Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acta2 |
C |
T |
19: 34,220,839 (GRCm39) |
D290N |
probably damaging |
Het |
Adam18 |
T |
C |
8: 25,101,116 (GRCm39) |
D682G |
probably benign |
Het |
Ankrd46 |
A |
G |
15: 36,485,989 (GRCm39) |
V88A |
possibly damaging |
Het |
Ankub1 |
T |
A |
3: 57,572,807 (GRCm39) |
K305I |
probably damaging |
Het |
Atrn |
T |
A |
2: 130,812,147 (GRCm39) |
|
probably null |
Het |
Bambi |
A |
T |
18: 3,511,406 (GRCm39) |
T76S |
probably benign |
Het |
Cacna1a |
T |
A |
8: 85,310,283 (GRCm39) |
V1447E |
probably damaging |
Het |
Calcoco2 |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
11: 95,990,808 (GRCm39) |
|
probably benign |
Het |
Clcn2 |
A |
G |
16: 20,527,210 (GRCm39) |
M629T |
probably damaging |
Het |
Clcn4 |
T |
C |
7: 7,290,780 (GRCm39) |
N673S |
probably benign |
Het |
Col20a1 |
T |
C |
2: 180,628,371 (GRCm39) |
F15S |
probably benign |
Het |
Col2a1 |
G |
A |
15: 97,898,458 (GRCm39) |
Q39* |
probably null |
Het |
Creb3 |
A |
G |
4: 43,563,332 (GRCm39) |
E119G |
probably benign |
Het |
Dnah5 |
A |
C |
15: 28,245,830 (GRCm39) |
D556A |
probably damaging |
Het |
Edar |
C |
T |
10: 58,446,348 (GRCm39) |
M192I |
possibly damaging |
Het |
Fam91a1 |
A |
G |
15: 58,320,209 (GRCm39) |
M634V |
probably benign |
Het |
Fbxo10 |
C |
T |
4: 45,051,699 (GRCm39) |
V471I |
not run |
Het |
Fer1l5 |
T |
C |
1: 36,460,967 (GRCm39) |
F2032L |
probably benign |
Het |
Gm5150 |
A |
C |
3: 16,060,485 (GRCm39) |
M1R |
probably null |
Het |
Grin1 |
T |
C |
2: 25,188,202 (GRCm39) |
E509G |
probably benign |
Het |
Igkv10-94 |
C |
T |
6: 68,681,913 (GRCm39) |
|
probably benign |
Het |
Il18bp |
A |
G |
7: 101,666,002 (GRCm39) |
Y59H |
possibly damaging |
Het |
Ints8 |
A |
T |
4: 11,254,062 (GRCm39) |
C17S |
probably benign |
Het |
Kcnmb1 |
T |
C |
11: 33,916,275 (GRCm39) |
Y74H |
probably damaging |
Het |
Kpna1 |
T |
C |
16: 35,843,565 (GRCm39) |
V313A |
probably benign |
Het |
Lrp4 |
C |
T |
2: 91,321,061 (GRCm39) |
T1029I |
possibly damaging |
Het |
Lrrc7 |
A |
T |
3: 158,059,099 (GRCm39) |
C3S |
probably damaging |
Het |
Lyst |
C |
A |
13: 13,810,450 (GRCm39) |
H707N |
probably benign |
Het |
Map3k20 |
A |
G |
2: 72,202,098 (GRCm39) |
K148R |
probably damaging |
Het |
Mcidas |
G |
A |
13: 113,135,521 (GRCm39) |
G315S |
probably damaging |
Het |
Miip |
C |
T |
4: 147,947,375 (GRCm39) |
G236S |
probably benign |
Het |
Mocs1 |
T |
A |
17: 49,746,561 (GRCm39) |
I177N |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,399,850 (GRCm39) |
D441G |
unknown |
Het |
Ncoa1 |
T |
C |
12: 4,328,186 (GRCm39) |
N884S |
probably benign |
Het |
Or12j4 |
A |
G |
7: 140,046,696 (GRCm39) |
N194S |
probably damaging |
Het |
Or51a39 |
A |
G |
7: 102,363,389 (GRCm39) |
V77A |
probably benign |
Het |
Padi6 |
A |
T |
4: 140,455,073 (GRCm39) |
F621L |
probably damaging |
Het |
Pde8b |
C |
A |
13: 95,223,347 (GRCm39) |
M197I |
possibly damaging |
Het |
Pear1 |
T |
A |
3: 87,659,522 (GRCm39) |
I771L |
probably benign |
Het |
Poli |
A |
G |
18: 70,655,891 (GRCm39) |
L281P |
probably damaging |
Het |
Prdm12 |
T |
C |
2: 31,530,231 (GRCm39) |
W41R |
probably damaging |
Het |
Prkdc |
T |
G |
16: 15,532,870 (GRCm39) |
S1500A |
probably benign |
Het |
Prune2 |
T |
A |
19: 17,096,798 (GRCm39) |
H767Q |
probably benign |
Het |
Rasgef1b |
G |
A |
5: 99,382,403 (GRCm39) |
Q196* |
probably null |
Het |
Rnpc3 |
A |
T |
3: 113,416,096 (GRCm39) |
L121* |
probably null |
Het |
Rpp14 |
A |
G |
14: 8,083,724 (GRCm38) |
M1V |
probably null |
Het |
Ryr2 |
T |
A |
13: 11,610,610 (GRCm39) |
D4072V |
probably damaging |
Het |
Sgms1 |
T |
C |
19: 32,102,765 (GRCm39) |
H314R |
probably damaging |
Het |
Slc37a3 |
A |
T |
6: 39,324,244 (GRCm39) |
Y335N |
probably damaging |
Het |
Tcp11l1 |
A |
T |
2: 104,536,837 (GRCm39) |
H9Q |
probably benign |
Het |
Tnrc6a |
T |
A |
7: 122,779,057 (GRCm39) |
M1256K |
probably damaging |
Het |
Trpc6 |
A |
G |
9: 8,609,910 (GRCm39) |
N126S |
probably damaging |
Het |
Tut4 |
T |
G |
4: 108,374,715 (GRCm39) |
C933G |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,120,373 (GRCm39) |
F266S |
possibly damaging |
Het |
Uimc1 |
A |
G |
13: 55,217,550 (GRCm39) |
V424A |
possibly damaging |
Het |
Utrn |
T |
C |
10: 12,573,873 (GRCm39) |
I1066V |
probably benign |
Het |
Vmn1r204 |
A |
G |
13: 22,740,404 (GRCm39) |
T12A |
probably benign |
Het |
Vmn1r57 |
T |
A |
7: 5,223,613 (GRCm39) |
I46N |
possibly damaging |
Het |
Vmn1r91 |
T |
C |
7: 19,835,839 (GRCm39) |
Y253H |
probably benign |
Het |
Vmn2r14 |
T |
A |
5: 109,369,219 (GRCm39) |
H118L |
probably benign |
Het |
Zfp775 |
A |
G |
6: 48,597,404 (GRCm39) |
K426R |
probably benign |
Het |
|
Other mutations in Six4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01635:Six4
|
APN |
12 |
73,155,971 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02045:Six4
|
APN |
12 |
73,155,429 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02678:Six4
|
APN |
12 |
73,159,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2473:Six4
|
UTSW |
12 |
73,150,949 (GRCm39) |
missense |
probably benign |
0.00 |
R3409:Six4
|
UTSW |
12 |
73,159,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R3410:Six4
|
UTSW |
12 |
73,159,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R3411:Six4
|
UTSW |
12 |
73,159,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R4175:Six4
|
UTSW |
12 |
73,155,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Six4
|
UTSW |
12 |
73,155,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Six4
|
UTSW |
12 |
73,150,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4303:Six4
|
UTSW |
12 |
73,159,314 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5013:Six4
|
UTSW |
12 |
73,150,400 (GRCm39) |
missense |
probably benign |
0.37 |
R5782:Six4
|
UTSW |
12 |
73,150,832 (GRCm39) |
missense |
probably benign |
0.02 |
R5794:Six4
|
UTSW |
12 |
73,159,124 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6429:Six4
|
UTSW |
12 |
73,150,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R6650:Six4
|
UTSW |
12 |
73,150,299 (GRCm39) |
missense |
probably benign |
0.04 |
R7018:Six4
|
UTSW |
12 |
73,155,727 (GRCm39) |
missense |
probably benign |
0.01 |
R7464:Six4
|
UTSW |
12 |
73,159,304 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7832:Six4
|
UTSW |
12 |
73,159,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Six4
|
UTSW |
12 |
73,151,013 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R7873:Six4
|
UTSW |
12 |
73,151,013 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R7956:Six4
|
UTSW |
12 |
73,150,535 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8266:Six4
|
UTSW |
12 |
73,155,423 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8728:Six4
|
UTSW |
12 |
73,159,180 (GRCm39) |
missense |
probably benign |
0.00 |
R9065:Six4
|
UTSW |
12 |
73,159,498 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9103:Six4
|
UTSW |
12 |
73,155,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Six4
|
UTSW |
12 |
73,155,681 (GRCm39) |
missense |
probably benign |
0.07 |
R9148:Six4
|
UTSW |
12 |
73,155,681 (GRCm39) |
missense |
probably benign |
0.07 |
R9430:Six4
|
UTSW |
12 |
73,150,719 (GRCm39) |
missense |
possibly damaging |
0.87 |
RF012:Six4
|
UTSW |
12 |
73,150,356 (GRCm39) |
frame shift |
probably null |
|
RF013:Six4
|
UTSW |
12 |
73,150,356 (GRCm39) |
frame shift |
probably null |
|
RF014:Six4
|
UTSW |
12 |
73,150,356 (GRCm39) |
frame shift |
probably null |
|
RF015:Six4
|
UTSW |
12 |
73,150,356 (GRCm39) |
frame shift |
probably null |
|
|