Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
T |
C |
11: 48,838,803 (GRCm39) |
T595A |
possibly damaging |
Het |
Abca12 |
A |
T |
1: 71,313,674 (GRCm39) |
|
probably null |
Het |
Ablim2 |
C |
T |
5: 35,969,519 (GRCm39) |
R211C |
probably damaging |
Het |
Actn4 |
C |
A |
7: 28,597,647 (GRCm39) |
|
probably null |
Het |
B3gnt5 |
A |
G |
16: 19,587,798 (GRCm39) |
S6G |
probably benign |
Het |
Bod1l |
T |
G |
5: 41,966,064 (GRCm39) |
E2667A |
probably benign |
Het |
Ccdc13 |
G |
A |
9: 121,628,005 (GRCm39) |
|
probably benign |
Het |
Ccdc15 |
G |
T |
9: 37,231,782 (GRCm39) |
R181S |
probably damaging |
Het |
Ccnd1 |
G |
A |
7: 144,487,787 (GRCm39) |
T230M |
probably damaging |
Het |
Cdcp1 |
T |
C |
9: 123,011,446 (GRCm39) |
T344A |
possibly damaging |
Het |
Fam161a |
T |
C |
11: 22,973,507 (GRCm39) |
M275T |
possibly damaging |
Het |
Fbxo15 |
A |
G |
18: 84,977,372 (GRCm39) |
T95A |
probably benign |
Het |
Fndc5 |
T |
C |
4: 129,033,688 (GRCm39) |
V152A |
probably benign |
Het |
Galk2 |
A |
T |
2: 125,735,293 (GRCm39) |
N107I |
probably benign |
Het |
Glmn |
A |
T |
5: 107,708,911 (GRCm39) |
|
probably benign |
Het |
Gm5082 |
T |
C |
13: 41,809,894 (GRCm39) |
|
noncoding transcript |
Het |
Gm5828 |
C |
T |
1: 16,838,868 (GRCm39) |
|
noncoding transcript |
Het |
Haus6 |
C |
T |
4: 86,530,041 (GRCm39) |
A4T |
possibly damaging |
Het |
Hmgcs2 |
G |
A |
3: 98,198,354 (GRCm39) |
V86M |
possibly damaging |
Het |
Hrg |
G |
A |
16: 22,774,825 (GRCm39) |
V152I |
possibly damaging |
Het |
Itga2 |
A |
T |
13: 114,976,054 (GRCm39) |
V1106E |
probably damaging |
Het |
Itga9 |
G |
A |
9: 118,457,254 (GRCm39) |
D122N |
possibly damaging |
Het |
Kif21a |
T |
A |
15: 90,869,612 (GRCm39) |
E413V |
probably damaging |
Het |
Klk1 |
A |
G |
7: 43,878,973 (GRCm39) |
T256A |
possibly damaging |
Het |
L1td1 |
T |
C |
4: 98,625,686 (GRCm39) |
V627A |
probably benign |
Het |
Larp4 |
C |
A |
15: 99,910,026 (GRCm39) |
Q652K |
probably damaging |
Het |
Ltbp3 |
G |
A |
19: 5,804,050 (GRCm39) |
R854Q |
probably benign |
Het |
Minar1 |
G |
A |
9: 89,483,963 (GRCm39) |
T478I |
probably damaging |
Het |
Moxd2 |
T |
A |
6: 40,862,331 (GRCm39) |
M163L |
probably benign |
Het |
Myo15a |
G |
A |
11: 60,370,654 (GRCm39) |
R1138H |
probably benign |
Het |
Oasl2 |
A |
G |
5: 115,035,808 (GRCm39) |
D28G |
probably benign |
Het |
Or6c207 |
A |
T |
10: 129,104,535 (GRCm39) |
I219N |
probably damaging |
Het |
Platr26 |
A |
T |
2: 71,549,849 (GRCm39) |
|
noncoding transcript |
Het |
Ptdss1 |
A |
G |
13: 67,142,075 (GRCm39) |
H411R |
probably benign |
Het |
Ptpra |
A |
G |
2: 30,325,672 (GRCm39) |
T147A |
probably damaging |
Het |
Rfx2 |
T |
C |
17: 57,092,302 (GRCm39) |
Y307C |
probably damaging |
Het |
Rtn3 |
T |
C |
19: 7,435,510 (GRCm39) |
S142G |
probably damaging |
Het |
Shisa6 |
A |
G |
11: 66,108,302 (GRCm39) |
V525A |
probably damaging |
Het |
Slc4a3 |
A |
G |
1: 75,533,398 (GRCm39) |
S1007G |
probably damaging |
Het |
Spmip5 |
A |
G |
19: 58,777,541 (GRCm39) |
Y82H |
probably damaging |
Het |
Srsf3 |
C |
T |
17: 29,255,430 (GRCm39) |
|
probably benign |
Het |
Taar8a |
A |
G |
10: 23,953,054 (GRCm39) |
I219M |
probably damaging |
Het |
Tars2 |
A |
G |
3: 95,662,068 (GRCm39) |
|
probably null |
Het |
Tfap2d |
A |
G |
1: 19,189,189 (GRCm39) |
N245S |
probably damaging |
Het |
Tlr6 |
T |
A |
5: 65,112,328 (GRCm39) |
H193L |
probably benign |
Het |
Tomm20l |
T |
C |
12: 71,164,352 (GRCm39) |
V78A |
probably benign |
Het |
Tsc2 |
G |
A |
17: 24,840,140 (GRCm39) |
|
probably benign |
Het |
Usp2 |
A |
G |
9: 43,986,954 (GRCm39) |
D84G |
possibly damaging |
Het |
V1ra8 |
A |
G |
6: 90,180,466 (GRCm39) |
N223S |
probably benign |
Het |
|
Other mutations in Wnk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01518:Wnk2
|
APN |
13 |
49,221,668 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01575:Wnk2
|
APN |
13 |
49,300,152 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01601:Wnk2
|
APN |
13 |
49,230,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01775:Wnk2
|
APN |
13 |
49,224,586 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02013:Wnk2
|
APN |
13 |
49,235,510 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02016:Wnk2
|
APN |
13 |
49,210,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02167:Wnk2
|
APN |
13 |
49,224,601 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02174:Wnk2
|
APN |
13 |
49,210,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02210:Wnk2
|
APN |
13 |
49,244,345 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02228:Wnk2
|
APN |
13 |
49,210,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02282:Wnk2
|
APN |
13 |
49,221,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02319:Wnk2
|
APN |
13 |
49,214,914 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02394:Wnk2
|
APN |
13 |
49,235,375 (GRCm39) |
splice site |
probably null |
|
IGL02624:Wnk2
|
APN |
13 |
49,256,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02743:Wnk2
|
APN |
13 |
49,248,920 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03012:Wnk2
|
APN |
13 |
49,197,865 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03166:Wnk2
|
APN |
13 |
49,224,520 (GRCm39) |
nonsense |
probably null |
|
R0034:Wnk2
|
UTSW |
13 |
49,221,556 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0385:Wnk2
|
UTSW |
13 |
49,221,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R0423:Wnk2
|
UTSW |
13 |
49,248,894 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0504:Wnk2
|
UTSW |
13 |
49,238,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Wnk2
|
UTSW |
13 |
49,238,870 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0653:Wnk2
|
UTSW |
13 |
49,210,492 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1135:Wnk2
|
UTSW |
13 |
49,230,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Wnk2
|
UTSW |
13 |
49,224,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Wnk2
|
UTSW |
13 |
49,235,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Wnk2
|
UTSW |
13 |
49,235,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Wnk2
|
UTSW |
13 |
49,235,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Wnk2
|
UTSW |
13 |
49,235,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R1480:Wnk2
|
UTSW |
13 |
49,210,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Wnk2
|
UTSW |
13 |
49,214,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:Wnk2
|
UTSW |
13 |
49,214,202 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1891:Wnk2
|
UTSW |
13 |
49,206,200 (GRCm39) |
nonsense |
probably null |
|
R1966:Wnk2
|
UTSW |
13 |
49,192,487 (GRCm39) |
missense |
probably damaging |
0.96 |
R2001:Wnk2
|
UTSW |
13 |
49,232,158 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2310:Wnk2
|
UTSW |
13 |
49,204,053 (GRCm39) |
missense |
probably damaging |
0.97 |
R2356:Wnk2
|
UTSW |
13 |
49,192,644 (GRCm39) |
nonsense |
probably null |
|
R2406:Wnk2
|
UTSW |
13 |
49,214,964 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2519:Wnk2
|
UTSW |
13 |
49,224,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R4160:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4226:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4227:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Wnk2
|
UTSW |
13 |
49,214,604 (GRCm39) |
missense |
probably benign |
0.33 |
R4304:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Wnk2
|
UTSW |
13 |
49,244,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4655:Wnk2
|
UTSW |
13 |
49,210,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Wnk2
|
UTSW |
13 |
49,300,708 (GRCm39) |
start codon destroyed |
unknown |
|
R4887:Wnk2
|
UTSW |
13 |
49,224,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Wnk2
|
UTSW |
13 |
49,224,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4945:Wnk2
|
UTSW |
13 |
49,210,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Wnk2
|
UTSW |
13 |
49,214,637 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5243:Wnk2
|
UTSW |
13 |
49,226,054 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5370:Wnk2
|
UTSW |
13 |
49,256,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5771:Wnk2
|
UTSW |
13 |
49,256,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Wnk2
|
UTSW |
13 |
49,220,782 (GRCm39) |
missense |
probably damaging |
0.98 |
R5900:Wnk2
|
UTSW |
13 |
49,256,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Wnk2
|
UTSW |
13 |
49,229,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R5912:Wnk2
|
UTSW |
13 |
49,214,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:Wnk2
|
UTSW |
13 |
49,231,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R6028:Wnk2
|
UTSW |
13 |
49,229,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R6074:Wnk2
|
UTSW |
13 |
49,204,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R6171:Wnk2
|
UTSW |
13 |
49,214,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6368:Wnk2
|
UTSW |
13 |
49,214,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R6467:Wnk2
|
UTSW |
13 |
49,300,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6501:Wnk2
|
UTSW |
13 |
49,300,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Wnk2
|
UTSW |
13 |
49,220,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Wnk2
|
UTSW |
13 |
49,224,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Wnk2
|
UTSW |
13 |
49,254,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7011:Wnk2
|
UTSW |
13 |
49,224,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R7097:Wnk2
|
UTSW |
13 |
49,256,314 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7121:Wnk2
|
UTSW |
13 |
49,300,653 (GRCm39) |
missense |
probably benign |
0.26 |
R7123:Wnk2
|
UTSW |
13 |
49,235,462 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7423:Wnk2
|
UTSW |
13 |
49,191,608 (GRCm39) |
missense |
probably benign |
0.07 |
R7502:Wnk2
|
UTSW |
13 |
49,300,720 (GRCm39) |
splice site |
probably null |
|
R7529:Wnk2
|
UTSW |
13 |
49,254,457 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7751:Wnk2
|
UTSW |
13 |
49,231,493 (GRCm39) |
missense |
unknown |
|
R7979:Wnk2
|
UTSW |
13 |
49,248,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Wnk2
|
UTSW |
13 |
49,244,459 (GRCm39) |
missense |
probably damaging |
0.99 |
R8121:Wnk2
|
UTSW |
13 |
49,214,415 (GRCm39) |
nonsense |
probably null |
|
R8155:Wnk2
|
UTSW |
13 |
49,192,577 (GRCm39) |
missense |
unknown |
|
R8329:Wnk2
|
UTSW |
13 |
49,248,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Wnk2
|
UTSW |
13 |
49,203,958 (GRCm39) |
critical splice donor site |
probably null |
|
R8872:Wnk2
|
UTSW |
13 |
49,210,960 (GRCm39) |
missense |
probably benign |
0.00 |
R8919:Wnk2
|
UTSW |
13 |
49,221,711 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9091:Wnk2
|
UTSW |
13 |
49,224,505 (GRCm39) |
missense |
probably benign |
0.41 |
R9234:Wnk2
|
UTSW |
13 |
49,224,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R9262:Wnk2
|
UTSW |
13 |
49,221,430 (GRCm39) |
missense |
probably benign |
0.12 |
R9268:Wnk2
|
UTSW |
13 |
49,235,507 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9270:Wnk2
|
UTSW |
13 |
49,224,505 (GRCm39) |
missense |
probably benign |
0.41 |
R9386:Wnk2
|
UTSW |
13 |
49,220,822 (GRCm39) |
missense |
probably damaging |
0.98 |
R9582:Wnk2
|
UTSW |
13 |
49,210,975 (GRCm39) |
missense |
probably benign |
0.01 |
R9617:Wnk2
|
UTSW |
13 |
49,192,453 (GRCm39) |
missense |
unknown |
|
R9625:Wnk2
|
UTSW |
13 |
49,254,445 (GRCm39) |
missense |
probably benign |
0.20 |
R9794:Wnk2
|
UTSW |
13 |
49,229,674 (GRCm39) |
missense |
probably benign |
0.02 |
RF023:Wnk2
|
UTSW |
13 |
49,300,255 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Wnk2
|
UTSW |
13 |
49,214,418 (GRCm39) |
missense |
probably damaging |
0.99 |
X0063:Wnk2
|
UTSW |
13 |
49,192,453 (GRCm39) |
missense |
unknown |
|
Z1176:Wnk2
|
UTSW |
13 |
49,191,537 (GRCm39) |
missense |
unknown |
|
|