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 |
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 |
Pcsk5 |
T |
A |
19: 17,416,444 (GRCm39) |
Y1668F |
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 Alpk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Alpk2
|
APN |
18 |
65,438,894 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00478:Alpk2
|
APN |
18 |
65,440,297 (GRCm39) |
nonsense |
probably null |
|
IGL00898:Alpk2
|
APN |
18 |
65,483,644 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00978:Alpk2
|
APN |
18 |
65,424,605 (GRCm39) |
splice site |
probably benign |
|
IGL01093:Alpk2
|
APN |
18 |
65,482,400 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01094:Alpk2
|
APN |
18 |
65,439,673 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01109:Alpk2
|
APN |
18 |
65,440,211 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01370:Alpk2
|
APN |
18 |
65,483,662 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01393:Alpk2
|
APN |
18 |
65,440,779 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01629:Alpk2
|
APN |
18 |
65,433,113 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Alpk2
|
APN |
18 |
65,437,824 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01983:Alpk2
|
APN |
18 |
65,483,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02294:Alpk2
|
APN |
18 |
65,439,146 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL02333:Alpk2
|
APN |
18 |
65,482,551 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02493:Alpk2
|
APN |
18 |
65,483,402 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02551:Alpk2
|
APN |
18 |
65,505,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02864:Alpk2
|
APN |
18 |
65,440,670 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02901:Alpk2
|
APN |
18 |
65,439,482 (GRCm39) |
missense |
probably benign |
|
IGL02954:Alpk2
|
APN |
18 |
65,439,207 (GRCm39) |
missense |
probably benign |
|
IGL03257:Alpk2
|
APN |
18 |
65,482,945 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03389:Alpk2
|
APN |
18 |
65,437,937 (GRCm39) |
missense |
possibly damaging |
0.92 |
3-1:Alpk2
|
UTSW |
18 |
65,437,959 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4131001:Alpk2
|
UTSW |
18 |
65,439,450 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0098:Alpk2
|
UTSW |
18 |
65,482,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Alpk2
|
UTSW |
18 |
65,482,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Alpk2
|
UTSW |
18 |
65,439,230 (GRCm39) |
missense |
probably benign |
0.04 |
R0546:Alpk2
|
UTSW |
18 |
65,439,788 (GRCm39) |
missense |
probably benign |
0.05 |
R0628:Alpk2
|
UTSW |
18 |
65,440,367 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0658:Alpk2
|
UTSW |
18 |
65,482,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Alpk2
|
UTSW |
18 |
65,438,461 (GRCm39) |
missense |
probably damaging |
0.98 |
R0919:Alpk2
|
UTSW |
18 |
65,440,544 (GRCm39) |
missense |
probably benign |
|
R1069:Alpk2
|
UTSW |
18 |
65,438,085 (GRCm39) |
missense |
probably benign |
0.25 |
R1186:Alpk2
|
UTSW |
18 |
65,427,412 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1508:Alpk2
|
UTSW |
18 |
65,482,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Alpk2
|
UTSW |
18 |
65,483,275 (GRCm39) |
missense |
probably benign |
|
R1558:Alpk2
|
UTSW |
18 |
65,483,301 (GRCm39) |
missense |
probably benign |
|
R1600:Alpk2
|
UTSW |
18 |
65,511,108 (GRCm39) |
missense |
probably damaging |
0.96 |
R1664:Alpk2
|
UTSW |
18 |
65,482,944 (GRCm39) |
missense |
probably damaging |
0.96 |
R1672:Alpk2
|
UTSW |
18 |
65,414,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Alpk2
|
UTSW |
18 |
65,427,165 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2110:Alpk2
|
UTSW |
18 |
65,440,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2111:Alpk2
|
UTSW |
18 |
65,482,845 (GRCm39) |
missense |
probably benign |
|
R2113:Alpk2
|
UTSW |
18 |
65,438,754 (GRCm39) |
missense |
probably benign |
0.31 |
R2126:Alpk2
|
UTSW |
18 |
65,483,439 (GRCm39) |
nonsense |
probably null |
|
R2198:Alpk2
|
UTSW |
18 |
65,483,255 (GRCm39) |
missense |
probably benign |
0.42 |
R2227:Alpk2
|
UTSW |
18 |
65,511,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R2245:Alpk2
|
UTSW |
18 |
65,438,234 (GRCm39) |
missense |
probably benign |
0.02 |
R2282:Alpk2
|
UTSW |
18 |
65,440,697 (GRCm39) |
missense |
probably benign |
|
R2421:Alpk2
|
UTSW |
18 |
65,439,687 (GRCm39) |
missense |
probably benign |
0.00 |
R2512:Alpk2
|
UTSW |
18 |
65,483,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R3105:Alpk2
|
UTSW |
18 |
65,483,281 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3700:Alpk2
|
UTSW |
18 |
65,438,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R4205:Alpk2
|
UTSW |
18 |
65,438,282 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4239:Alpk2
|
UTSW |
18 |
65,433,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Alpk2
|
UTSW |
18 |
65,424,523 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4572:Alpk2
|
UTSW |
18 |
65,414,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Alpk2
|
UTSW |
18 |
65,440,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R4591:Alpk2
|
UTSW |
18 |
65,438,894 (GRCm39) |
missense |
probably benign |
0.27 |
R4595:Alpk2
|
UTSW |
18 |
65,422,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Alpk2
|
UTSW |
18 |
65,482,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R4815:Alpk2
|
UTSW |
18 |
65,483,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Alpk2
|
UTSW |
18 |
65,482,184 (GRCm39) |
missense |
probably benign |
|
R4910:Alpk2
|
UTSW |
18 |
65,399,357 (GRCm39) |
nonsense |
probably null |
|
R5042:Alpk2
|
UTSW |
18 |
65,483,579 (GRCm39) |
nonsense |
probably null |
|
R5295:Alpk2
|
UTSW |
18 |
65,438,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R5375:Alpk2
|
UTSW |
18 |
65,505,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5475:Alpk2
|
UTSW |
18 |
65,440,083 (GRCm39) |
missense |
probably benign |
0.16 |
R5480:Alpk2
|
UTSW |
18 |
65,482,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Alpk2
|
UTSW |
18 |
65,427,425 (GRCm39) |
splice site |
probably null |
|
R5503:Alpk2
|
UTSW |
18 |
65,439,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5595:Alpk2
|
UTSW |
18 |
65,399,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Alpk2
|
UTSW |
18 |
65,482,988 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Alpk2
|
UTSW |
18 |
65,438,532 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5862:Alpk2
|
UTSW |
18 |
65,440,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Alpk2
|
UTSW |
18 |
65,414,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Alpk2
|
UTSW |
18 |
65,440,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R5936:Alpk2
|
UTSW |
18 |
65,483,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R6142:Alpk2
|
UTSW |
18 |
65,438,456 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6291:Alpk2
|
UTSW |
18 |
65,438,972 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6339:Alpk2
|
UTSW |
18 |
65,482,877 (GRCm39) |
missense |
probably benign |
0.00 |
R6407:Alpk2
|
UTSW |
18 |
65,422,809 (GRCm39) |
missense |
probably benign |
0.22 |
R6487:Alpk2
|
UTSW |
18 |
65,399,254 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6667:Alpk2
|
UTSW |
18 |
65,440,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Alpk2
|
UTSW |
18 |
65,439,705 (GRCm39) |
missense |
probably benign |
|
R6833:Alpk2
|
UTSW |
18 |
65,439,480 (GRCm39) |
missense |
probably benign |
0.08 |
R6984:Alpk2
|
UTSW |
18 |
65,438,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6999:Alpk2
|
UTSW |
18 |
65,437,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R7157:Alpk2
|
UTSW |
18 |
65,399,348 (GRCm39) |
nonsense |
probably null |
|
R7167:Alpk2
|
UTSW |
18 |
65,440,049 (GRCm39) |
missense |
probably benign |
0.40 |
R7225:Alpk2
|
UTSW |
18 |
65,438,270 (GRCm39) |
missense |
probably benign |
0.00 |
R7409:Alpk2
|
UTSW |
18 |
65,440,023 (GRCm39) |
missense |
probably benign |
0.01 |
R7533:Alpk2
|
UTSW |
18 |
65,437,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Alpk2
|
UTSW |
18 |
65,439,887 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7589:Alpk2
|
UTSW |
18 |
65,433,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Alpk2
|
UTSW |
18 |
65,437,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:Alpk2
|
UTSW |
18 |
65,440,073 (GRCm39) |
missense |
probably benign |
0.03 |
R7722:Alpk2
|
UTSW |
18 |
65,483,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Alpk2
|
UTSW |
18 |
65,439,325 (GRCm39) |
nonsense |
probably null |
|
R7806:Alpk2
|
UTSW |
18 |
65,482,487 (GRCm39) |
missense |
probably benign |
|
R7953:Alpk2
|
UTSW |
18 |
65,482,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Alpk2
|
UTSW |
18 |
65,438,106 (GRCm39) |
missense |
probably benign |
0.01 |
R8043:Alpk2
|
UTSW |
18 |
65,482,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8063:Alpk2
|
UTSW |
18 |
65,483,417 (GRCm39) |
missense |
probably benign |
0.15 |
R8171:Alpk2
|
UTSW |
18 |
65,439,054 (GRCm39) |
missense |
probably benign |
0.00 |
R8280:Alpk2
|
UTSW |
18 |
65,440,274 (GRCm39) |
missense |
probably benign |
|
R8383:Alpk2
|
UTSW |
18 |
65,438,469 (GRCm39) |
missense |
probably benign |
0.03 |
R8414:Alpk2
|
UTSW |
18 |
65,440,542 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8791:Alpk2
|
UTSW |
18 |
65,438,597 (GRCm39) |
missense |
probably benign |
0.00 |
R8872:Alpk2
|
UTSW |
18 |
65,413,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Alpk2
|
UTSW |
18 |
65,439,783 (GRCm39) |
missense |
probably benign |
0.01 |
R9449:Alpk2
|
UTSW |
18 |
65,424,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Alpk2
|
UTSW |
18 |
65,399,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Alpk2
|
UTSW |
18 |
65,439,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Alpk2
|
UTSW |
18 |
65,482,646 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Alpk2
|
UTSW |
18 |
65,424,471 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Alpk2
|
UTSW |
18 |
65,440,542 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0063:Alpk2
|
UTSW |
18 |
65,440,434 (GRCm39) |
missense |
probably benign |
|
X0064:Alpk2
|
UTSW |
18 |
65,482,755 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Alpk2
|
UTSW |
18 |
65,438,682 (GRCm39) |
missense |
probably damaging |
0.98 |
|