Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg8 |
A |
G |
17: 84,999,916 (GRCm39) |
E189G |
possibly damaging |
Het |
Acad11 |
T |
C |
9: 103,968,931 (GRCm39) |
|
probably null |
Het |
Adcy7 |
G |
T |
8: 89,044,571 (GRCm39) |
R488L |
probably damaging |
Het |
Akt1 |
C |
T |
12: 112,625,714 (GRCm39) |
|
probably benign |
Het |
Ano9 |
C |
T |
7: 140,682,167 (GRCm39) |
|
probably benign |
Het |
Arhgap15 |
A |
G |
2: 43,953,820 (GRCm39) |
D182G |
possibly damaging |
Het |
Asxl3 |
T |
A |
18: 22,585,456 (GRCm39) |
V127D |
probably benign |
Het |
Cacna1g |
A |
G |
11: 94,319,955 (GRCm39) |
M1407T |
probably damaging |
Het |
Card9 |
A |
C |
2: 26,244,427 (GRCm39) |
|
probably benign |
Het |
Cdh5 |
A |
G |
8: 104,864,454 (GRCm39) |
N472D |
probably damaging |
Het |
Ceacam2 |
T |
A |
7: 25,227,379 (GRCm39) |
T343S |
probably benign |
Het |
Cic |
T |
A |
7: 24,990,282 (GRCm39) |
C1928S |
probably benign |
Het |
Clk3 |
C |
T |
9: 57,661,927 (GRCm39) |
W31* |
probably null |
Het |
Cntn4 |
A |
G |
6: 106,595,349 (GRCm39) |
T489A |
probably benign |
Het |
Crispld1 |
G |
A |
1: 17,826,529 (GRCm39) |
R431H |
probably damaging |
Het |
Crmp1 |
T |
A |
5: 37,436,199 (GRCm39) |
|
probably benign |
Het |
Cyld |
A |
G |
8: 89,456,218 (GRCm39) |
T423A |
possibly damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,736,198 (GRCm39) |
I84N |
probably damaging |
Het |
D2hgdh |
A |
G |
1: 93,757,507 (GRCm39) |
N141D |
probably damaging |
Het |
Dip2b |
T |
A |
15: 100,055,162 (GRCm39) |
L341Q |
probably damaging |
Het |
F3 |
C |
T |
3: 121,525,323 (GRCm39) |
T53I |
possibly damaging |
Het |
Fam227b |
T |
A |
2: 125,845,831 (GRCm39) |
Y386F |
probably benign |
Het |
Fmn1 |
A |
T |
2: 113,355,640 (GRCm39) |
T694S |
unknown |
Het |
Gcnt2 |
T |
A |
13: 41,040,856 (GRCm39) |
V5E |
probably benign |
Het |
Herpud1 |
G |
T |
8: 95,121,270 (GRCm39) |
E355* |
probably null |
Het |
Igf1r |
T |
C |
7: 67,843,144 (GRCm39) |
S752P |
probably benign |
Het |
Iqsec1 |
T |
C |
6: 90,649,057 (GRCm39) |
I687V |
possibly damaging |
Het |
Kdm5a |
T |
C |
6: 120,409,110 (GRCm39) |
S1598P |
probably damaging |
Het |
Klk1b9 |
A |
G |
7: 43,445,063 (GRCm39) |
E185G |
probably benign |
Het |
Myo16 |
G |
T |
8: 10,440,217 (GRCm39) |
R423L |
probably damaging |
Het |
Myo7b |
T |
C |
18: 32,100,207 (GRCm39) |
E1609G |
probably damaging |
Het |
Nom1 |
T |
A |
5: 29,644,814 (GRCm39) |
|
probably benign |
Het |
Nomo1 |
A |
G |
7: 45,727,480 (GRCm39) |
I1040V |
possibly damaging |
Het |
Or8b39 |
G |
A |
9: 37,996,741 (GRCm39) |
G203D |
probably damaging |
Het |
Paqr9 |
T |
C |
9: 95,442,748 (GRCm39) |
V246A |
probably benign |
Het |
Pfkfb4 |
A |
T |
9: 108,859,404 (GRCm39) |
D437V |
probably benign |
Het |
Phldb1 |
G |
T |
9: 44,622,223 (GRCm39) |
D797E |
probably benign |
Het |
Pkd1l3 |
A |
G |
8: 110,374,132 (GRCm39) |
E1399G |
probably damaging |
Het |
Plekhs1 |
G |
A |
19: 56,460,198 (GRCm39) |
C97Y |
probably damaging |
Het |
Plscr4 |
A |
T |
9: 92,372,044 (GRCm39) |
I272L |
possibly damaging |
Het |
Prlhr |
A |
C |
19: 60,456,366 (GRCm39) |
Y67D |
probably damaging |
Het |
Rab3gap2 |
A |
G |
1: 184,984,221 (GRCm39) |
|
probably benign |
Het |
Rad23b |
T |
C |
4: 55,382,511 (GRCm39) |
V238A |
probably benign |
Het |
Sel1l2 |
T |
C |
2: 140,117,380 (GRCm39) |
T164A |
possibly damaging |
Het |
Serpinh1 |
T |
A |
7: 98,996,199 (GRCm39) |
K295M |
probably damaging |
Het |
Slc45a4 |
T |
C |
15: 73,453,687 (GRCm39) |
E770G |
probably benign |
Het |
Spag4 |
T |
C |
2: 155,911,142 (GRCm39) |
L390P |
probably damaging |
Het |
Stip1 |
A |
G |
19: 7,012,857 (GRCm39) |
|
probably benign |
Het |
Tacr1 |
A |
G |
6: 82,380,739 (GRCm39) |
N50S |
probably damaging |
Het |
Tg |
T |
C |
15: 66,613,443 (GRCm39) |
V433A |
possibly damaging |
Het |
Usp40 |
A |
T |
1: 87,909,738 (GRCm39) |
I572K |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,917,308 (GRCm39) |
E3717D |
probably damaging |
Het |
Wdr81 |
T |
C |
11: 75,335,232 (GRCm39) |
N1778S |
probably benign |
Het |
Ylpm1 |
T |
A |
12: 85,095,965 (GRCm39) |
F1162Y |
probably damaging |
Het |
Zbtb10 |
T |
A |
3: 9,330,297 (GRCm39) |
F552I |
probably damaging |
Het |
Zfp507 |
T |
C |
7: 35,475,891 (GRCm39) |
I811V |
probably damaging |
Het |
Zfp663 |
A |
T |
2: 165,195,871 (GRCm39) |
V116D |
probably benign |
Het |
|
Other mutations in Ubap1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01681:Ubap1l
|
APN |
9 |
65,281,201 (GRCm39) |
missense |
probably benign |
0.00 |
R1437:Ubap1l
|
UTSW |
9 |
65,279,337 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1509:Ubap1l
|
UTSW |
9 |
65,279,237 (GRCm39) |
missense |
probably benign |
|
R1700:Ubap1l
|
UTSW |
9 |
65,279,025 (GRCm39) |
unclassified |
probably benign |
|
R1993:Ubap1l
|
UTSW |
9 |
65,279,078 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2106:Ubap1l
|
UTSW |
9 |
65,281,089 (GRCm39) |
missense |
probably benign |
0.00 |
R3963:Ubap1l
|
UTSW |
9 |
65,276,477 (GRCm39) |
start gained |
probably benign |
|
R5531:Ubap1l
|
UTSW |
9 |
65,278,973 (GRCm39) |
missense |
probably damaging |
0.96 |
R5699:Ubap1l
|
UTSW |
9 |
65,279,337 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5728:Ubap1l
|
UTSW |
9 |
65,276,570 (GRCm39) |
missense |
probably benign |
|
R5850:Ubap1l
|
UTSW |
9 |
65,281,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7384:Ubap1l
|
UTSW |
9 |
65,279,032 (GRCm39) |
unclassified |
probably benign |
|
R9148:Ubap1l
|
UTSW |
9 |
65,276,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R9174:Ubap1l
|
UTSW |
9 |
65,284,289 (GRCm39) |
missense |
probably benign |
0.00 |
|