Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013G24Rik |
A |
T |
4: 137,182,535 (GRCm39) |
N230I |
possibly damaging |
Het |
4933427D14Rik |
G |
T |
11: 72,060,609 (GRCm39) |
Q687K |
probably damaging |
Het |
Actrt2 |
A |
G |
4: 154,751,869 (GRCm39) |
L89P |
probably damaging |
Het |
Adamts1 |
A |
C |
16: 85,599,260 (GRCm39) |
S113R |
probably benign |
Het |
Agxt2 |
G |
T |
15: 10,373,948 (GRCm39) |
C118F |
probably damaging |
Het |
Akap8 |
G |
A |
17: 32,536,266 (GRCm39) |
T49I |
probably benign |
Het |
Alk |
A |
T |
17: 72,176,748 (GRCm39) |
W1519R |
probably damaging |
Het |
Atf7ip |
T |
A |
6: 136,536,803 (GRCm39) |
F12Y |
probably damaging |
Het |
Atp13a5 |
A |
G |
16: 29,167,558 (GRCm39) |
C131R |
probably damaging |
Het |
Atp8b4 |
A |
G |
2: 126,269,283 (GRCm39) |
L168P |
probably damaging |
Het |
Blm |
G |
T |
7: 80,155,641 (GRCm39) |
S346* |
probably null |
Het |
Ccnt2 |
T |
G |
1: 127,727,182 (GRCm39) |
C199G |
probably damaging |
Het |
Cd151 |
A |
T |
7: 141,050,504 (GRCm39) |
H219L |
probably damaging |
Het |
Cd200r2 |
A |
T |
16: 44,735,410 (GRCm39) |
R248S |
probably damaging |
Het |
Cdh3 |
A |
G |
8: 107,282,078 (GRCm39) |
D822G |
possibly damaging |
Het |
Clec4b1 |
T |
C |
6: 123,046,729 (GRCm39) |
|
probably null |
Het |
Cluh |
C |
A |
11: 74,556,812 (GRCm39) |
L951I |
probably benign |
Het |
Cog7 |
A |
T |
7: 121,562,494 (GRCm39) |
|
probably null |
Het |
Col25a1 |
C |
A |
3: 130,270,043 (GRCm39) |
P197Q |
probably damaging |
Het |
Csde1 |
T |
A |
3: 102,963,742 (GRCm39) |
S636R |
possibly damaging |
Het |
Ect2l |
C |
A |
10: 18,075,688 (GRCm39) |
C66F |
possibly damaging |
Het |
Elac2 |
T |
C |
11: 64,890,262 (GRCm39) |
M671T |
probably benign |
Het |
Evi5 |
T |
C |
5: 107,969,614 (GRCm39) |
N143S |
probably benign |
Het |
Ext2 |
A |
G |
2: 93,636,430 (GRCm39) |
V228A |
probably damaging |
Het |
Fbxo38 |
A |
G |
18: 62,639,051 (GRCm39) |
Y1084H |
probably damaging |
Het |
Fcgr4 |
T |
A |
1: 170,856,760 (GRCm39) |
L209Q |
probably damaging |
Het |
Fgd3 |
C |
T |
13: 49,450,000 (GRCm39) |
S83N |
probably benign |
Het |
Gigyf2 |
T |
A |
1: 87,349,215 (GRCm39) |
M664K |
probably benign |
Het |
Il27ra |
A |
T |
8: 84,766,128 (GRCm39) |
S219T |
probably benign |
Het |
Itprid2 |
A |
G |
2: 79,487,690 (GRCm39) |
D591G |
probably benign |
Het |
Kif15 |
T |
C |
9: 122,826,862 (GRCm39) |
V800A |
probably damaging |
Het |
Lmo7 |
T |
A |
14: 102,137,996 (GRCm39) |
D666E |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,678,295 (GRCm39) |
D520G |
probably damaging |
Het |
Lrriq3 |
T |
A |
3: 154,893,934 (GRCm39) |
M545K |
probably benign |
Het |
Lsm5 |
T |
A |
6: 56,680,310 (GRCm39) |
D44V |
probably damaging |
Het |
Man1c1 |
G |
T |
4: 134,296,379 (GRCm39) |
Y430* |
probably null |
Het |
Map4 |
T |
A |
9: 109,866,346 (GRCm39) |
|
probably null |
Het |
Megf6 |
A |
G |
4: 154,343,398 (GRCm39) |
K561R |
probably benign |
Het |
Myo1e |
T |
C |
9: 70,229,680 (GRCm39) |
Y173H |
probably damaging |
Het |
Myo6 |
T |
A |
9: 80,190,823 (GRCm39) |
S791R |
possibly damaging |
Het |
Nol11 |
C |
A |
11: 107,075,597 (GRCm39) |
E144* |
probably null |
Het |
Ntng2 |
C |
T |
2: 29,087,074 (GRCm39) |
R416Q |
probably damaging |
Het |
Nxpe3 |
T |
A |
16: 55,686,880 (GRCm39) |
I43F |
possibly damaging |
Het |
Or4g17 |
T |
A |
2: 111,209,837 (GRCm39) |
V164E |
possibly damaging |
Het |
Or5t5 |
A |
T |
2: 86,616,691 (GRCm39) |
T206S |
possibly damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,808,999 (GRCm39) |
I64V |
probably damaging |
Het |
Prf1 |
G |
A |
10: 61,136,033 (GRCm39) |
R103H |
probably benign |
Het |
Rest |
A |
G |
5: 77,428,874 (GRCm39) |
D431G |
probably damaging |
Het |
Serpina10 |
A |
T |
12: 103,583,127 (GRCm39) |
L439Q |
probably damaging |
Het |
Sgk3 |
T |
G |
1: 9,951,804 (GRCm39) |
V176G |
probably damaging |
Het |
Slc19a3 |
A |
G |
1: 83,000,454 (GRCm39) |
S188P |
probably damaging |
Het |
Sorbs1 |
A |
G |
19: 40,338,392 (GRCm39) |
I336T |
probably damaging |
Het |
Strip1 |
C |
T |
3: 107,527,355 (GRCm39) |
|
probably null |
Het |
Syt4 |
T |
C |
18: 31,576,799 (GRCm39) |
E185G |
possibly damaging |
Het |
Tcaf3 |
T |
A |
6: 42,566,738 (GRCm39) |
I784F |
probably damaging |
Het |
Tgfbr3l |
G |
T |
8: 4,299,439 (GRCm39) |
R74L |
possibly damaging |
Het |
Thoc7 |
A |
G |
14: 13,949,282 (GRCm38) |
M194T |
probably benign |
Het |
Thsd7b |
T |
C |
1: 129,879,129 (GRCm39) |
Y989H |
probably damaging |
Het |
Tmem156 |
C |
T |
5: 65,233,161 (GRCm39) |
V134I |
probably benign |
Het |
Tnks |
A |
T |
8: 35,320,457 (GRCm39) |
V738E |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,770,240 (GRCm39) |
I342F |
probably damaging |
Het |
Vmn2r69 |
A |
T |
7: 85,060,711 (GRCm39) |
V291D |
probably damaging |
Het |
Wdr59 |
GGGTGGTG |
GGGTG |
8: 112,207,172 (GRCm39) |
|
probably benign |
Het |
Yes1 |
T |
A |
5: 32,812,584 (GRCm39) |
C285S |
probably benign |
Het |
Zbed6 |
T |
C |
1: 133,586,472 (GRCm39) |
I288M |
probably damaging |
Het |
Zbtb49 |
T |
C |
5: 38,371,263 (GRCm39) |
N206S |
probably benign |
Het |
|
Other mutations in Wnk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00901:Wnk1
|
APN |
6 |
119,937,669 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01364:Wnk1
|
APN |
6 |
119,914,372 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01715:Wnk1
|
APN |
6 |
119,925,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Wnk1
|
APN |
6 |
119,940,446 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02043:Wnk1
|
APN |
6 |
119,926,039 (GRCm39) |
unclassified |
probably benign |
|
IGL02268:Wnk1
|
APN |
6 |
119,914,334 (GRCm39) |
nonsense |
probably null |
|
IGL02348:Wnk1
|
APN |
6 |
119,940,289 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02425:Wnk1
|
APN |
6 |
119,940,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02850:Wnk1
|
APN |
6 |
119,914,823 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03160:Wnk1
|
APN |
6 |
119,903,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03387:Wnk1
|
APN |
6 |
119,931,148 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03405:Wnk1
|
APN |
6 |
119,930,856 (GRCm39) |
missense |
probably benign |
0.41 |
Actor
|
UTSW |
6 |
119,947,939 (GRCm39) |
missense |
probably damaging |
1.00 |
Bad
|
UTSW |
6 |
119,942,639 (GRCm39) |
intron |
probably benign |
|
Blink
|
UTSW |
6 |
119,979,234 (GRCm39) |
nonsense |
probably null |
|
Knock
|
UTSW |
6 |
119,920,839 (GRCm39) |
splice site |
probably null |
|
Narrow
|
UTSW |
6 |
119,969,369 (GRCm39) |
missense |
probably damaging |
1.00 |
nictitate
|
UTSW |
6 |
119,979,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
opportunity
|
UTSW |
6 |
119,928,029 (GRCm39) |
missense |
probably damaging |
1.00 |
path
|
UTSW |
6 |
120,014,110 (GRCm39) |
missense |
probably damaging |
0.99 |
Stormy
|
UTSW |
6 |
119,969,408 (GRCm39) |
missense |
probably damaging |
1.00 |
tear
|
UTSW |
6 |
119,940,431 (GRCm39) |
missense |
probably damaging |
0.98 |
Tic
|
UTSW |
6 |
119,927,044 (GRCm39) |
missense |
probably damaging |
1.00 |
Unforgiving
|
UTSW |
6 |
119,925,243 (GRCm39) |
missense |
probably damaging |
1.00 |
Window
|
UTSW |
6 |
119,969,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Woke
|
UTSW |
6 |
119,939,916 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03052:Wnk1
|
UTSW |
6 |
119,921,760 (GRCm39) |
splice site |
probably benign |
|
PIT4480001:Wnk1
|
UTSW |
6 |
119,940,328 (GRCm39) |
nonsense |
probably null |
|
R0044:Wnk1
|
UTSW |
6 |
120,014,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R0207:Wnk1
|
UTSW |
6 |
119,929,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R0333:Wnk1
|
UTSW |
6 |
119,905,124 (GRCm39) |
intron |
probably benign |
|
R0453:Wnk1
|
UTSW |
6 |
119,940,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:Wnk1
|
UTSW |
6 |
119,946,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R0501:Wnk1
|
UTSW |
6 |
119,939,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Wnk1
|
UTSW |
6 |
119,903,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Wnk1
|
UTSW |
6 |
119,903,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Wnk1
|
UTSW |
6 |
119,925,466 (GRCm39) |
missense |
probably damaging |
0.98 |
R1148:Wnk1
|
UTSW |
6 |
119,928,967 (GRCm39) |
splice site |
probably benign |
|
R1188:Wnk1
|
UTSW |
6 |
119,925,670 (GRCm39) |
nonsense |
probably null |
|
R1245:Wnk1
|
UTSW |
6 |
119,925,418 (GRCm39) |
missense |
probably benign |
0.26 |
R1449:Wnk1
|
UTSW |
6 |
119,929,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Wnk1
|
UTSW |
6 |
119,927,645 (GRCm39) |
splice site |
probably benign |
|
R1869:Wnk1
|
UTSW |
6 |
119,928,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Wnk1
|
UTSW |
6 |
119,928,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Wnk1
|
UTSW |
6 |
119,929,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Wnk1
|
UTSW |
6 |
119,946,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R1961:Wnk1
|
UTSW |
6 |
119,946,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R1964:Wnk1
|
UTSW |
6 |
119,911,343 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1983:Wnk1
|
UTSW |
6 |
119,914,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Wnk1
|
UTSW |
6 |
119,905,118 (GRCm39) |
splice site |
probably null |
|
R2144:Wnk1
|
UTSW |
6 |
119,925,949 (GRCm39) |
unclassified |
probably benign |
|
R2186:Wnk1
|
UTSW |
6 |
119,925,528 (GRCm39) |
missense |
probably benign |
0.26 |
R2281:Wnk1
|
UTSW |
6 |
119,940,601 (GRCm39) |
splice site |
probably null |
|
R2338:Wnk1
|
UTSW |
6 |
119,946,495 (GRCm39) |
missense |
probably benign |
0.42 |
R2420:Wnk1
|
UTSW |
6 |
119,913,328 (GRCm39) |
critical splice donor site |
probably null |
|
R3727:Wnk1
|
UTSW |
6 |
119,969,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Wnk1
|
UTSW |
6 |
119,979,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3836:Wnk1
|
UTSW |
6 |
119,927,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R3837:Wnk1
|
UTSW |
6 |
119,927,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Wnk1
|
UTSW |
6 |
119,946,315 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3903:Wnk1
|
UTSW |
6 |
119,926,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Wnk1
|
UTSW |
6 |
119,928,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R4095:Wnk1
|
UTSW |
6 |
119,925,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4232:Wnk1
|
UTSW |
6 |
119,926,222 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4422:Wnk1
|
UTSW |
6 |
119,930,856 (GRCm39) |
missense |
probably benign |
0.41 |
R4423:Wnk1
|
UTSW |
6 |
119,903,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4572:Wnk1
|
UTSW |
6 |
119,928,872 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4704:Wnk1
|
UTSW |
6 |
119,942,705 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4755:Wnk1
|
UTSW |
6 |
119,940,431 (GRCm39) |
missense |
probably damaging |
0.98 |
R4812:Wnk1
|
UTSW |
6 |
119,929,732 (GRCm39) |
missense |
probably benign |
0.16 |
R4822:Wnk1
|
UTSW |
6 |
119,939,399 (GRCm39) |
missense |
probably benign |
0.02 |
R4879:Wnk1
|
UTSW |
6 |
119,926,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Wnk1
|
UTSW |
6 |
119,942,696 (GRCm39) |
intron |
probably benign |
|
R5002:Wnk1
|
UTSW |
6 |
119,914,924 (GRCm39) |
missense |
probably benign |
0.13 |
R5037:Wnk1
|
UTSW |
6 |
119,942,696 (GRCm39) |
intron |
probably benign |
|
R5152:Wnk1
|
UTSW |
6 |
119,979,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5257:Wnk1
|
UTSW |
6 |
120,014,149 (GRCm39) |
missense |
probably benign |
0.00 |
R5354:Wnk1
|
UTSW |
6 |
119,945,484 (GRCm39) |
missense |
probably benign |
0.01 |
R5421:Wnk1
|
UTSW |
6 |
119,929,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5564:Wnk1
|
UTSW |
6 |
119,925,852 (GRCm39) |
unclassified |
probably benign |
|
R5600:Wnk1
|
UTSW |
6 |
119,926,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Wnk1
|
UTSW |
6 |
119,969,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6083:Wnk1
|
UTSW |
6 |
120,014,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R6110:Wnk1
|
UTSW |
6 |
119,949,958 (GRCm39) |
intron |
probably benign |
|
R6128:Wnk1
|
UTSW |
6 |
119,940,747 (GRCm39) |
splice site |
probably null |
|
R6237:Wnk1
|
UTSW |
6 |
119,929,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Wnk1
|
UTSW |
6 |
119,925,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Wnk1
|
UTSW |
6 |
119,939,916 (GRCm39) |
missense |
probably benign |
0.12 |
R6696:Wnk1
|
UTSW |
6 |
119,925,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Wnk1
|
UTSW |
6 |
119,925,742 (GRCm39) |
missense |
probably benign |
0.26 |
R6923:Wnk1
|
UTSW |
6 |
119,942,639 (GRCm39) |
intron |
probably benign |
|
R7024:Wnk1
|
UTSW |
6 |
119,942,687 (GRCm39) |
intron |
probably benign |
|
R7072:Wnk1
|
UTSW |
6 |
119,914,822 (GRCm39) |
missense |
unknown |
|
R7087:Wnk1
|
UTSW |
6 |
120,014,491 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7102:Wnk1
|
UTSW |
6 |
119,925,268 (GRCm39) |
missense |
unknown |
|
R7134:Wnk1
|
UTSW |
6 |
119,903,389 (GRCm39) |
missense |
unknown |
|
R7137:Wnk1
|
UTSW |
6 |
120,015,173 (GRCm39) |
unclassified |
probably benign |
|
R7142:Wnk1
|
UTSW |
6 |
119,926,240 (GRCm39) |
missense |
probably benign |
0.09 |
R7174:Wnk1
|
UTSW |
6 |
119,947,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Wnk1
|
UTSW |
6 |
119,920,839 (GRCm39) |
splice site |
probably null |
|
R7218:Wnk1
|
UTSW |
6 |
119,979,234 (GRCm39) |
nonsense |
probably null |
|
R7498:Wnk1
|
UTSW |
6 |
119,904,157 (GRCm39) |
missense |
unknown |
|
R7599:Wnk1
|
UTSW |
6 |
119,906,789 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7615:Wnk1
|
UTSW |
6 |
119,909,699 (GRCm39) |
missense |
probably benign |
0.27 |
R7799:Wnk1
|
UTSW |
6 |
119,926,137 (GRCm39) |
missense |
probably benign |
0.04 |
R7979:Wnk1
|
UTSW |
6 |
120,014,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R8075:Wnk1
|
UTSW |
6 |
119,909,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R8331:Wnk1
|
UTSW |
6 |
119,930,794 (GRCm39) |
missense |
probably benign |
0.09 |
R8343:Wnk1
|
UTSW |
6 |
119,940,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R8348:Wnk1
|
UTSW |
6 |
119,906,960 (GRCm39) |
splice site |
probably null |
|
R8359:Wnk1
|
UTSW |
6 |
119,969,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Wnk1
|
UTSW |
6 |
119,911,388 (GRCm39) |
missense |
unknown |
|
R8519:Wnk1
|
UTSW |
6 |
119,927,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R8930:Wnk1
|
UTSW |
6 |
119,940,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R8932:Wnk1
|
UTSW |
6 |
119,940,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R8933:Wnk1
|
UTSW |
6 |
120,013,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Wnk1
|
UTSW |
6 |
119,939,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Wnk1
|
UTSW |
6 |
119,925,631 (GRCm39) |
missense |
unknown |
|
R9148:Wnk1
|
UTSW |
6 |
119,925,631 (GRCm39) |
missense |
unknown |
|
R9354:Wnk1
|
UTSW |
6 |
119,942,660 (GRCm39) |
missense |
unknown |
|
R9379:Wnk1
|
UTSW |
6 |
119,928,678 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Wnk1
|
UTSW |
6 |
120,013,993 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Wnk1
|
UTSW |
6 |
119,925,166 (GRCm39) |
missense |
unknown |
|
|