Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,772,766 (GRCm39) |
F652I |
probably damaging |
Het |
Adam17 |
A |
T |
12: 21,386,665 (GRCm39) |
I457K |
probably benign |
Het |
Arpin |
T |
C |
7: 79,585,038 (GRCm39) |
|
probably benign |
Het |
Bhlhe40 |
A |
G |
6: 108,638,467 (GRCm39) |
E51G |
probably benign |
Het |
Ces1a |
C |
T |
8: 93,766,156 (GRCm39) |
D153N |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,536,200 (GRCm39) |
M547V |
probably benign |
Het |
Csrnp2 |
C |
T |
15: 100,386,067 (GRCm39) |
R57K |
possibly damaging |
Het |
Dact1 |
A |
T |
12: 71,365,619 (GRCm39) |
K763M |
probably damaging |
Het |
Ddost |
A |
T |
4: 138,035,583 (GRCm39) |
I101F |
possibly damaging |
Het |
Dyrk1b |
C |
T |
7: 27,882,028 (GRCm39) |
R130W |
probably damaging |
Het |
Ep400 |
A |
C |
5: 110,824,315 (GRCm39) |
|
probably null |
Het |
Fam227a |
A |
G |
15: 79,501,978 (GRCm39) |
V532A |
probably benign |
Het |
Flnc |
C |
A |
6: 29,460,736 (GRCm39) |
T2609K |
probably damaging |
Het |
Gbp10 |
A |
G |
5: 105,372,256 (GRCm39) |
V168A |
probably benign |
Het |
Gp5 |
A |
G |
16: 30,127,057 (GRCm39) |
V539A |
probably benign |
Het |
H2-T13 |
T |
A |
17: 36,392,375 (GRCm39) |
R33S |
unknown |
Het |
Itih5 |
A |
G |
2: 10,195,013 (GRCm39) |
E135G |
probably benign |
Het |
L2hgdh |
A |
G |
12: 69,739,172 (GRCm39) |
V433A |
probably benign |
Het |
Leng9 |
A |
G |
7: 4,152,263 (GRCm39) |
S138P |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Ly6g6e |
T |
C |
17: 35,296,159 (GRCm39) |
V10A |
probably benign |
Het |
Lypla1 |
C |
T |
1: 4,911,248 (GRCm39) |
P178S |
probably benign |
Het |
Mark1 |
A |
G |
1: 184,651,858 (GRCm39) |
F216L |
possibly damaging |
Het |
Mertk |
G |
A |
2: 128,624,527 (GRCm39) |
R646Q |
possibly damaging |
Het |
Mmp9 |
A |
C |
2: 164,791,235 (GRCm39) |
D135A |
probably benign |
Het |
Nefl |
A |
G |
14: 68,324,849 (GRCm39) |
K529E |
unknown |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nwd1 |
A |
G |
8: 73,421,917 (GRCm39) |
T988A |
probably damaging |
Het |
P4ha2 |
T |
A |
11: 54,022,065 (GRCm39) |
C529* |
probably null |
Het |
Pcdhb4 |
T |
A |
18: 37,441,417 (GRCm39) |
F242L |
probably damaging |
Het |
Pced1b |
A |
G |
15: 97,282,450 (GRCm39) |
N163S |
probably damaging |
Het |
Pde8b |
A |
G |
13: 95,169,369 (GRCm39) |
V585A |
probably damaging |
Het |
Pknox2 |
T |
A |
9: 36,804,252 (GRCm39) |
T432S |
probably damaging |
Het |
Rad18 |
A |
G |
6: 112,658,298 (GRCm39) |
|
probably null |
Het |
Rpgrip1l |
C |
T |
8: 91,996,886 (GRCm39) |
V665I |
probably benign |
Het |
Rreb1 |
A |
G |
13: 38,114,734 (GRCm39) |
I698V |
probably benign |
Het |
Schip1 |
TCTGGCC |
TC |
3: 68,525,060 (GRCm39) |
|
probably null |
Het |
Slc2a4 |
C |
T |
11: 69,837,450 (GRCm39) |
V32M |
probably damaging |
Het |
Slc40a1 |
A |
G |
1: 45,950,499 (GRCm39) |
Y318H |
probably damaging |
Het |
Spag16 |
A |
G |
1: 69,897,717 (GRCm39) |
T156A |
probably benign |
Het |
Srebf1 |
C |
A |
11: 60,097,868 (GRCm39) |
A103S |
probably benign |
Het |
Sspn |
C |
T |
6: 145,899,334 (GRCm39) |
|
probably benign |
Het |
Stoml2 |
A |
T |
4: 43,030,238 (GRCm39) |
|
probably null |
Het |
Stra6 |
T |
A |
9: 58,054,770 (GRCm39) |
V319E |
probably damaging |
Het |
Syt7 |
T |
C |
19: 10,416,780 (GRCm39) |
F414L |
probably damaging |
Het |
Tet3 |
G |
T |
6: 83,381,226 (GRCm39) |
P314Q |
probably damaging |
Het |
Tnrc18 |
A |
T |
5: 142,757,128 (GRCm39) |
L1313Q |
|
Het |
Topors |
A |
T |
4: 40,260,460 (GRCm39) |
D941E |
unknown |
Het |
Txnip |
T |
A |
3: 96,465,659 (GRCm39) |
C36* |
probably null |
Het |
Uba3 |
A |
T |
6: 97,168,491 (GRCm39) |
M178K |
probably damaging |
Het |
Vmn1r6 |
A |
G |
6: 56,979,925 (GRCm39) |
T196A |
probably benign |
Het |
Vwc2 |
T |
A |
11: 11,066,129 (GRCm39) |
S72R |
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 |
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 |
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 |
|
|