Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy7 |
G |
A |
8: 89,054,336 (GRCm39) |
G1064R |
probably damaging |
Het |
Adcy9 |
A |
G |
16: 4,106,687 (GRCm39) |
V1046A |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,570,247 (GRCm39) |
|
probably null |
Het |
Apbb2 |
A |
C |
5: 66,469,507 (GRCm39) |
L554W |
probably damaging |
Het |
Arhgef10 |
C |
T |
8: 15,024,993 (GRCm39) |
P722S |
probably damaging |
Het |
B3galt9 |
A |
T |
2: 34,729,209 (GRCm39) |
Y336F |
probably damaging |
Het |
Capns1 |
A |
C |
7: 29,893,510 (GRCm39) |
M1R |
probably null |
Het |
Chst1 |
C |
T |
2: 92,443,761 (GRCm39) |
Q78* |
probably null |
Het |
Clec12b |
A |
G |
6: 129,356,580 (GRCm39) |
S195P |
possibly damaging |
Het |
Cog8 |
C |
T |
8: 107,779,208 (GRCm39) |
M356I |
probably damaging |
Het |
Cyp4b1 |
T |
C |
4: 115,482,424 (GRCm39) |
N452D |
probably damaging |
Het |
Defb40 |
A |
T |
8: 19,024,994 (GRCm39) |
Y71N |
probably benign |
Het |
Dhx8 |
G |
T |
11: 101,629,021 (GRCm39) |
R190L |
|
Het |
Disp1 |
G |
A |
1: 182,868,799 (GRCm39) |
T1207M |
possibly damaging |
Het |
Dnah9 |
T |
A |
11: 66,008,464 (GRCm39) |
Y787F |
probably benign |
Het |
Egflam |
T |
C |
15: 7,237,155 (GRCm39) |
N1010D |
probably damaging |
Het |
Fam151a |
T |
A |
4: 106,603,254 (GRCm39) |
Y272N |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,492,938 (GRCm39) |
Y3887H |
probably damaging |
Het |
Fpr3 |
T |
A |
17: 18,191,725 (GRCm39) |
I332N |
probably benign |
Het |
Frmd4a |
G |
T |
2: 4,608,765 (GRCm39) |
G878W |
probably damaging |
Het |
Fv1 |
T |
C |
4: 147,953,628 (GRCm39) |
Y65H |
possibly damaging |
Het |
Gabra6 |
G |
A |
11: 42,198,289 (GRCm39) |
A387V |
probably benign |
Het |
Gna11 |
T |
C |
10: 81,366,715 (GRCm39) |
T332A |
|
Het |
Gpr161 |
T |
A |
1: 165,133,757 (GRCm39) |
H6Q |
possibly damaging |
Het |
Grin2b |
CA |
C |
6: 135,709,509 (GRCm39) |
|
probably null |
Het |
Heatr3 |
A |
T |
8: 88,876,827 (GRCm39) |
M290L |
probably benign |
Het |
Ifi47 |
T |
G |
11: 48,986,842 (GRCm39) |
I203R |
probably benign |
Het |
Ighv5-8 |
TATACAT |
TAT |
12: 113,618,583 (GRCm39) |
|
probably benign |
Het |
Klhl10 |
A |
G |
11: 100,337,962 (GRCm39) |
M234V |
possibly damaging |
Het |
Klra4 |
A |
G |
6: 130,039,107 (GRCm39) |
I95T |
possibly damaging |
Het |
Krt84 |
A |
G |
15: 101,438,098 (GRCm39) |
F286L |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,350,260 (GRCm39) |
V704A |
probably benign |
Het |
Lypd6b |
A |
T |
2: 49,837,534 (GRCm39) |
S169C |
possibly damaging |
Het |
Mapk12 |
T |
C |
15: 89,024,611 (GRCm39) |
E22G |
probably benign |
Het |
Ncapg |
T |
C |
5: 45,833,983 (GRCm39) |
C340R |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,111,086 (GRCm39) |
L394P |
|
Het |
Nek1 |
T |
G |
8: 61,481,768 (GRCm39) |
S228A |
probably damaging |
Het |
Or2ak7 |
T |
C |
11: 58,574,722 (GRCm39) |
C8R |
probably benign |
Het |
Or2t29 |
A |
T |
11: 58,433,782 (GRCm39) |
C186* |
probably null |
Het |
Or2t44 |
T |
A |
11: 58,677,559 (GRCm39) |
F166L |
possibly damaging |
Het |
Or4c119 |
C |
T |
2: 88,986,719 (GRCm39) |
E267K |
possibly damaging |
Het |
Or56b1 |
C |
T |
7: 104,285,291 (GRCm39) |
R137C |
probably benign |
Het |
Pcdha8 |
C |
A |
18: 37,126,285 (GRCm39) |
P256T |
possibly damaging |
Het |
Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
Ptprn |
A |
T |
1: 75,229,018 (GRCm39) |
M799K |
probably damaging |
Het |
Rhpn2 |
A |
T |
7: 35,083,473 (GRCm39) |
|
probably benign |
Het |
Sae1 |
A |
G |
7: 16,070,668 (GRCm39) |
F281L |
probably benign |
Het |
Slc25a23 |
A |
G |
17: 57,354,309 (GRCm39) |
Y366H |
probably benign |
Het |
Slc25a25 |
G |
T |
2: 32,309,175 (GRCm39) |
T222K |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,659,452 (GRCm39) |
F914Y |
possibly damaging |
Het |
Spef2 |
C |
A |
15: 9,653,091 (GRCm39) |
V897L |
probably benign |
Het |
Spon2 |
C |
A |
5: 33,374,054 (GRCm39) |
E110* |
probably null |
Het |
Sstr2 |
A |
G |
11: 113,515,177 (GRCm39) |
N32S |
probably benign |
Het |
Stk4 |
T |
C |
2: 163,959,985 (GRCm39) |
V415A |
probably benign |
Het |
Tcaf1 |
T |
G |
6: 42,654,372 (GRCm39) |
T607P |
probably benign |
Het |
Ush1c |
C |
A |
7: 45,850,480 (GRCm39) |
L766F |
probably damaging |
Het |
Usp9y |
T |
C |
Y: 1,383,354 (GRCm39) |
I795V |
probably benign |
Het |
Vmn1r43 |
G |
A |
6: 89,846,877 (GRCm39) |
T203M |
probably damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,340,231 (GRCm39) |
S81P |
probably damaging |
Het |
Vps45 |
A |
G |
3: 95,960,345 (GRCm39) |
|
probably benign |
Het |
Xkr4 |
G |
A |
1: 3,286,358 (GRCm39) |
R611* |
probably null |
Het |
Zc3h6 |
T |
G |
2: 128,859,096 (GRCm39) |
Y1042* |
probably null |
Het |
Zfp236 |
A |
G |
18: 82,638,469 (GRCm39) |
S1384P |
possibly damaging |
Het |
Zfp800 |
A |
T |
6: 28,243,215 (GRCm39) |
N583K |
probably benign |
Het |
Zpld1 |
T |
C |
16: 55,061,764 (GRCm39) |
S206G |
probably benign |
Het |
Zxdc |
T |
A |
6: 90,349,821 (GRCm39) |
S372R |
probably damaging |
Het |
|
Other mutations in Wdr6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01548:Wdr6
|
APN |
9 |
108,452,096 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01757:Wdr6
|
APN |
9 |
108,453,427 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02096:Wdr6
|
APN |
9 |
108,453,752 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02577:Wdr6
|
APN |
9 |
108,453,140 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02625:Wdr6
|
APN |
9 |
108,452,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Wdr6
|
APN |
9 |
108,455,743 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03250:Wdr6
|
APN |
9 |
108,450,396 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4802001:Wdr6
|
UTSW |
9 |
108,451,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Wdr6
|
UTSW |
9 |
108,450,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Wdr6
|
UTSW |
9 |
108,452,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0378:Wdr6
|
UTSW |
9 |
108,453,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Wdr6
|
UTSW |
9 |
108,450,300 (GRCm39) |
missense |
probably benign |
0.41 |
R1620:Wdr6
|
UTSW |
9 |
108,451,854 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1753:Wdr6
|
UTSW |
9 |
108,452,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R1844:Wdr6
|
UTSW |
9 |
108,453,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Wdr6
|
UTSW |
9 |
108,450,378 (GRCm39) |
splice site |
probably null |
|
R1987:Wdr6
|
UTSW |
9 |
108,453,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Wdr6
|
UTSW |
9 |
108,452,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Wdr6
|
UTSW |
9 |
108,451,322 (GRCm39) |
missense |
probably benign |
0.00 |
R3900:Wdr6
|
UTSW |
9 |
108,452,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R4021:Wdr6
|
UTSW |
9 |
108,452,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4909:Wdr6
|
UTSW |
9 |
108,450,187 (GRCm39) |
missense |
probably benign |
0.28 |
R5073:Wdr6
|
UTSW |
9 |
108,451,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5748:Wdr6
|
UTSW |
9 |
108,452,981 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6039:Wdr6
|
UTSW |
9 |
108,450,994 (GRCm39) |
frame shift |
probably null |
|
R6039:Wdr6
|
UTSW |
9 |
108,450,994 (GRCm39) |
frame shift |
probably null |
|
R6254:Wdr6
|
UTSW |
9 |
108,452,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6724:Wdr6
|
UTSW |
9 |
108,452,093 (GRCm39) |
missense |
probably benign |
0.11 |
R7134:Wdr6
|
UTSW |
9 |
108,450,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Wdr6
|
UTSW |
9 |
108,453,238 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7296:Wdr6
|
UTSW |
9 |
108,451,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R7388:Wdr6
|
UTSW |
9 |
108,451,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R7443:Wdr6
|
UTSW |
9 |
108,451,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Wdr6
|
UTSW |
9 |
108,450,201 (GRCm39) |
missense |
probably benign |
0.14 |
R7672:Wdr6
|
UTSW |
9 |
108,450,947 (GRCm39) |
missense |
probably benign |
0.06 |
R7699:Wdr6
|
UTSW |
9 |
108,453,560 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7700:Wdr6
|
UTSW |
9 |
108,453,560 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8559:Wdr6
|
UTSW |
9 |
108,452,593 (GRCm39) |
missense |
probably benign |
0.34 |
R9273:Wdr6
|
UTSW |
9 |
108,450,691 (GRCm39) |
missense |
probably benign |
0.00 |
R9486:Wdr6
|
UTSW |
9 |
108,453,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Wdr6
|
UTSW |
9 |
108,453,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R9679:Wdr6
|
UTSW |
9 |
108,450,358 (GRCm39) |
missense |
probably benign |
0.27 |
|