Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
A |
16: 14,265,354 (GRCm39) |
S769T |
probably damaging |
Het |
Apoe |
G |
A |
7: 19,431,461 (GRCm39) |
T52M |
probably damaging |
Het |
Arhgef10l |
A |
C |
4: 140,314,126 (GRCm39) |
M230R |
probably benign |
Het |
Cdkl4 |
A |
T |
17: 80,832,781 (GRCm39) |
I321N |
probably benign |
Het |
Ceacam5 |
T |
C |
7: 17,481,391 (GRCm39) |
|
probably null |
Het |
Cfap70 |
T |
C |
14: 20,451,107 (GRCm39) |
|
probably null |
Het |
Clasp2 |
A |
G |
9: 113,602,785 (GRCm39) |
Y195C |
probably damaging |
Het |
Clip2 |
T |
C |
5: 134,520,779 (GRCm39) |
I999V |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,112,138 (GRCm39) |
D476G |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,666,152 (GRCm39) |
M1I |
probably null |
Het |
Cyp27a1 |
T |
C |
1: 74,775,047 (GRCm39) |
V292A |
possibly damaging |
Het |
Cyp2c29 |
A |
G |
19: 39,317,669 (GRCm39) |
Y385C |
probably damaging |
Het |
Dsg3 |
A |
C |
18: 20,666,583 (GRCm39) |
R597S |
probably benign |
Het |
Fam131c |
T |
C |
4: 141,109,653 (GRCm39) |
I95T |
probably damaging |
Het |
Fam13b |
A |
T |
18: 34,606,684 (GRCm39) |
C302* |
probably null |
Het |
Fkbp15 |
T |
C |
4: 62,226,315 (GRCm39) |
K745E |
possibly damaging |
Het |
Flg |
T |
A |
3: 93,188,688 (GRCm39) |
|
probably benign |
Het |
Gm11559 |
T |
C |
11: 99,755,542 (GRCm39) |
C64R |
unknown |
Het |
Helt |
T |
C |
8: 46,745,571 (GRCm39) |
D104G |
probably damaging |
Het |
Helz2 |
T |
C |
2: 180,876,862 (GRCm39) |
T1211A |
probably benign |
Het |
Ifna9 |
T |
C |
4: 88,510,487 (GRCm39) |
R46G |
possibly damaging |
Het |
Kif20b |
G |
A |
19: 34,911,841 (GRCm39) |
V235I |
probably benign |
Het |
Kif7 |
A |
G |
7: 79,363,842 (GRCm39) |
V22A |
possibly damaging |
Het |
Klra9 |
G |
T |
6: 130,155,995 (GRCm39) |
Y253* |
probably null |
Het |
Lipf |
A |
T |
19: 33,950,944 (GRCm39) |
Y305F |
probably benign |
Het |
Lpar1 |
A |
G |
4: 58,486,875 (GRCm39) |
L132P |
possibly damaging |
Het |
Magi1 |
A |
T |
6: 93,676,770 (GRCm39) |
V834E |
probably damaging |
Het |
Meltf |
T |
C |
16: 31,709,594 (GRCm39) |
Y432H |
probably benign |
Het |
Mroh2a |
G |
C |
1: 88,185,524 (GRCm39) |
E1510D |
probably damaging |
Het |
Myo1f |
T |
C |
17: 33,795,621 (GRCm39) |
L59P |
probably damaging |
Het |
Naa25 |
G |
A |
5: 121,556,024 (GRCm39) |
D271N |
probably damaging |
Het |
Or10ag55-ps1 |
A |
T |
2: 87,139,951 (GRCm39) |
I273F |
probably damaging |
Het |
Or8u3-ps |
A |
T |
2: 85,952,752 (GRCm39) |
I162F |
possibly damaging |
Het |
Otoa |
A |
G |
7: 120,701,828 (GRCm39) |
Q169R |
probably damaging |
Het |
Pde4dip |
C |
T |
3: 97,617,660 (GRCm39) |
D1723N |
probably damaging |
Het |
Ptdss2 |
T |
C |
7: 140,732,124 (GRCm39) |
V175A |
probably damaging |
Het |
Rdh8 |
G |
T |
9: 20,734,696 (GRCm39) |
R121L |
probably damaging |
Het |
Rpl23 |
T |
C |
11: 97,669,111 (GRCm39) |
|
probably null |
Het |
Scn5a |
T |
C |
9: 119,363,646 (GRCm39) |
D498G |
probably damaging |
Het |
Slc39a14 |
G |
C |
14: 70,544,177 (GRCm39) |
L470V |
probably damaging |
Het |
Smok2a |
C |
T |
17: 13,445,317 (GRCm39) |
A298V |
probably damaging |
Het |
Tesk2 |
A |
C |
4: 116,660,046 (GRCm39) |
D388A |
probably damaging |
Het |
Tnik |
G |
A |
3: 28,666,119 (GRCm39) |
|
probably null |
Het |
Ube3a |
T |
A |
7: 58,925,931 (GRCm39) |
Y236* |
probably null |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Vinac1 |
T |
C |
2: 128,881,465 (GRCm39) |
T154A |
possibly damaging |
Het |
Vmn1r74 |
A |
T |
7: 11,581,131 (GRCm39) |
I144L |
possibly damaging |
Het |
Vmn2r1 |
G |
A |
3: 64,008,766 (GRCm39) |
D482N |
probably benign |
Het |
Vwf |
T |
C |
6: 125,616,363 (GRCm39) |
|
probably null |
Het |
Zfp703 |
C |
G |
8: 27,469,355 (GRCm39) |
P340A |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,888,842 (GRCm39) |
S789G |
probably benign |
Het |
|
Other mutations in Wdr97 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6006:Wdr97
|
UTSW |
15 |
76,241,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Wdr97
|
UTSW |
15 |
76,239,895 (GRCm39) |
nonsense |
probably null |
|
R6544:Wdr97
|
UTSW |
15 |
76,242,478 (GRCm39) |
missense |
probably benign |
0.00 |
R6545:Wdr97
|
UTSW |
15 |
76,247,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Wdr97
|
UTSW |
15 |
76,239,178 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6803:Wdr97
|
UTSW |
15 |
76,240,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Wdr97
|
UTSW |
15 |
76,241,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Wdr97
|
UTSW |
15 |
76,241,949 (GRCm39) |
nonsense |
probably null |
|
R7793:Wdr97
|
UTSW |
15 |
76,243,307 (GRCm39) |
missense |
|
|
R7985:Wdr97
|
UTSW |
15 |
76,245,687 (GRCm39) |
missense |
|
|
R8008:Wdr97
|
UTSW |
15 |
76,244,832 (GRCm39) |
missense |
|
|
R8170:Wdr97
|
UTSW |
15 |
76,247,819 (GRCm39) |
missense |
|
|
R8171:Wdr97
|
UTSW |
15 |
76,247,819 (GRCm39) |
missense |
|
|
R8267:Wdr97
|
UTSW |
15 |
76,240,794 (GRCm39) |
missense |
|
|
R8337:Wdr97
|
UTSW |
15 |
76,245,684 (GRCm39) |
missense |
|
|
R8478:Wdr97
|
UTSW |
15 |
76,247,629 (GRCm39) |
splice site |
probably null |
|
R8735:Wdr97
|
UTSW |
15 |
76,240,775 (GRCm39) |
missense |
|
|
R8958:Wdr97
|
UTSW |
15 |
76,245,694 (GRCm39) |
missense |
|
|
R9385:Wdr97
|
UTSW |
15 |
76,240,367 (GRCm39) |
missense |
|
|
R9440:Wdr97
|
UTSW |
15 |
76,245,064 (GRCm39) |
missense |
|
|
R9657:Wdr97
|
UTSW |
15 |
76,245,476 (GRCm39) |
missense |
|
|
R9672:Wdr97
|
UTSW |
15 |
76,240,377 (GRCm39) |
missense |
|
|
R9778:Wdr97
|
UTSW |
15 |
76,241,125 (GRCm39) |
missense |
|
|
RF004:Wdr97
|
UTSW |
15 |
76,247,373 (GRCm39) |
frame shift |
probably null |
|
RF009:Wdr97
|
UTSW |
15 |
76,247,367 (GRCm39) |
frame shift |
probably null |
|
RF016:Wdr97
|
UTSW |
15 |
76,240,172 (GRCm39) |
missense |
|
|
RF030:Wdr97
|
UTSW |
15 |
76,247,365 (GRCm39) |
frame shift |
probably null |
|
Z1177:Wdr97
|
UTSW |
15 |
76,247,330 (GRCm39) |
missense |
|
|
Z1177:Wdr97
|
UTSW |
15 |
76,239,130 (GRCm39) |
missense |
|
|
|