW |
19 |
17,538,415 (GRCm39) |
intron |
probably benign |
|
R8032:Pcsk5
|
UTSW |
19 |
17,692,151 (GRCm39) |
missense |
probably damaging |
0.98 |
R8064:Pcsk5
|
UTSW |
19 |
17,692,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Pcsk5
|
UTSW |
19 |
17,487,530 (GRCm39) |
critical splice donor site |
probably null |
|
R8193:Pcsk5
|
UTSW |
19 |
17,563,415 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8408:Pcsk5
|
UTSW |
19 |
17,410,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8466:Pcsk5
|
UTSW |
19 |
17,549,864 (GRCm39) |
nonsense |
probably null |
|
R8739:Pcsk5
|
UTSW |
19 |
17,432,138 (GRCm39) |
missense |
probably benign |
0.00 |
R8753:Pcsk5
|
UTSW |
19 |
17,446,408 (GRCm39) |
missense |
probably benign |
0.00 |
R8797:Pcsk5
|
UTSW |
19 |
17,443,472 (GRCm39) |
missense |
probably benign |
0.00 |
R8944:Pcsk5
|
UTSW |
19 |
17,452,275 (GRCm39) |
missense |
probably damaging |
0.96 |
R9041:Pcsk5
|
UTSW |
19 |
17,538,132 (GRCm39) |
nonsense |
probably null |
|
R9135:Pcsk5
|
UTSW |
19 |
17,563,472 (GRCm39) |
missense |
|
|
R9288:Pcsk5
|
UTSW |
19 |
17,814,345 (GRCm39) |
missense |
probably benign |
0.10 |
R9406:Pcsk5
|
UTSW |
19 |
17,771,097 (GRCm39) |
missense |
probably benign |
0.14 |
R9581:Pcsk5
|
UTSW |
19 |
17,432,196 (GRCm39) |
missense |
probably benign |
|
R9592:Pcsk5
|
UTSW |
19 |
17,652,899 (GRCm39) |
nonsense |
probably null |
|
R9659:Pcsk5
|
UTSW |
19 |
17,455,245 (GRCm39) |
missense |
probably benign |
0.00 |
R9788:Pcsk5
|
UTSW |
19 |
17,455,245 (GRCm39) |
missense |
probably benign |
0.00 |
X0023:Pcsk5
|
UTSW |
19 |
17,452,236 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0063:Pcsk5
|
UTSW |
19 |
17,424,968 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Pcsk5
|
UTSW |
19 |
17,440,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|