Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr6 |
C |
T |
10: 89,550,841 (GRCm39) |
V318I |
probably benign |
Het |
Adam29 |
A |
G |
8: 56,325,659 (GRCm39) |
I265T |
probably benign |
Het |
Ankdd1a |
A |
T |
9: 65,415,422 (GRCm39) |
|
probably benign |
Het |
Arcn1 |
T |
C |
9: 44,655,259 (GRCm39) |
T501A |
possibly damaging |
Het |
B3gntl1 |
A |
T |
11: 121,521,690 (GRCm39) |
F166I |
possibly damaging |
Het |
Brap |
T |
C |
5: 121,822,524 (GRCm39) |
S467P |
possibly damaging |
Het |
Cenpb |
A |
G |
2: 131,020,322 (GRCm39) |
V492A |
unknown |
Het |
Ces1b |
C |
A |
8: 93,786,948 (GRCm39) |
G477V |
probably damaging |
Het |
Ces1b |
C |
T |
8: 93,786,949 (GRCm39) |
G477R |
probably damaging |
Het |
Cfap65 |
T |
C |
1: 74,942,382 (GRCm39) |
K1724R |
probably benign |
Het |
Chrd |
A |
T |
16: 20,553,270 (GRCm39) |
Q182L |
probably benign |
Het |
Chrnb2 |
T |
C |
3: 89,664,457 (GRCm39) |
T486A |
probably benign |
Het |
Col25a1 |
A |
T |
3: 130,354,466 (GRCm39) |
|
probably null |
Het |
Col4a1 |
A |
G |
8: 11,295,916 (GRCm39) |
Y101H |
unknown |
Het |
Crybg1 |
T |
C |
10: 43,879,428 (GRCm39) |
T587A |
probably damaging |
Het |
Ctnnal1 |
T |
A |
4: 56,835,374 (GRCm39) |
N301I |
possibly damaging |
Het |
Cyp2f2 |
A |
T |
7: 26,831,995 (GRCm39) |
N417Y |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,009,546 (GRCm39) |
E3800D |
possibly damaging |
Het |
Dync2i1 |
A |
G |
12: 116,193,234 (GRCm39) |
S573P |
probably damaging |
Het |
Ehmt2 |
C |
A |
17: 35,127,489 (GRCm39) |
T906K |
probably damaging |
Het |
Fbxo15 |
A |
G |
18: 84,978,200 (GRCm39) |
H183R |
possibly damaging |
Het |
Fgl1 |
T |
A |
8: 41,650,368 (GRCm39) |
K194* |
probably null |
Het |
Fxr1 |
G |
A |
3: 34,108,430 (GRCm39) |
V314I |
possibly damaging |
Het |
Hrnr |
A |
G |
3: 93,239,443 (GRCm39) |
Q3227R |
unknown |
Het |
Ier5 |
G |
A |
1: 154,974,716 (GRCm39) |
A154V |
probably benign |
Het |
Igkc |
T |
G |
6: 70,703,502 (GRCm39) |
L28V |
|
Het |
Kcnh1 |
G |
A |
1: 191,903,722 (GRCm39) |
G54D |
probably damaging |
Het |
Kcnn1 |
C |
T |
8: 71,305,297 (GRCm39) |
|
probably null |
Het |
Kifbp |
C |
T |
10: 62,395,491 (GRCm39) |
D384N |
possibly damaging |
Het |
Klra2 |
T |
A |
6: 131,197,198 (GRCm39) |
N234I |
possibly damaging |
Het |
Krtap4-9 |
T |
C |
11: 99,676,454 (GRCm39) |
I125T |
unknown |
Het |
Lrig2 |
T |
C |
3: 104,368,993 (GRCm39) |
T897A |
probably benign |
Het |
Lyve1 |
G |
T |
7: 110,452,999 (GRCm39) |
T199K |
probably damaging |
Het |
Myorg |
T |
C |
4: 41,498,812 (GRCm39) |
T273A |
probably benign |
Het |
Napa |
A |
G |
7: 15,846,551 (GRCm39) |
D113G |
possibly damaging |
Het |
Neurog1 |
GGTG |
GGTGTG |
13: 56,399,098 (GRCm39) |
|
probably null |
Het |
Nf1 |
T |
A |
11: 79,437,964 (GRCm39) |
H91Q |
probably damaging |
Het |
Or4c11c |
T |
C |
2: 88,662,256 (GRCm39) |
M265T |
probably benign |
Het |
Or4n4 |
A |
G |
14: 50,519,236 (GRCm39) |
I158T |
probably benign |
Het |
Or52e3 |
A |
T |
7: 102,869,446 (GRCm39) |
N174Y |
probably benign |
Het |
Or5k16 |
T |
A |
16: 58,736,248 (GRCm39) |
Y252F |
probably damaging |
Het |
Or7g16 |
A |
G |
9: 18,726,919 (GRCm39) |
S224P |
probably damaging |
Het |
Pccb |
A |
T |
9: 100,867,220 (GRCm39) |
Y455* |
probably null |
Het |
Pdk2 |
A |
T |
11: 94,923,339 (GRCm39) |
I95N |
probably damaging |
Het |
Pik3c2g |
G |
A |
6: 139,714,436 (GRCm39) |
R196H |
|
Het |
Pkd1l2 |
A |
G |
8: 117,726,660 (GRCm39) |
L2282P |
probably damaging |
Het |
Plppr2 |
TCGCC |
TC |
9: 21,855,727 (GRCm39) |
|
probably benign |
Het |
Prdm1 |
A |
T |
10: 44,315,749 (GRCm39) |
S796T |
probably benign |
Het |
Rb1 |
A |
G |
14: 73,503,000 (GRCm39) |
F424L |
probably damaging |
Het |
Retreg3 |
A |
G |
11: 100,992,852 (GRCm39) |
L190P |
probably damaging |
Het |
Rffl |
A |
G |
11: 82,700,864 (GRCm39) |
Y321H |
probably damaging |
Het |
Rlbp1 |
A |
G |
7: 79,025,704 (GRCm39) |
Y246H |
probably damaging |
Het |
Rock2 |
T |
A |
12: 17,015,655 (GRCm39) |
|
probably benign |
Het |
Slc17a3 |
C |
A |
13: 24,039,575 (GRCm39) |
C244* |
probably null |
Het |
Snapc1 |
T |
C |
12: 74,021,812 (GRCm39) |
S304P |
probably benign |
Het |
Sp9 |
T |
C |
2: 73,104,019 (GRCm39) |
L191P |
probably damaging |
Het |
Spag17 |
A |
T |
3: 99,889,738 (GRCm39) |
E202D |
probably benign |
Het |
Ss18 |
A |
G |
18: 14,760,344 (GRCm39) |
*419R |
probably null |
Het |
Tacc2 |
A |
G |
7: 130,276,421 (GRCm39) |
E1824G |
possibly damaging |
Het |
Tacc3 |
T |
A |
5: 33,824,029 (GRCm39) |
|
probably benign |
Het |
Tfap2a |
A |
T |
13: 40,870,829 (GRCm39) |
L353Q |
probably damaging |
Het |
Ugt3a1 |
A |
G |
15: 9,367,345 (GRCm39) |
I363V |
possibly damaging |
Het |
Vmn1r158 |
A |
G |
7: 22,489,775 (GRCm39) |
C145R |
probably damaging |
Het |
Vmn1r23 |
A |
T |
6: 57,903,352 (GRCm39) |
I142K |
probably damaging |
Het |
Vmn2r15 |
A |
T |
5: 109,434,874 (GRCm39) |
I610N |
probably benign |
Het |
Zbtb7c |
T |
C |
18: 76,270,190 (GRCm39) |
Y93H |
probably damaging |
Het |
Zfp62 |
A |
G |
11: 49,107,238 (GRCm39) |
N443S |
probably damaging |
Het |
|
Other mutations in Yy1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Yy1
|
APN |
12 |
108,781,463 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02158:Yy1
|
APN |
12 |
108,780,525 (GRCm39) |
splice site |
probably benign |
|
IGL02223:Yy1
|
APN |
12 |
108,759,466 (GRCm39) |
missense |
unknown |
|
IGL02412:Yy1
|
APN |
12 |
108,760,023 (GRCm39) |
splice site |
probably benign |
|
IGL02718:Yy1
|
APN |
12 |
108,781,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Yy1
|
UTSW |
12 |
108,759,457 (GRCm39) |
missense |
unknown |
|
R1341:Yy1
|
UTSW |
12 |
108,759,445 (GRCm39) |
missense |
unknown |
|
R1855:Yy1
|
UTSW |
12 |
108,759,916 (GRCm39) |
small insertion |
probably benign |
|
R1989:Yy1
|
UTSW |
12 |
108,772,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Yy1
|
UTSW |
12 |
108,759,916 (GRCm39) |
small insertion |
probably benign |
|
R4566:Yy1
|
UTSW |
12 |
108,778,889 (GRCm39) |
missense |
probably damaging |
0.98 |
R4717:Yy1
|
UTSW |
12 |
108,759,972 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5041:Yy1
|
UTSW |
12 |
108,759,557 (GRCm39) |
small insertion |
probably benign |
|
R5089:Yy1
|
UTSW |
12 |
108,759,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5597:Yy1
|
UTSW |
12 |
108,781,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5907:Yy1
|
UTSW |
12 |
108,772,354 (GRCm39) |
intron |
probably benign |
|
R6876:Yy1
|
UTSW |
12 |
108,772,518 (GRCm39) |
missense |
probably benign |
0.13 |
R6878:Yy1
|
UTSW |
12 |
108,780,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Yy1
|
UTSW |
12 |
108,759,594 (GRCm39) |
missense |
probably benign |
0.28 |
R8218:Yy1
|
UTSW |
12 |
108,759,619 (GRCm39) |
missense |
probably benign |
0.00 |
R8378:Yy1
|
UTSW |
12 |
108,759,562 (GRCm39) |
missense |
unknown |
|
R8808:Yy1
|
UTSW |
12 |
108,759,506 (GRCm39) |
small deletion |
probably benign |
|
R9072:Yy1
|
UTSW |
12 |
108,759,921 (GRCm39) |
missense |
probably benign |
0.19 |
R9073:Yy1
|
UTSW |
12 |
108,759,921 (GRCm39) |
missense |
probably benign |
0.19 |
R9672:Yy1
|
UTSW |
12 |
108,759,584 (GRCm39) |
missense |
unknown |
|
R9749:Yy1
|
UTSW |
12 |
108,772,417 (GRCm39) |
missense |
possibly damaging |
0.95 |
|