Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
A |
T |
16: 16,936,154 (GRCm39) |
|
probably null |
Het |
Adcy4 |
C |
T |
14: 56,016,486 (GRCm39) |
D322N |
probably damaging |
Het |
Alas1 |
A |
T |
9: 106,124,077 (GRCm39) |
L27* |
probably null |
Het |
Aldh1a7 |
A |
G |
19: 20,704,374 (GRCm39) |
V40A |
possibly damaging |
Het |
Appbp2 |
A |
T |
11: 85,085,409 (GRCm39) |
I499K |
possibly damaging |
Het |
B3gnt5 |
A |
C |
16: 19,587,894 (GRCm39) |
M38L |
probably benign |
Het |
Brd8 |
A |
G |
18: 34,747,585 (GRCm39) |
V92A |
probably damaging |
Het |
Btla |
A |
T |
16: 45,063,091 (GRCm39) |
E151D |
probably benign |
Het |
Cd79b |
T |
A |
11: 106,203,687 (GRCm39) |
T67S |
probably benign |
Het |
Cep192 |
A |
G |
18: 67,949,875 (GRCm39) |
R320G |
probably benign |
Het |
Chad |
A |
C |
11: 94,456,528 (GRCm39) |
D202A |
probably damaging |
Het |
Chil6 |
A |
G |
3: 106,295,988 (GRCm39) |
|
probably benign |
Het |
Cpz |
T |
C |
5: 35,674,748 (GRCm39) |
E167G |
possibly damaging |
Het |
Crisp2 |
T |
G |
17: 41,076,159 (GRCm39) |
H225P |
probably damaging |
Het |
Cyp2c23 |
T |
C |
19: 44,010,138 (GRCm39) |
Y69C |
possibly damaging |
Het |
Dcp1a |
T |
A |
14: 30,201,724 (GRCm39) |
L49H |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,030,672 (GRCm39) |
H3380L |
probably benign |
Het |
Dnai3 |
T |
A |
3: 145,788,820 (GRCm39) |
K254* |
probably null |
Het |
Dnm2 |
A |
G |
9: 21,415,829 (GRCm39) |
D721G |
possibly damaging |
Het |
Dnpep |
G |
T |
1: 75,293,404 (GRCm39) |
T15K |
probably benign |
Het |
Dock3 |
A |
T |
9: 106,868,354 (GRCm39) |
D643E |
probably damaging |
Het |
Ear6 |
C |
T |
14: 52,091,573 (GRCm39) |
T40I |
possibly damaging |
Het |
Fancm |
A |
G |
12: 65,137,748 (GRCm39) |
D313G |
probably damaging |
Het |
Fbxw16 |
T |
A |
9: 109,267,415 (GRCm39) |
E272V |
probably damaging |
Het |
Frmd4b |
T |
A |
6: 97,283,691 (GRCm39) |
E393D |
probably benign |
Het |
Fryl |
T |
A |
5: 73,246,473 (GRCm39) |
M1100L |
probably benign |
Het |
Gjd3 |
T |
C |
11: 102,691,247 (GRCm39) |
H252R |
probably damaging |
Het |
Gm10518 |
T |
C |
1: 179,631,477 (GRCm39) |
|
probably benign |
Het |
Gna14 |
A |
G |
19: 16,580,656 (GRCm39) |
M165V |
probably benign |
Het |
Hells |
C |
A |
19: 38,923,966 (GRCm39) |
Q72K |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,392,184 (GRCm39) |
I4031V |
probably benign |
Het |
Hspa2 |
C |
T |
12: 76,452,761 (GRCm39) |
A485V |
probably damaging |
Het |
Ighv1-54 |
T |
A |
12: 115,157,438 (GRCm39) |
I70F |
probably benign |
Het |
Il20rb |
A |
T |
9: 100,343,592 (GRCm39) |
|
probably benign |
Het |
Irag1 |
A |
G |
7: 110,487,236 (GRCm39) |
V498A |
probably damaging |
Het |
Krt1 |
C |
A |
15: 101,754,376 (GRCm39) |
V625L |
unknown |
Het |
Lamc3 |
T |
C |
2: 31,830,748 (GRCm39) |
I1495T |
probably benign |
Het |
Larp6 |
A |
G |
9: 60,645,063 (GRCm39) |
E401G |
possibly damaging |
Het |
Ldha |
A |
T |
7: 46,496,805 (GRCm39) |
H19L |
probably benign |
Het |
Lrba |
A |
G |
3: 86,192,335 (GRCm39) |
N83S |
probably damaging |
Het |
Lrp4 |
G |
T |
2: 91,316,231 (GRCm39) |
R783L |
probably benign |
Het |
Lrrk2 |
T |
G |
15: 91,687,592 (GRCm39) |
I2227S |
probably benign |
Het |
Lvrn |
T |
C |
18: 47,013,803 (GRCm39) |
L495P |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,391,548 (GRCm39) |
N1077S |
probably damaging |
Het |
Mboat1 |
A |
G |
13: 30,425,213 (GRCm39) |
T425A |
probably damaging |
Het |
Mcam |
A |
G |
9: 44,047,863 (GRCm39) |
E36G |
probably damaging |
Het |
Meis1 |
T |
A |
11: 18,966,308 (GRCm39) |
T22S |
probably benign |
Het |
Micu1 |
A |
G |
10: 59,699,076 (GRCm39) |
K451R |
possibly damaging |
Het |
Nat8 |
A |
T |
6: 85,807,505 (GRCm39) |
D209E |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,860,986 (GRCm38) |
L513M |
possibly damaging |
Het |
Nmral1 |
G |
A |
16: 4,534,274 (GRCm39) |
R56* |
probably null |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or10j27 |
A |
G |
1: 172,958,526 (GRCm39) |
V86A |
probably benign |
Het |
Or5b99 |
A |
T |
19: 12,977,195 (GRCm39) |
T282S |
probably benign |
Het |
Or5g25 |
T |
C |
2: 85,477,916 (GRCm39) |
I250V |
probably benign |
Het |
Or5h24 |
G |
A |
16: 58,919,340 (GRCm39) |
T5I |
probably damaging |
Het |
Palm3 |
A |
T |
8: 84,753,708 (GRCm39) |
R132* |
probably null |
Het |
Pax2 |
A |
G |
19: 44,804,479 (GRCm39) |
Y272C |
probably damaging |
Het |
Phc2 |
G |
A |
4: 128,616,908 (GRCm39) |
A394T |
probably benign |
Het |
Phf2 |
C |
A |
13: 48,961,198 (GRCm39) |
G831C |
unknown |
Het |
Pik3c2b |
G |
A |
1: 133,027,453 (GRCm39) |
|
probably null |
Het |
Plin2 |
T |
A |
4: 86,580,228 (GRCm39) |
I178F |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,185 (GRCm39) |
L162H |
probably damaging |
Het |
Prdm14 |
T |
A |
1: 13,192,855 (GRCm39) |
I295F |
probably damaging |
Het |
Psmd5 |
C |
T |
2: 34,760,795 (GRCm39) |
R47H |
probably benign |
Het |
Ptchd3 |
T |
A |
11: 121,733,342 (GRCm39) |
I744K |
probably damaging |
Het |
Ptrh1 |
T |
A |
2: 32,666,557 (GRCm39) |
|
probably benign |
Het |
Rab6a |
A |
G |
7: 100,277,627 (GRCm39) |
D49G |
probably damaging |
Het |
Radil |
A |
T |
5: 142,470,994 (GRCm39) |
D1062E |
probably benign |
Het |
Robo2 |
A |
G |
16: 74,149,726 (GRCm39) |
V34A |
possibly damaging |
Het |
Sall3 |
G |
A |
18: 81,014,626 (GRCm39) |
P1029S |
probably benign |
Het |
Sec14l3 |
A |
G |
11: 4,018,101 (GRCm39) |
D127G |
possibly damaging |
Het |
Sel1l2 |
A |
G |
2: 140,086,086 (GRCm39) |
Y502H |
probably damaging |
Het |
Serpina1f |
A |
G |
12: 103,656,010 (GRCm39) |
V406A |
probably damaging |
Het |
Sf3b3 |
T |
C |
8: 111,540,301 (GRCm39) |
D1040G |
probably damaging |
Het |
Sgcd |
A |
G |
11: 46,870,262 (GRCm39) |
I233T |
possibly damaging |
Het |
Slc15a3 |
A |
G |
19: 10,820,410 (GRCm39) |
Q9R |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,716,336 (GRCm39) |
F389L |
probably damaging |
Het |
Slc26a2 |
G |
T |
18: 61,331,330 (GRCm39) |
C700* |
probably null |
Het |
Slc4a7 |
A |
G |
14: 14,771,283 (GRCm38) |
Y671C |
possibly damaging |
Het |
Slc5a10 |
A |
T |
11: 61,610,708 (GRCm39) |
I22N |
probably damaging |
Het |
Slc5a9 |
C |
A |
4: 111,748,941 (GRCm39) |
|
probably null |
Het |
Slc6a12 |
A |
G |
6: 121,332,281 (GRCm39) |
D205G |
probably benign |
Het |
Tas2r115 |
G |
A |
6: 132,714,124 (GRCm39) |
H276Y |
probably damaging |
Het |
Tdpoz4 |
T |
A |
3: 93,704,318 (GRCm39) |
I205N |
probably damaging |
Het |
Tfeb |
C |
T |
17: 48,096,904 (GRCm39) |
T33I |
probably benign |
Het |
Tgm3 |
A |
G |
2: 129,890,240 (GRCm39) |
T668A |
probably benign |
Het |
Tnpo3 |
A |
G |
6: 29,582,259 (GRCm39) |
V201A |
probably benign |
Het |
Tpcn1 |
T |
A |
5: 120,694,596 (GRCm39) |
M158L |
probably benign |
Het |
Trim47 |
A |
C |
11: 115,996,918 (GRCm39) |
L612R |
probably damaging |
Het |
Trmt10c |
A |
T |
16: 55,854,438 (GRCm39) |
L399* |
probably null |
Het |
Trpm2 |
A |
T |
10: 77,753,626 (GRCm39) |
S1293T |
probably benign |
Het |
Ttn |
C |
T |
2: 76,582,941 (GRCm39) |
V22651I |
probably damaging |
Het |
Tubgcp5 |
A |
G |
7: 55,455,871 (GRCm39) |
I300V |
probably benign |
Het |
Uty |
T |
A |
Y: 1,136,883 (GRCm39) |
Q844L |
probably damaging |
Het |
Vmn2r85 |
C |
T |
10: 130,254,990 (GRCm39) |
E565K |
probably damaging |
Het |
Vmn2r97 |
T |
C |
17: 19,167,561 (GRCm39) |
V605A |
possibly damaging |
Het |
Vwa3a |
T |
C |
7: 120,375,487 (GRCm39) |
V399A |
probably damaging |
Het |
Zfp217 |
A |
G |
2: 169,961,130 (GRCm39) |
V399A |
probably damaging |
Het |
Zfp616 |
T |
A |
11: 73,974,830 (GRCm39) |
N457K |
possibly damaging |
Het |
|
Other mutations in Wnk4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Wnk4
|
APN |
11 |
101,159,574 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL00535:Wnk4
|
APN |
11 |
101,155,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Wnk4
|
APN |
11 |
101,167,509 (GRCm39) |
splice site |
probably benign |
|
IGL01931:Wnk4
|
APN |
11 |
101,159,310 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01977:Wnk4
|
APN |
11 |
101,156,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02165:Wnk4
|
APN |
11 |
101,166,117 (GRCm39) |
unclassified |
probably benign |
|
IGL02197:Wnk4
|
APN |
11 |
101,154,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02457:Wnk4
|
APN |
11 |
101,160,389 (GRCm39) |
splice site |
probably benign |
|
IGL02963:Wnk4
|
APN |
11 |
101,167,039 (GRCm39) |
unclassified |
probably benign |
|
ashamed
|
UTSW |
11 |
101,156,257 (GRCm39) |
missense |
probably damaging |
1.00 |
blushing
|
UTSW |
11 |
101,156,203 (GRCm39) |
missense |
probably damaging |
0.96 |
Caught_dead
|
UTSW |
11 |
101,155,156 (GRCm39) |
missense |
probably damaging |
1.00 |
lowered
|
UTSW |
11 |
101,159,318 (GRCm39) |
critical splice donor site |
probably null |
|
mortification
|
UTSW |
11 |
101,154,720 (GRCm39) |
makesense |
probably null |
|
shame
|
UTSW |
11 |
101,153,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Wnk4
|
UTSW |
11 |
101,156,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Wnk4
|
UTSW |
11 |
101,159,630 (GRCm39) |
missense |
probably benign |
0.01 |
R0628:Wnk4
|
UTSW |
11 |
101,165,849 (GRCm39) |
missense |
probably benign |
0.10 |
R0630:Wnk4
|
UTSW |
11 |
101,156,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R0710:Wnk4
|
UTSW |
11 |
101,164,932 (GRCm39) |
missense |
probably benign |
0.22 |
R1290:Wnk4
|
UTSW |
11 |
101,167,166 (GRCm39) |
unclassified |
probably benign |
|
R1482:Wnk4
|
UTSW |
11 |
101,160,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R1775:Wnk4
|
UTSW |
11 |
101,167,166 (GRCm39) |
unclassified |
probably benign |
|
R2005:Wnk4
|
UTSW |
11 |
101,154,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Wnk4
|
UTSW |
11 |
101,166,467 (GRCm39) |
unclassified |
probably benign |
|
R2258:Wnk4
|
UTSW |
11 |
101,165,861 (GRCm39) |
missense |
probably damaging |
0.98 |
R2323:Wnk4
|
UTSW |
11 |
101,159,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R3081:Wnk4
|
UTSW |
11 |
101,167,717 (GRCm39) |
splice site |
probably benign |
|
R3763:Wnk4
|
UTSW |
11 |
101,160,114 (GRCm39) |
missense |
probably benign |
0.00 |
R4196:Wnk4
|
UTSW |
11 |
101,160,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Wnk4
|
UTSW |
11 |
101,159,277 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4614:Wnk4
|
UTSW |
11 |
101,164,937 (GRCm39) |
missense |
probably benign |
0.00 |
R4751:Wnk4
|
UTSW |
11 |
101,167,188 (GRCm39) |
unclassified |
probably benign |
|
R5067:Wnk4
|
UTSW |
11 |
101,153,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Wnk4
|
UTSW |
11 |
101,152,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R5107:Wnk4
|
UTSW |
11 |
101,166,364 (GRCm39) |
unclassified |
probably benign |
|
R5181:Wnk4
|
UTSW |
11 |
101,156,203 (GRCm39) |
missense |
probably damaging |
0.96 |
R5205:Wnk4
|
UTSW |
11 |
101,155,964 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5252:Wnk4
|
UTSW |
11 |
101,159,574 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5273:Wnk4
|
UTSW |
11 |
101,154,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R5293:Wnk4
|
UTSW |
11 |
101,166,023 (GRCm39) |
unclassified |
probably benign |
|
R5609:Wnk4
|
UTSW |
11 |
101,166,462 (GRCm39) |
unclassified |
probably benign |
|
R5915:Wnk4
|
UTSW |
11 |
101,154,720 (GRCm39) |
makesense |
probably null |
|
R5931:Wnk4
|
UTSW |
11 |
101,152,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R6126:Wnk4
|
UTSW |
11 |
101,167,174 (GRCm39) |
unclassified |
probably benign |
|
R6164:Wnk4
|
UTSW |
11 |
101,165,894 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6191:Wnk4
|
UTSW |
11 |
101,155,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Wnk4
|
UTSW |
11 |
101,164,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Wnk4
|
UTSW |
11 |
101,156,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Wnk4
|
UTSW |
11 |
101,164,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Wnk4
|
UTSW |
11 |
101,152,026 (GRCm39) |
missense |
probably benign |
0.22 |
R7251:Wnk4
|
UTSW |
11 |
101,155,979 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7352:Wnk4
|
UTSW |
11 |
101,155,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R7404:Wnk4
|
UTSW |
11 |
101,159,318 (GRCm39) |
critical splice donor site |
probably null |
|
R7624:Wnk4
|
UTSW |
11 |
101,155,180 (GRCm39) |
nonsense |
probably null |
|
R7634:Wnk4
|
UTSW |
11 |
101,153,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Wnk4
|
UTSW |
11 |
101,160,403 (GRCm39) |
missense |
probably damaging |
0.96 |
R8006:Wnk4
|
UTSW |
11 |
101,159,182 (GRCm39) |
missense |
probably benign |
0.00 |
R8046:Wnk4
|
UTSW |
11 |
101,164,918 (GRCm39) |
missense |
probably benign |
0.20 |
R8143:Wnk4
|
UTSW |
11 |
101,153,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Wnk4
|
UTSW |
11 |
101,166,147 (GRCm39) |
nonsense |
probably null |
|
R8735:Wnk4
|
UTSW |
11 |
101,167,092 (GRCm39) |
missense |
unknown |
|
R9025:Wnk4
|
UTSW |
11 |
101,153,641 (GRCm39) |
nonsense |
probably null |
|
R9206:Wnk4
|
UTSW |
11 |
101,164,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Wnk4
|
UTSW |
11 |
101,160,078 (GRCm39) |
missense |
probably damaging |
0.98 |
R9610:Wnk4
|
UTSW |
11 |
101,159,250 (GRCm39) |
nonsense |
probably null |
|
R9611:Wnk4
|
UTSW |
11 |
101,159,250 (GRCm39) |
nonsense |
probably null |
|
R9674:Wnk4
|
UTSW |
11 |
101,166,874 (GRCm39) |
missense |
unknown |
|
|