Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd8 |
A |
T |
8: 71,914,165 (GRCm39) |
C154* |
probably null |
Het |
Ada |
A |
G |
2: 163,570,108 (GRCm39) |
|
probably null |
Het |
Birc6 |
G |
A |
17: 74,886,276 (GRCm39) |
V535I |
probably damaging |
Het |
Bptf |
T |
C |
11: 106,968,509 (GRCm39) |
N1058S |
probably null |
Het |
Cdadc1 |
C |
T |
14: 59,823,898 (GRCm39) |
C198Y |
probably benign |
Het |
Chrna7 |
G |
A |
7: 62,755,863 (GRCm39) |
R228C |
probably damaging |
Het |
Cts6 |
T |
C |
13: 61,344,149 (GRCm39) |
N301S |
probably damaging |
Het |
Cts8 |
T |
A |
13: 61,398,756 (GRCm39) |
D250V |
probably damaging |
Het |
Cyp26a1 |
G |
T |
19: 37,687,518 (GRCm39) |
R235L |
possibly damaging |
Het |
Disc1 |
A |
T |
8: 125,944,844 (GRCm39) |
M598L |
probably benign |
Het |
Ear6 |
T |
A |
14: 52,091,681 (GRCm39) |
V76D |
possibly damaging |
Het |
Grifin |
A |
G |
5: 140,549,036 (GRCm39) |
*145R |
probably null |
Het |
Htr2b |
T |
G |
1: 86,038,363 (GRCm39) |
E11A |
probably damaging |
Het |
Krtap4-9 |
T |
A |
11: 99,676,255 (GRCm39) |
|
probably benign |
Het |
Larp4b |
A |
C |
13: 9,218,829 (GRCm39) |
H522P |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,363,425 (GRCm39) |
|
probably null |
Het |
Mdfic |
T |
C |
6: 15,770,516 (GRCm39) |
L174P |
possibly damaging |
Het |
Mmp17 |
A |
G |
5: 129,683,469 (GRCm39) |
E535G |
probably benign |
Het |
Nfxl1 |
A |
T |
5: 72,685,852 (GRCm39) |
|
probably null |
Het |
Nynrin |
A |
T |
14: 56,100,989 (GRCm39) |
T260S |
probably benign |
Het |
Or4k44 |
C |
T |
2: 111,368,124 (GRCm39) |
G170D |
probably damaging |
Het |
Or7e168 |
A |
T |
9: 19,720,271 (GRCm39) |
Y219F |
possibly damaging |
Het |
Or8b1c |
A |
T |
9: 38,384,585 (GRCm39) |
I181F |
possibly damaging |
Het |
Pbx1 |
G |
T |
1: 168,037,103 (GRCm39) |
D109E |
probably damaging |
Het |
Pde4d |
A |
T |
13: 109,253,476 (GRCm39) |
H101L |
probably benign |
Het |
Pdlim3 |
T |
C |
8: 46,361,639 (GRCm39) |
I155T |
possibly damaging |
Het |
Plekha5 |
T |
A |
6: 140,471,655 (GRCm39) |
Y26* |
probably null |
Het |
Prpf6 |
T |
A |
2: 181,263,713 (GRCm39) |
L191* |
probably null |
Het |
Rabl6 |
A |
G |
2: 25,492,459 (GRCm39) |
V80A |
possibly damaging |
Het |
Rp1 |
T |
C |
1: 4,381,503 (GRCm39) |
|
probably benign |
Het |
Sec14l1 |
A |
G |
11: 117,047,676 (GRCm39) |
S698G |
probably damaging |
Het |
Skic2 |
A |
G |
17: 35,063,412 (GRCm39) |
S622P |
possibly damaging |
Het |
Slc19a1 |
G |
A |
10: 76,885,440 (GRCm39) |
G447S |
probably benign |
Het |
Slc2a6 |
A |
T |
2: 26,913,143 (GRCm39) |
Y383* |
probably null |
Het |
Slc9a9 |
C |
A |
9: 94,818,424 (GRCm39) |
Q273K |
probably benign |
Het |
Spint2 |
A |
G |
7: 28,963,131 (GRCm39) |
Y56H |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,472,146 (GRCm39) |
M123K |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,074,621 (GRCm39) |
|
probably null |
Het |
Trdn |
A |
C |
10: 33,342,450 (GRCm39) |
K619N |
probably benign |
Het |
Ttll13 |
A |
G |
7: 79,899,924 (GRCm39) |
T119A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,615,990 (GRCm39) |
Y8324C |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,602 (GRCm39) |
|
probably benign |
Het |
Vav2 |
A |
G |
2: 27,186,231 (GRCm39) |
L208P |
probably damaging |
Het |
Vmn1r179 |
A |
G |
7: 23,628,342 (GRCm39) |
I178V |
probably benign |
Het |
Vmn1r210 |
T |
C |
13: 23,011,705 (GRCm39) |
M194V |
possibly damaging |
Het |
Vmn2r103 |
A |
T |
17: 20,032,166 (GRCm39) |
T647S |
probably benign |
Het |
Wdr49 |
T |
A |
3: 75,246,765 (GRCm39) |
H289L |
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,590,978 (GRCm39) |
|
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 |
R3962:Wnk2
|
UTSW |
13 |
49,224,453 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|
|