Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110059E24Rik |
A |
G |
19: 21,608,129 (GRCm39) |
M1T |
probably null |
Het |
Abcg8 |
T |
C |
17: 85,000,172 (GRCm39) |
L243P |
probably damaging |
Het |
Ankrd27 |
A |
G |
7: 35,327,912 (GRCm39) |
T811A |
probably damaging |
Het |
Auts2 |
T |
C |
5: 131,503,919 (GRCm39) |
N188S |
probably null |
Het |
Bak1 |
G |
A |
17: 27,241,722 (GRCm39) |
P65L |
possibly damaging |
Het |
Cep350 |
A |
C |
1: 155,733,854 (GRCm39) |
L3013R |
probably damaging |
Het |
Clca3b |
A |
G |
3: 144,533,776 (GRCm39) |
I533T |
probably damaging |
Het |
Col6a5 |
C |
A |
9: 105,734,531 (GRCm39) |
E2637* |
probably null |
Het |
Coq5 |
G |
A |
5: 115,417,815 (GRCm39) |
R15H |
probably benign |
Het |
Dnah5 |
T |
G |
15: 28,311,424 (GRCm39) |
I1801S |
probably damaging |
Het |
Dnhd1 |
G |
A |
7: 105,352,416 (GRCm39) |
R2523Q |
probably damaging |
Het |
Dpf3 |
T |
C |
12: 83,417,370 (GRCm39) |
E34G |
probably damaging |
Het |
Dst |
C |
A |
1: 34,218,167 (GRCm39) |
Q1536K |
probably benign |
Het |
Eeig2 |
T |
C |
3: 108,892,667 (GRCm39) |
K173E |
possibly damaging |
Het |
Eng |
T |
C |
2: 32,562,971 (GRCm39) |
|
probably null |
Het |
Fignl1 |
A |
T |
11: 11,751,717 (GRCm39) |
I446N |
probably damaging |
Het |
Fras1 |
C |
A |
5: 96,784,032 (GRCm39) |
C845* |
probably null |
Het |
Gfm2 |
T |
C |
13: 97,299,401 (GRCm39) |
V347A |
probably damaging |
Het |
Gpld1 |
A |
T |
13: 25,168,053 (GRCm39) |
|
probably null |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Gsdmc4 |
C |
A |
15: 63,765,653 (GRCm39) |
V299F |
probably damaging |
Het |
Hrnr |
A |
T |
3: 93,239,450 (GRCm39) |
R3229S |
unknown |
Het |
Icam5 |
A |
G |
9: 20,946,106 (GRCm39) |
T313A |
probably benign |
Het |
Ift172 |
T |
A |
5: 31,424,958 (GRCm39) |
D668V |
possibly damaging |
Het |
Kdm5a |
T |
A |
6: 120,365,066 (GRCm39) |
C322* |
probably null |
Het |
Klk6 |
A |
G |
7: 43,478,084 (GRCm39) |
K152R |
probably benign |
Het |
Man1a2 |
A |
C |
3: 100,554,333 (GRCm39) |
I250S |
probably damaging |
Het |
Nkpd1 |
A |
G |
7: 19,257,181 (GRCm39) |
Y170C |
probably damaging |
Het |
Nmd3 |
T |
A |
3: 69,629,801 (GRCm39) |
|
probably null |
Het |
Or2y3 |
A |
G |
17: 38,393,005 (GRCm39) |
M288T |
probably benign |
Het |
Or51f1 |
A |
T |
7: 102,506,176 (GRCm39) |
D104E |
probably benign |
Het |
Pax4 |
C |
T |
6: 28,444,368 (GRCm39) |
E229K |
probably benign |
Het |
Pdc |
T |
C |
1: 150,209,105 (GRCm39) |
I196T |
possibly damaging |
Het |
Pld1 |
T |
C |
3: 28,099,230 (GRCm39) |
I299T |
probably damaging |
Het |
Pnma1 |
T |
C |
12: 84,193,819 (GRCm39) |
I295V |
probably benign |
Het |
Prkg2 |
T |
A |
5: 99,172,568 (GRCm39) |
Y49F |
probably benign |
Het |
Psmd12 |
T |
C |
11: 107,370,485 (GRCm39) |
L28P |
probably damaging |
Het |
Ptprg |
A |
G |
14: 12,154,174 (GRCm38) |
T632A |
probably benign |
Het |
Rab43 |
A |
G |
6: 87,771,637 (GRCm39) |
*118R |
probably null |
Het |
Rabep1 |
C |
T |
11: 70,795,454 (GRCm39) |
R227* |
probably null |
Het |
Rad51c |
T |
G |
11: 87,288,545 (GRCm39) |
I213L |
possibly damaging |
Het |
Ranbp17 |
A |
T |
11: 33,169,287 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,585,495 (GRCm39) |
E2735G |
probably damaging |
Het |
Sdc3 |
A |
G |
4: 130,548,995 (GRCm39) |
|
probably benign |
Het |
Sirpa |
G |
A |
2: 129,457,652 (GRCm39) |
R242H |
possibly damaging |
Het |
Slc12a4 |
G |
A |
8: 106,671,238 (GRCm39) |
T983M |
probably damaging |
Het |
Snx7 |
A |
G |
3: 117,626,506 (GRCm39) |
Y252H |
probably damaging |
Het |
St18 |
C |
T |
1: 6,887,877 (GRCm39) |
T482I |
probably benign |
Het |
St7 |
A |
G |
6: 17,846,236 (GRCm39) |
Y163C |
probably damaging |
Het |
Tas2r140 |
A |
T |
6: 40,468,866 (GRCm39) |
Q232L |
probably benign |
Het |
Tgm6 |
A |
T |
2: 129,983,222 (GRCm39) |
K270N |
probably damaging |
Het |
Tiam2 |
G |
A |
17: 3,488,996 (GRCm39) |
G768D |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,700,773 (GRCm39) |
|
probably benign |
Het |
Ube4b |
A |
C |
4: 149,465,699 (GRCm39) |
S250R |
probably null |
Het |
Ubxn2a |
G |
A |
12: 4,930,634 (GRCm39) |
A242V |
probably damaging |
Het |
Usp10 |
G |
A |
8: 120,683,420 (GRCm39) |
V764I |
possibly damaging |
Het |
Vmn1r222 |
A |
G |
13: 23,416,667 (GRCm39) |
L182P |
probably damaging |
Het |
Vmn2r114 |
A |
G |
17: 23,510,632 (GRCm39) |
V616A |
probably damaging |
Het |
Vps13a |
A |
G |
19: 16,672,863 (GRCm39) |
V1303A |
possibly damaging |
Het |
Zfp936 |
G |
A |
7: 42,839,331 (GRCm39) |
C266Y |
probably damaging |
Het |
Zscan20 |
G |
T |
4: 128,480,504 (GRCm39) |
N662K |
possibly damaging |
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 |
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 |
|
|