Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
G |
T |
16: 21,513,092 (GRCm39) |
L22M |
probably damaging |
Het |
Abca9 |
T |
C |
11: 109,998,384 (GRCm39) |
N1468S |
probably benign |
Het |
Abcc5 |
C |
T |
16: 20,163,446 (GRCm39) |
D1264N |
possibly damaging |
Het |
Abhd10 |
A |
G |
16: 45,553,099 (GRCm39) |
|
probably benign |
Het |
Acadvl |
G |
T |
11: 69,901,569 (GRCm39) |
A570E |
probably damaging |
Het |
Adgrb3 |
T |
A |
1: 25,586,629 (GRCm39) |
S355C |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,570,344 (GRCm39) |
V4953A |
possibly damaging |
Het |
Ano2 |
T |
A |
6: 125,992,536 (GRCm39) |
Y836* |
probably null |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Ccdc8 |
T |
A |
7: 16,730,537 (GRCm39) |
D675E |
possibly damaging |
Het |
Ccnb2 |
A |
G |
9: 70,326,170 (GRCm39) |
V58A |
probably benign |
Het |
Cdcp3 |
T |
A |
7: 130,879,295 (GRCm39) |
|
probably null |
Het |
Cdh24 |
A |
T |
14: 54,875,547 (GRCm39) |
Y296N |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,198,266 (GRCm39) |
E2054G |
unknown |
Het |
Cnot1 |
A |
T |
8: 96,454,276 (GRCm39) |
F2067I |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,813,334 (GRCm39) |
F329S |
|
Het |
Dact3 |
C |
A |
7: 16,619,840 (GRCm39) |
T445K |
unknown |
Het |
Dph6 |
C |
A |
2: 114,485,379 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
A |
1: 34,209,517 (GRCm39) |
C1195S |
probably damaging |
Het |
Eeig1 |
A |
G |
2: 32,456,346 (GRCm39) |
D336G |
possibly damaging |
Het |
Fat3 |
T |
A |
9: 15,899,620 (GRCm39) |
N3138Y |
probably damaging |
Het |
Fuca1 |
A |
G |
4: 135,660,405 (GRCm39) |
I308V |
probably benign |
Het |
Galnt5 |
A |
G |
2: 57,907,222 (GRCm39) |
R562G |
probably damaging |
Het |
Gas8 |
G |
T |
8: 124,249,718 (GRCm39) |
R44S |
probably damaging |
Het |
Gja5 |
T |
C |
3: 96,958,071 (GRCm39) |
S43P |
possibly damaging |
Het |
Gm14403 |
A |
G |
2: 177,200,405 (GRCm39) |
D117G |
probably benign |
Het |
Gmpr2 |
G |
A |
14: 55,910,491 (GRCm39) |
V58M |
probably damaging |
Het |
Gtpbp6 |
T |
A |
5: 110,252,950 (GRCm39) |
I301F |
probably damaging |
Het |
H2bc22 |
T |
A |
13: 21,971,762 (GRCm39) |
D26E |
probably benign |
Het |
Hdhd5 |
T |
C |
6: 120,498,212 (GRCm39) |
Y129C |
probably damaging |
Het |
Hemgn |
A |
G |
4: 46,396,504 (GRCm39) |
M244T |
probably benign |
Het |
Hoxa1 |
T |
G |
6: 52,135,238 (GRCm39) |
|
probably null |
Het |
Iglc1 |
T |
A |
16: 18,880,551 (GRCm39) |
H90L |
|
Het |
Lamb2 |
C |
T |
9: 108,366,423 (GRCm39) |
S1545F |
possibly damaging |
Het |
Mc4r |
T |
C |
18: 66,992,580 (GRCm39) |
T178A |
probably benign |
Het |
Mcam |
T |
A |
9: 44,050,955 (GRCm39) |
S346T |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,195,626 (GRCm39) |
S713P |
probably benign |
Het |
Mybl2 |
A |
G |
2: 162,914,752 (GRCm39) |
Y290C |
probably damaging |
Het |
Or4k44 |
T |
C |
2: 111,368,281 (GRCm39) |
M118V |
probably damaging |
Het |
Or7e168 |
A |
T |
9: 19,720,225 (GRCm39) |
I204F |
possibly damaging |
Het |
Pak6 |
A |
G |
2: 118,525,068 (GRCm39) |
T565A |
probably damaging |
Het |
Pde5a |
A |
G |
3: 122,568,250 (GRCm39) |
T284A |
probably benign |
Het |
Pkd1l2 |
A |
T |
8: 117,756,384 (GRCm39) |
F1616Y |
probably damaging |
Het |
Pp2d1 |
T |
C |
17: 53,822,907 (GRCm39) |
E53G |
probably benign |
Het |
Ppp3cc |
A |
C |
14: 70,478,394 (GRCm39) |
S269R |
probably benign |
Het |
Ptprb |
A |
C |
10: 116,205,214 (GRCm39) |
D1856A |
possibly damaging |
Het |
Rgs22 |
A |
T |
15: 36,040,856 (GRCm39) |
V1001E |
probably benign |
Het |
Rnf8 |
T |
A |
17: 29,847,980 (GRCm39) |
V344E |
probably benign |
Het |
Rpn1 |
T |
C |
6: 88,061,550 (GRCm39) |
L13P |
possibly damaging |
Het |
Rsbn1 |
A |
T |
3: 103,822,326 (GRCm39) |
H187L |
probably benign |
Het |
Sdr16c6 |
T |
A |
4: 4,058,801 (GRCm39) |
I262F |
not run |
Het |
Sec22a |
A |
G |
16: 35,149,894 (GRCm39) |
F211L |
probably benign |
Het |
Slc16a4 |
G |
A |
3: 107,205,297 (GRCm39) |
A42T |
possibly damaging |
Het |
Smap1 |
T |
A |
1: 23,887,376 (GRCm39) |
Q386L |
probably benign |
Het |
Sos1 |
A |
T |
17: 80,787,323 (GRCm39) |
F10L |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,776,196 (GRCm39) |
T202A |
probably damaging |
Het |
Stab1 |
C |
A |
14: 30,862,578 (GRCm39) |
V2282L |
probably benign |
Het |
Tex55 |
C |
T |
16: 38,648,453 (GRCm39) |
D219N |
possibly damaging |
Het |
Tmprss11f |
C |
T |
5: 86,672,019 (GRCm39) |
G391D |
probably damaging |
Het |
Tnfaip2 |
A |
G |
12: 111,412,072 (GRCm39) |
S158G |
probably damaging |
Het |
Trav6d-5 |
A |
G |
14: 53,032,843 (GRCm39) |
T31A |
probably benign |
Het |
Tst |
G |
A |
15: 78,289,903 (GRCm39) |
A44V |
probably damaging |
Het |
Vmn1r210 |
A |
T |
13: 23,011,405 (GRCm39) |
F294I |
probably benign |
Het |
Vwc2 |
T |
C |
11: 11,066,415 (GRCm39) |
F168L |
probably damaging |
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Zfp605 |
A |
G |
5: 110,275,386 (GRCm39) |
Y168C |
probably benign |
Het |
Zfp790 |
T |
A |
7: 29,525,130 (GRCm39) |
Y49* |
probably null |
Het |
Zfp93 |
T |
C |
7: 23,975,794 (GRCm39) |
F593S |
probably damaging |
Het |
Zfr |
C |
T |
15: 12,160,614 (GRCm39) |
T729I |
possibly damaging |
Het |
|
Other mutations in Fbxw25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03330:Fbxw25
|
APN |
9 |
109,474,307 (GRCm39) |
missense |
probably benign |
0.00 |
doughnuts
|
UTSW |
9 |
109,479,132 (GRCm39) |
missense |
|
|
goodtimes
|
UTSW |
9 |
109,492,442 (GRCm39) |
critical splice donor site |
probably null |
|
shakeys
|
UTSW |
9 |
109,483,651 (GRCm39) |
missense |
|
|
R0158:Fbxw25
|
UTSW |
9 |
109,483,720 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0850:Fbxw25
|
UTSW |
9 |
109,478,685 (GRCm39) |
missense |
probably benign |
|
R1109:Fbxw25
|
UTSW |
9 |
109,479,128 (GRCm39) |
missense |
probably benign |
0.00 |
R1386:Fbxw25
|
UTSW |
9 |
109,483,709 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1609:Fbxw25
|
UTSW |
9 |
109,492,578 (GRCm39) |
missense |
probably benign |
0.11 |
R1750:Fbxw25
|
UTSW |
9 |
109,479,141 (GRCm39) |
missense |
probably benign |
0.23 |
R1977:Fbxw25
|
UTSW |
9 |
109,481,924 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2427:Fbxw25
|
UTSW |
9 |
109,481,928 (GRCm39) |
missense |
probably benign |
0.09 |
R3841:Fbxw25
|
UTSW |
9 |
109,491,202 (GRCm39) |
nonsense |
probably null |
|
R4356:Fbxw25
|
UTSW |
9 |
109,491,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Fbxw25
|
UTSW |
9 |
109,480,705 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5024:Fbxw25
|
UTSW |
9 |
109,492,442 (GRCm39) |
critical splice donor site |
probably null |
|
R5175:Fbxw25
|
UTSW |
9 |
109,493,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Fbxw25
|
UTSW |
9 |
109,492,573 (GRCm39) |
missense |
probably benign |
0.04 |
R5389:Fbxw25
|
UTSW |
9 |
109,481,954 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5493:Fbxw25
|
UTSW |
9 |
109,481,984 (GRCm39) |
missense |
probably benign |
0.01 |
R6268:Fbxw25
|
UTSW |
9 |
109,483,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Fbxw25
|
UTSW |
9 |
109,480,699 (GRCm39) |
missense |
probably benign |
0.29 |
R7275:Fbxw25
|
UTSW |
9 |
109,483,660 (GRCm39) |
missense |
|
|
R7492:Fbxw25
|
UTSW |
9 |
109,493,598 (GRCm39) |
critical splice donor site |
probably null |
|
R7784:Fbxw25
|
UTSW |
9 |
109,479,187 (GRCm39) |
missense |
|
|
R7861:Fbxw25
|
UTSW |
9 |
109,493,625 (GRCm39) |
nonsense |
probably null |
|
R7887:Fbxw25
|
UTSW |
9 |
109,478,662 (GRCm39) |
critical splice donor site |
probably null |
|
R8973:Fbxw25
|
UTSW |
9 |
109,479,132 (GRCm39) |
missense |
|
|
R9517:Fbxw25
|
UTSW |
9 |
109,480,892 (GRCm39) |
missense |
|
|
R9563:Fbxw25
|
UTSW |
9 |
109,483,676 (GRCm39) |
missense |
|
|
R9565:Fbxw25
|
UTSW |
9 |
109,483,676 (GRCm39) |
missense |
|
|
X0023:Fbxw25
|
UTSW |
9 |
109,480,843 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Fbxw25
|
UTSW |
9 |
109,480,806 (GRCm39) |
missense |
|
|
|