Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
A |
11: 110,110,526 (GRCm39) |
Y541F |
probably damaging |
Het |
Acot12 |
T |
A |
13: 91,911,083 (GRCm39) |
V136E |
probably benign |
Het |
Aftph |
A |
G |
11: 20,648,311 (GRCm39) |
|
probably null |
Het |
Ambra1 |
C |
T |
2: 91,603,039 (GRCm39) |
|
probably benign |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ano9 |
T |
C |
7: 140,690,415 (GRCm39) |
D73G |
probably benign |
Het |
Asap3 |
G |
A |
4: 135,969,975 (GRCm39) |
D778N |
probably benign |
Het |
Atp8a2 |
G |
T |
14: 60,245,918 (GRCm39) |
Y591* |
probably null |
Het |
Blk |
T |
C |
14: 63,613,414 (GRCm39) |
T365A |
probably benign |
Het |
C4b |
G |
T |
17: 34,962,621 (GRCm39) |
S27Y |
probably damaging |
Het |
C6 |
G |
T |
15: 4,833,129 (GRCm39) |
|
probably null |
Het |
Ccdc33 |
T |
A |
9: 57,974,839 (GRCm39) |
I345F |
possibly damaging |
Het |
Cetn3 |
T |
A |
13: 81,940,268 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
T |
A |
6: 102,244,389 (GRCm39) |
I387L |
possibly damaging |
Het |
Cog8 |
A |
G |
8: 107,782,984 (GRCm39) |
C102R |
probably damaging |
Het |
Cspg4b |
T |
C |
13: 113,456,321 (GRCm39) |
I789T |
probably benign |
Het |
Cyp2c55 |
CA |
C |
19: 39,030,522 (GRCm39) |
|
probably null |
Het |
Defa40 |
T |
A |
8: 21,740,380 (GRCm39) |
L62Q |
probably damaging |
Het |
Dmxl1 |
C |
T |
18: 50,022,534 (GRCm39) |
A1624V |
probably damaging |
Het |
Dnah1 |
T |
G |
14: 31,022,705 (GRCm39) |
E1144A |
possibly damaging |
Het |
Dnah12 |
T |
A |
14: 26,439,201 (GRCm39) |
|
probably null |
Het |
Dnah2 |
G |
A |
11: 69,367,517 (GRCm39) |
T1794I |
probably damaging |
Het |
Entrep1 |
T |
C |
19: 23,953,019 (GRCm39) |
|
probably null |
Het |
Erbin |
A |
T |
13: 103,971,282 (GRCm39) |
M778K |
probably benign |
Het |
Fbxw10 |
G |
T |
11: 62,738,573 (GRCm39) |
A156S |
probably damaging |
Het |
Flnc |
T |
A |
6: 29,460,805 (GRCm39) |
F2632Y |
probably damaging |
Het |
Frmd4a |
A |
G |
2: 4,534,628 (GRCm39) |
K160E |
probably damaging |
Het |
Glipr1l2 |
A |
G |
10: 111,943,029 (GRCm39) |
K295E |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,370,119 (GRCm39) |
C465* |
probably null |
Het |
Hoxb4 |
A |
G |
11: 96,211,014 (GRCm39) |
I205V |
probably damaging |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Il36a |
A |
G |
2: 24,106,032 (GRCm39) |
N29S |
probably benign |
Het |
Ilk |
A |
G |
7: 105,391,011 (GRCm39) |
S292G |
probably benign |
Het |
Itgb5 |
G |
C |
16: 33,696,348 (GRCm39) |
G180R |
probably damaging |
Het |
Josd1-ps |
T |
C |
7: 27,648,768 (GRCm39) |
|
noncoding transcript |
Het |
Kcnip4 |
T |
C |
5: 48,567,207 (GRCm39) |
D120G |
possibly damaging |
Het |
Kin |
A |
G |
2: 10,085,455 (GRCm39) |
D5G |
probably benign |
Het |
Lrrtm2 |
C |
A |
18: 35,346,372 (GRCm39) |
G310V |
probably damaging |
Het |
Med1 |
T |
C |
11: 98,046,186 (GRCm39) |
|
probably benign |
Het |
Mepce |
C |
A |
5: 137,783,544 (GRCm39) |
|
probably benign |
Het |
Nckipsd |
T |
A |
9: 108,691,114 (GRCm39) |
|
probably benign |
Het |
Notch3 |
T |
A |
17: 32,366,937 (GRCm39) |
Q866L |
probably benign |
Het |
Or52b4 |
A |
T |
7: 102,183,962 (GRCm39) |
T3S |
probably benign |
Het |
Or5l14 |
A |
T |
2: 87,793,040 (GRCm39) |
H65Q |
possibly damaging |
Het |
Or8k20 |
A |
T |
2: 86,106,107 (GRCm39) |
C241* |
probably null |
Het |
Orai1 |
T |
C |
5: 123,149,894 (GRCm39) |
|
probably benign |
Het |
Pate12 |
G |
A |
9: 36,344,089 (GRCm39) |
C24Y |
probably damaging |
Het |
Pcdhb8 |
A |
T |
18: 37,489,219 (GRCm39) |
E299V |
probably damaging |
Het |
Pcnx4 |
G |
A |
12: 72,613,959 (GRCm39) |
D635N |
probably damaging |
Het |
Pex5 |
T |
C |
6: 124,375,322 (GRCm39) |
I567V |
probably benign |
Het |
Ppfibp2 |
T |
C |
7: 107,328,390 (GRCm39) |
S485P |
probably benign |
Het |
Sbno1 |
T |
C |
5: 124,542,087 (GRCm39) |
Y356C |
probably damaging |
Het |
Sdcbp |
T |
C |
4: 6,381,056 (GRCm39) |
I67T |
possibly damaging |
Het |
Slc5a7 |
A |
G |
17: 54,583,679 (GRCm39) |
I537T |
probably benign |
Het |
Slc66a1 |
A |
T |
4: 139,029,095 (GRCm39) |
|
probably null |
Het |
Smad4 |
A |
G |
18: 73,774,974 (GRCm39) |
C442R |
probably damaging |
Het |
Smpd5 |
A |
G |
15: 76,179,070 (GRCm39) |
H146R |
possibly damaging |
Het |
Snai2 |
A |
G |
16: 14,524,605 (GRCm39) |
Y37C |
probably benign |
Het |
Snapc4 |
C |
T |
2: 26,256,004 (GRCm39) |
S840N |
possibly damaging |
Het |
Stpg2 |
T |
C |
3: 138,921,134 (GRCm39) |
I113T |
probably benign |
Het |
Tbc1d32 |
T |
C |
10: 55,925,125 (GRCm39) |
|
probably null |
Het |
Tfg |
A |
T |
16: 56,521,520 (GRCm39) |
S39R |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 130,116,236 (GRCm39) |
S1330T |
possibly damaging |
Het |
Tnfaip3 |
T |
C |
10: 18,881,321 (GRCm39) |
T322A |
probably benign |
Het |
Tpra1 |
A |
G |
6: 88,888,691 (GRCm39) |
Y291C |
probably damaging |
Het |
Trcg1 |
A |
G |
9: 57,154,003 (GRCm39) |
D658G |
probably damaging |
Het |
Trip4 |
C |
T |
9: 65,782,304 (GRCm39) |
V143I |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,033,084 (GRCm39) |
K1691E |
probably damaging |
Het |
Ttc8 |
T |
A |
12: 98,908,562 (GRCm39) |
M77K |
possibly damaging |
Het |
Tubb2a |
A |
T |
13: 34,258,572 (GRCm39) |
M406K |
probably benign |
Het |
Txnrd1 |
T |
A |
10: 82,717,751 (GRCm39) |
|
probably null |
Het |
Ugt2a3 |
C |
A |
5: 87,479,144 (GRCm39) |
R268L |
probably benign |
Het |
Usp34 |
T |
G |
11: 23,323,410 (GRCm39) |
M982R |
possibly damaging |
Het |
Vmn2r43 |
T |
A |
7: 8,258,102 (GRCm39) |
K370N |
probably benign |
Het |
Vopp1 |
A |
T |
6: 57,739,355 (GRCm39) |
|
probably benign |
Het |
Vps11 |
A |
C |
9: 44,264,597 (GRCm39) |
C660G |
probably benign |
Het |
Wtap |
A |
G |
17: 13,188,322 (GRCm39) |
Y193H |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,009,444 (GRCm39) |
V470D |
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 |
R0526:Wnk1
|
UTSW |
6 |
119,928,953 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|
|