Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
G |
T |
11: 101,417,359 |
Y10* |
probably null |
Het |
Aass |
C |
A |
6: 23,107,634 |
Q383H |
probably damaging |
Het |
Bag1 |
T |
C |
4: 40,936,657 |
D333G |
probably damaging |
Het |
Cap2 |
A |
G |
13: 46,639,949 |
|
probably benign |
Het |
Col27a1 |
G |
T |
4: 63,225,631 |
A519S |
probably benign |
Het |
Cr2 |
A |
G |
1: 195,159,595 |
V726A |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,480,845 |
|
probably benign |
Het |
Dennd4c |
A |
G |
4: 86,799,551 |
D595G |
possibly damaging |
Het |
Ercc2 |
G |
T |
7: 19,393,449 |
R340L |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,298,205 |
T35A |
probably benign |
Het |
Fndc3a |
A |
G |
14: 72,566,141 |
Y525H |
probably benign |
Het |
Gm4922 |
T |
C |
10: 18,784,047 |
Q309R |
probably benign |
Het |
Gm5263 |
T |
C |
1: 146,420,554 |
|
noncoding transcript |
Het |
Gm6563 |
A |
C |
19: 23,676,387 |
R180S |
probably damaging |
Het |
Gpr182 |
C |
A |
10: 127,750,864 |
V73F |
probably damaging |
Het |
Gramd1b |
C |
T |
9: 40,315,773 |
R179H |
probably damaging |
Het |
Hk1 |
C |
T |
10: 62,353,105 |
A10T |
probably benign |
Het |
Hmgn3 |
C |
A |
9: 83,110,384 |
|
probably benign |
Het |
Il1b |
C |
T |
2: 129,369,729 |
E24K |
probably damaging |
Het |
Itgb6 |
G |
T |
2: 60,627,985 |
Q475K |
probably benign |
Het |
Lrrc74b |
A |
G |
16: 17,545,558 |
S368P |
probably benign |
Het |
Mfsd2b |
T |
C |
12: 4,866,469 |
T234A |
possibly damaging |
Het |
Muc6 |
A |
T |
7: 141,651,062 |
Y270N |
probably damaging |
Het |
Olfr142 |
A |
T |
2: 90,252,132 |
Y285* |
probably null |
Het |
Pear1 |
G |
A |
3: 87,752,301 |
T742I |
probably damaging |
Het |
Peli2 |
G |
A |
14: 48,256,034 |
V238I |
probably benign |
Het |
Pira2 |
A |
G |
7: 3,844,612 |
L26P |
probably damaging |
Het |
Pot1b |
A |
G |
17: 55,662,521 |
V549A |
possibly damaging |
Het |
Prdm16 |
T |
C |
4: 154,347,927 |
Y295C |
probably benign |
Het |
Ptprd |
A |
T |
4: 76,140,507 |
|
probably benign |
Het |
Rap1gap |
A |
T |
4: 137,716,155 |
M145L |
probably benign |
Het |
Setd7 |
A |
T |
3: 51,532,967 |
|
probably benign |
Het |
Ssx2ip |
T |
C |
3: 146,428,010 |
I258T |
probably benign |
Het |
Stard9 |
T |
C |
2: 120,699,084 |
Y1941H |
possibly damaging |
Het |
Stxbp3 |
T |
C |
3: 108,800,152 |
E420G |
probably benign |
Het |
Tpra1 |
T |
C |
6: 88,909,342 |
V101A |
probably damaging |
Het |
Tpx2 |
G |
T |
2: 152,884,235 |
Q373H |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,727,008 |
R29914Q |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 70,003,465 |
|
probably null |
Het |
Usp18 |
G |
A |
6: 121,253,771 |
G53D |
probably damaging |
Het |
Vps13c |
A |
T |
9: 67,955,780 |
H3026L |
probably benign |
Het |
Zan |
T |
C |
5: 137,463,626 |
E1097G |
unknown |
Het |
|