Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
T |
A |
4: 144,344,598 (GRCm39) |
C125S |
probably benign |
Het |
Abcb8 |
T |
C |
5: 24,608,107 (GRCm39) |
L382P |
probably damaging |
Het |
Acot3 |
A |
G |
12: 84,105,724 (GRCm39) |
|
probably null |
Het |
Acsl6 |
A |
T |
11: 54,228,015 (GRCm39) |
Q345L |
probably benign |
Het |
Adcy8 |
A |
G |
15: 64,571,134 (GRCm39) |
S1170P |
probably damaging |
Het |
Ankrd28 |
T |
G |
14: 31,457,022 (GRCm39) |
D182A |
probably damaging |
Het |
B3galt5 |
A |
T |
16: 96,116,709 (GRCm39) |
H114L |
probably benign |
Het |
Bcas2 |
T |
A |
3: 103,085,740 (GRCm39) |
Y207* |
probably null |
Het |
Best1 |
A |
G |
19: 9,969,467 (GRCm39) |
L197P |
probably benign |
Het |
Chil6 |
C |
A |
3: 106,296,068 (GRCm39) |
C389F |
probably damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,253 (GRCm39) |
T168A |
probably damaging |
Het |
Ckmt1 |
C |
G |
2: 121,194,110 (GRCm39) |
|
probably benign |
Het |
Dhcr7 |
T |
C |
7: 143,401,160 (GRCm39) |
L441P |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,842,419 (GRCm39) |
M365V |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,010,764 (GRCm39) |
S974T |
probably damaging |
Het |
Dnajb13 |
T |
C |
7: 100,156,626 (GRCm39) |
D150G |
probably benign |
Het |
Eef2k |
C |
A |
7: 120,472,513 (GRCm39) |
|
probably benign |
Het |
Elp2 |
T |
A |
18: 24,748,267 (GRCm39) |
V213E |
probably damaging |
Het |
Fbxo43 |
A |
T |
15: 36,162,241 (GRCm39) |
|
probably null |
Het |
Gm11559 |
C |
A |
11: 99,755,412 (GRCm39) |
C20* |
probably null |
Het |
Gnb2 |
T |
C |
5: 137,527,454 (GRCm39) |
I213V |
probably benign |
Het |
Gnb5 |
C |
T |
9: 75,251,796 (GRCm39) |
T306I |
probably damaging |
Het |
Ica1 |
A |
T |
6: 8,667,257 (GRCm39) |
I303N |
possibly damaging |
Het |
Idh1 |
A |
G |
1: 65,204,295 (GRCm39) |
Y272H |
probably damaging |
Het |
Ikzf2 |
G |
A |
1: 69,578,256 (GRCm39) |
Q273* |
probably null |
Het |
Itpkb |
A |
T |
1: 180,154,790 (GRCm39) |
⇒1 |
probably benign |
Het |
Kntc1 |
C |
T |
5: 123,957,120 (GRCm39) |
T2143I |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Lmbrd1 |
C |
A |
1: 24,787,943 (GRCm39) |
D464E |
possibly damaging |
Het |
Med13 |
A |
G |
11: 86,169,757 (GRCm39) |
|
probably benign |
Het |
Mn1 |
T |
C |
5: 111,568,192 (GRCm39) |
F721L |
possibly damaging |
Het |
Myo9a |
T |
A |
9: 59,775,467 (GRCm39) |
L1026Q |
possibly damaging |
Het |
Or6c204 |
A |
T |
10: 129,022,718 (GRCm39) |
F191I |
probably benign |
Het |
P4htm |
A |
C |
9: 108,456,922 (GRCm39) |
D428E |
probably damaging |
Het |
Parp8 |
C |
T |
13: 117,013,116 (GRCm39) |
R602H |
probably damaging |
Het |
Pkd2 |
T |
A |
5: 104,646,372 (GRCm39) |
S726R |
probably damaging |
Het |
Pla2g6 |
A |
T |
15: 79,183,342 (GRCm39) |
I495N |
possibly damaging |
Het |
Psmd5 |
A |
G |
2: 34,746,500 (GRCm39) |
I359T |
probably benign |
Het |
Rassf6 |
T |
C |
5: 90,751,977 (GRCm39) |
H292R |
possibly damaging |
Het |
Rnf145 |
T |
C |
11: 44,450,915 (GRCm39) |
I413T |
probably damaging |
Het |
Rpn2 |
T |
A |
2: 157,125,516 (GRCm39) |
V9D |
possibly damaging |
Het |
Rpp30 |
T |
C |
19: 36,064,390 (GRCm39) |
L57P |
probably damaging |
Het |
Slc41a1 |
A |
G |
1: 131,774,325 (GRCm39) |
H464R |
possibly damaging |
Het |
Slc47a1 |
G |
T |
11: 61,260,087 (GRCm39) |
P163Q |
probably damaging |
Het |
Smc4 |
T |
A |
3: 68,915,443 (GRCm39) |
I165K |
probably damaging |
Het |
Stra6l |
T |
A |
4: 45,881,455 (GRCm39) |
I439K |
probably benign |
Het |
Syt9 |
C |
T |
7: 107,024,503 (GRCm39) |
T132I |
probably damaging |
Het |
Timd6 |
C |
T |
11: 46,465,433 (GRCm39) |
S9L |
unknown |
Het |
Trpm2 |
T |
C |
10: 77,774,187 (GRCm39) |
I471V |
possibly damaging |
Het |
Vmn1r91 |
A |
T |
7: 19,835,870 (GRCm39) |
H263L |
possibly damaging |
Het |
Zfp407 |
T |
C |
18: 84,579,169 (GRCm39) |
D648G |
probably benign |
Het |
Zpbp2 |
T |
C |
11: 98,445,584 (GRCm39) |
I150T |
probably damaging |
Het |
|
Other mutations in Uap1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01527:Uap1l1
|
APN |
2 |
25,253,816 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02437:Uap1l1
|
APN |
2 |
25,253,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Uap1l1
|
UTSW |
2 |
25,253,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Uap1l1
|
UTSW |
2 |
25,252,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Uap1l1
|
UTSW |
2 |
25,252,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R4808:Uap1l1
|
UTSW |
2 |
25,252,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Uap1l1
|
UTSW |
2 |
25,252,840 (GRCm39) |
missense |
probably damaging |
0.97 |
R5042:Uap1l1
|
UTSW |
2 |
25,252,097 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5560:Uap1l1
|
UTSW |
2 |
25,252,688 (GRCm39) |
missense |
probably benign |
|
R5634:Uap1l1
|
UTSW |
2 |
25,254,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Uap1l1
|
UTSW |
2 |
25,253,445 (GRCm39) |
intron |
probably benign |
|
R5973:Uap1l1
|
UTSW |
2 |
25,254,642 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6187:Uap1l1
|
UTSW |
2 |
25,252,741 (GRCm39) |
missense |
probably damaging |
0.98 |
R6966:Uap1l1
|
UTSW |
2 |
25,254,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Uap1l1
|
UTSW |
2 |
25,253,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R7356:Uap1l1
|
UTSW |
2 |
25,251,696 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8461:Uap1l1
|
UTSW |
2 |
25,255,422 (GRCm39) |
missense |
probably benign |
0.00 |
|