Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
A |
G |
8: 73,208,962 (GRCm39) |
E364G |
probably benign |
Het |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Abcb4 |
A |
G |
5: 8,978,524 (GRCm39) |
T557A |
probably damaging |
Het |
Acadm |
C |
T |
3: 153,635,221 (GRCm39) |
E298K |
probably damaging |
Het |
Adrb3 |
T |
C |
8: 27,717,855 (GRCm39) |
|
probably null |
Het |
Aldh1b1 |
A |
G |
4: 45,803,128 (GRCm39) |
Y222C |
possibly damaging |
Het |
Ankrd6 |
A |
G |
4: 32,860,387 (GRCm39) |
Y19H |
probably damaging |
Het |
Arhgap21 |
T |
A |
2: 20,854,701 (GRCm39) |
T1554S |
probably benign |
Het |
BC043934 |
T |
C |
9: 96,319,173 (GRCm39) |
|
noncoding transcript |
Het |
Birc6 |
A |
G |
17: 74,901,319 (GRCm39) |
|
probably benign |
Het |
Blm |
A |
C |
7: 80,108,573 (GRCm39) |
F1357C |
probably benign |
Het |
Cd209a |
T |
C |
8: 3,797,713 (GRCm39) |
|
probably null |
Het |
Cdk7 |
G |
A |
13: 100,854,103 (GRCm39) |
H129Y |
probably damaging |
Het |
Clec14a |
G |
T |
12: 58,315,070 (GRCm39) |
P184Q |
probably damaging |
Het |
Cma1 |
T |
A |
14: 56,179,128 (GRCm39) |
I243F |
probably damaging |
Het |
Cntnap3 |
G |
T |
13: 64,909,798 (GRCm39) |
T769K |
possibly damaging |
Het |
Col5a1 |
A |
C |
2: 27,922,751 (GRCm39) |
K273T |
possibly damaging |
Het |
Csnk1e |
A |
G |
15: 79,309,129 (GRCm39) |
Y266H |
probably damaging |
Het |
Cyb5d1 |
A |
G |
11: 69,284,597 (GRCm39) |
L185S |
probably damaging |
Het |
Dennd5b |
T |
C |
6: 148,942,998 (GRCm39) |
|
probably null |
Het |
Dipk2a |
C |
A |
9: 94,419,486 (GRCm39) |
R148L |
probably benign |
Het |
Drp2 |
G |
A |
X: 133,342,065 (GRCm39) |
R567H |
probably damaging |
Homo |
Dzank1 |
T |
G |
2: 144,364,486 (GRCm39) |
D37A |
probably damaging |
Het |
Echdc2 |
A |
G |
4: 108,022,825 (GRCm39) |
I34V |
probably benign |
Het |
Esm1 |
A |
T |
13: 113,349,965 (GRCm39) |
R128S |
probably benign |
Het |
Fbh1 |
T |
A |
2: 11,769,041 (GRCm39) |
I251F |
probably damaging |
Het |
Fbrsl1 |
A |
G |
5: 110,595,817 (GRCm39) |
S73P |
probably damaging |
Het |
Fbxo6 |
A |
T |
4: 148,233,948 (GRCm39) |
S49R |
probably damaging |
Het |
Gm17093 |
A |
T |
14: 44,756,779 (GRCm39) |
Q82L |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,348,067 (GRCm39) |
|
probably null |
Het |
Hspa4l |
C |
A |
3: 40,700,081 (GRCm39) |
|
probably benign |
Het |
Il3ra |
G |
A |
14: 14,351,080 (GRCm38) |
A201T |
probably benign |
Het |
Irx5 |
T |
A |
8: 93,087,409 (GRCm39) |
V447E |
probably damaging |
Het |
Kif14 |
G |
T |
1: 136,410,697 (GRCm39) |
L668F |
probably damaging |
Het |
Lag3 |
T |
A |
6: 124,881,416 (GRCm39) |
R519W |
unknown |
Het |
Lgr4 |
A |
G |
2: 109,842,283 (GRCm39) |
N756S |
probably damaging |
Het |
Lingo4 |
T |
A |
3: 94,310,308 (GRCm39) |
H415Q |
probably benign |
Het |
Lingo4 |
A |
G |
3: 94,309,848 (GRCm39) |
H262R |
probably benign |
Het |
Lkaaear1 |
C |
A |
2: 181,339,376 (GRCm39) |
G25* |
probably null |
Het |
Maco1 |
A |
G |
4: 134,555,610 (GRCm39) |
Y288H |
probably damaging |
Het |
Marf1 |
T |
C |
16: 13,932,095 (GRCm39) |
K1641E |
probably benign |
Het |
Mtfmt |
T |
C |
9: 65,351,133 (GRCm39) |
|
probably benign |
Het |
Mtif3 |
G |
A |
5: 146,893,598 (GRCm39) |
T203M |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,407,430 (GRCm39) |
I2740T |
probably benign |
Het |
Nrdc |
A |
G |
4: 108,903,809 (GRCm39) |
T720A |
probably benign |
Het |
Or2d2 |
T |
C |
7: 106,728,271 (GRCm39) |
T110A |
probably benign |
Het |
Peak1 |
T |
A |
9: 56,148,560 (GRCm39) |
D32V |
possibly damaging |
Het |
Pigr |
G |
A |
1: 130,769,554 (GRCm39) |
D122N |
probably benign |
Het |
Plekhg3 |
A |
G |
12: 76,612,311 (GRCm39) |
R391G |
possibly damaging |
Het |
Ppfia3 |
T |
C |
7: 44,990,542 (GRCm39) |
D919G |
probably damaging |
Het |
Pramel23 |
T |
A |
4: 143,424,939 (GRCm39) |
Q168L |
possibly damaging |
Het |
Rnase2b |
T |
A |
14: 51,400,208 (GRCm39) |
D96E |
possibly damaging |
Het |
Rsf1 |
CGGCGGC |
CGGCGGCCGCGGCGGC |
7: 97,229,130 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Serpina3f |
A |
G |
12: 104,186,615 (GRCm39) |
T394A |
probably benign |
Het |
Six3 |
A |
G |
17: 85,928,720 (GRCm39) |
N18S |
possibly damaging |
Het |
Slc12a5 |
T |
A |
2: 164,825,285 (GRCm39) |
|
probably null |
Het |
Slc35f6 |
A |
G |
5: 30,805,427 (GRCm39) |
N21S |
probably damaging |
Het |
Slc39a6 |
A |
T |
18: 24,729,351 (GRCm39) |
I454N |
probably damaging |
Het |
Slc40a1 |
T |
A |
1: 45,948,824 (GRCm39) |
E485D |
probably damaging |
Het |
Sort1 |
G |
A |
3: 108,235,385 (GRCm39) |
C255Y |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,785,771 (GRCm39) |
T624S |
probably benign |
Het |
Taf4b |
T |
A |
18: 15,031,100 (GRCm39) |
I828N |
probably damaging |
Het |
Terf2 |
T |
C |
8: 107,803,110 (GRCm39) |
|
probably benign |
Het |
Timd4 |
C |
T |
11: 46,706,344 (GRCm39) |
R49C |
probably damaging |
Het |
Tpte |
T |
C |
8: 22,808,362 (GRCm39) |
S166P |
probably benign |
Het |
Trabd2b |
T |
C |
4: 114,264,052 (GRCm39) |
L13P |
probably benign |
Het |
Trappc11 |
A |
T |
8: 47,975,476 (GRCm39) |
Y247* |
probably null |
Het |
Trnt1 |
C |
T |
6: 106,755,853 (GRCm39) |
Q303* |
probably null |
Het |
Tspyl5 |
T |
A |
15: 33,687,201 (GRCm39) |
Q248L |
possibly damaging |
Het |
Ubxn7 |
A |
T |
16: 32,200,322 (GRCm39) |
K337N |
probably damaging |
Het |
Unc13a |
T |
A |
8: 72,095,816 (GRCm39) |
I1234F |
probably benign |
Het |
Vmn1r127 |
A |
T |
7: 21,052,943 (GRCm39) |
F282I |
probably damaging |
Het |
Wdhd1 |
A |
T |
14: 47,506,111 (GRCm39) |
|
probably null |
Het |
Zfp605 |
A |
G |
5: 110,275,352 (GRCm39) |
K157E |
probably damaging |
Het |
Zhx2 |
T |
A |
15: 57,684,755 (GRCm39) |
D41E |
probably benign |
Het |
|
Other mutations in Stk33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01137:Stk33
|
APN |
7 |
108,928,775 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01467:Stk33
|
APN |
7 |
108,928,796 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01558:Stk33
|
APN |
7 |
108,940,491 (GRCm39) |
intron |
probably benign |
|
IGL01775:Stk33
|
APN |
7 |
108,911,574 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0052:Stk33
|
UTSW |
7 |
108,878,876 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0336:Stk33
|
UTSW |
7 |
108,930,681 (GRCm39) |
missense |
probably benign |
0.01 |
R0394:Stk33
|
UTSW |
7 |
108,940,696 (GRCm39) |
missense |
probably benign |
|
R0579:Stk33
|
UTSW |
7 |
108,924,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R0727:Stk33
|
UTSW |
7 |
108,920,725 (GRCm39) |
missense |
probably damaging |
0.96 |
R1363:Stk33
|
UTSW |
7 |
108,879,028 (GRCm39) |
missense |
probably benign |
0.06 |
R1574:Stk33
|
UTSW |
7 |
108,879,027 (GRCm39) |
missense |
probably benign |
0.01 |
R1574:Stk33
|
UTSW |
7 |
108,879,027 (GRCm39) |
missense |
probably benign |
0.01 |
R2153:Stk33
|
UTSW |
7 |
108,940,527 (GRCm39) |
missense |
probably benign |
0.01 |
R4366:Stk33
|
UTSW |
7 |
108,879,002 (GRCm39) |
missense |
probably benign |
0.06 |
R4896:Stk33
|
UTSW |
7 |
108,926,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5283:Stk33
|
UTSW |
7 |
108,935,334 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6339:Stk33
|
UTSW |
7 |
108,920,672 (GRCm39) |
missense |
probably benign |
0.03 |
R6547:Stk33
|
UTSW |
7 |
108,920,042 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6717:Stk33
|
UTSW |
7 |
108,926,823 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6894:Stk33
|
UTSW |
7 |
108,935,269 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8975:Stk33
|
UTSW |
7 |
108,935,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Stk33
|
UTSW |
7 |
108,928,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R9175:Stk33
|
UTSW |
7 |
108,920,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:Stk33
|
UTSW |
7 |
108,940,686 (GRCm39) |
missense |
probably benign |
0.00 |
R9416:Stk33
|
UTSW |
7 |
108,940,689 (GRCm39) |
missense |
probably benign |
0.39 |
Z1176:Stk33
|
UTSW |
7 |
108,935,266 (GRCm39) |
missense |
possibly damaging |
0.51 |
|