Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010300C02Rik |
A |
T |
1: 37,626,012 (GRCm38) |
Y268* |
probably null |
Het |
Abca14 |
A |
T |
7: 120,289,460 (GRCm38) |
I1210F |
probably benign |
Het |
Ankrd17 |
T |
C |
5: 90,285,846 (GRCm38) |
H688R |
possibly damaging |
Het |
Arhgap24 |
T |
A |
5: 102,664,106 (GRCm38) |
N66K |
probably damaging |
Het |
Atp1a1 |
C |
T |
3: 101,590,466 (GRCm38) |
G335D |
probably damaging |
Het |
Cacna1g |
C |
T |
11: 94,459,555 (GRCm38) |
R488H |
possibly damaging |
Het |
Cacna1h |
A |
T |
17: 25,397,620 (GRCm38) |
V149E |
probably damaging |
Het |
Cd22 |
G |
T |
7: 30,873,170 (GRCm38) |
P338Q |
probably benign |
Het |
Cntln |
G |
T |
4: 85,096,839 (GRCm38) |
M1122I |
probably benign |
Het |
Cntrl |
A |
G |
2: 35,122,756 (GRCm38) |
N302S |
probably benign |
Het |
Cog8 |
T |
C |
8: 107,052,896 (GRCm38) |
R250G |
probably damaging |
Het |
Creld2 |
T |
C |
15: 88,823,753 (GRCm38) |
C232R |
probably damaging |
Het |
Cyp2b23 |
G |
A |
7: 26,673,149 (GRCm38) |
P347L |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,403,542 (GRCm38) |
|
probably null |
Het |
Eml6 |
C |
T |
11: 30,024,459 (GRCm38) |
V40I |
probably damaging |
Het |
Epb42 |
C |
T |
2: 121,029,967 (GRCm38) |
|
probably null |
Het |
Fcrla |
A |
G |
1: 170,921,004 (GRCm38) |
L190P |
probably damaging |
Het |
Galnt18 |
A |
T |
7: 111,779,428 (GRCm38) |
Y40* |
probably null |
Het |
Gdf7 |
A |
T |
12: 8,298,073 (GRCm38) |
M416K |
probably damaging |
Het |
Gm11232 |
T |
A |
4: 71,756,919 (GRCm38) |
|
probably null |
Het |
Gpam |
T |
A |
19: 55,088,176 (GRCm38) |
N198Y |
probably damaging |
Het |
Grip1 |
C |
T |
10: 119,986,350 (GRCm38) |
S327F |
possibly damaging |
Het |
Hey2 |
C |
T |
10: 30,834,356 (GRCm38) |
A134T |
probably benign |
Het |
Kat6a |
T |
C |
8: 22,938,652 (GRCm38) |
I1341T |
probably benign |
Het |
Kcnd3 |
T |
C |
3: 105,668,186 (GRCm38) |
L542P |
probably benign |
Het |
Lars |
G |
A |
18: 42,210,050 (GRCm38) |
R1101C |
probably damaging |
Het |
Lman2 |
T |
C |
13: 55,351,251 (GRCm38) |
D234G |
probably benign |
Het |
Map3k19 |
A |
C |
1: 127,817,898 (GRCm38) |
I1273R |
probably damaging |
Het |
Matn1 |
T |
A |
4: 130,950,019 (GRCm38) |
F180I |
possibly damaging |
Het |
Meikin |
T |
A |
11: 54,370,941 (GRCm38) |
L61* |
probably null |
Het |
Mroh2b |
G |
T |
15: 4,925,684 (GRCm38) |
D720Y |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,331,046 (GRCm38) |
I199T |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,248,461 (GRCm38) |
S535T |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,213,065 (GRCm38) |
M1715T |
probably damaging |
Het |
Nat8 |
A |
T |
6: 85,830,989 (GRCm38) |
V54D |
probably damaging |
Het |
Nbea |
A |
G |
3: 56,085,327 (GRCm38) |
V286A |
probably damaging |
Het |
Ndnf |
A |
G |
6: 65,704,014 (GRCm38) |
K426E |
possibly damaging |
Het |
Nup210l |
T |
A |
3: 90,190,972 (GRCm38) |
N1410K |
possibly damaging |
Het |
Oca2 |
A |
T |
7: 56,321,521 (GRCm38) |
T399S |
probably damaging |
Het |
Olfr1045 |
A |
G |
2: 86,198,252 (GRCm38) |
S167P |
probably damaging |
Het |
Olfr118 |
A |
T |
17: 37,672,925 (GRCm38) |
K301* |
probably null |
Het |
Olfr250 |
G |
A |
9: 38,368,196 (GRCm38) |
V217I |
probably benign |
Het |
Olfr366 |
A |
C |
2: 37,219,659 (GRCm38) |
T57P |
possibly damaging |
Het |
Olfr644 |
A |
T |
7: 104,068,459 (GRCm38) |
C191S |
probably damaging |
Het |
Olfr652 |
T |
A |
7: 104,565,071 (GRCm38) |
N283K |
probably damaging |
Het |
Otogl |
A |
C |
10: 107,878,152 (GRCm38) |
|
probably null |
Het |
Pde4b |
C |
T |
4: 102,605,176 (GRCm38) |
T511I |
probably damaging |
Het |
Proser3 |
A |
G |
7: 30,539,747 (GRCm38) |
|
probably null |
Het |
Psmd12 |
G |
A |
11: 107,479,646 (GRCm38) |
V24M |
probably damaging |
Het |
Rbm17 |
A |
T |
2: 11,593,461 (GRCm38) |
M170K |
probably benign |
Het |
Rims2 |
C |
T |
15: 39,511,314 (GRCm38) |
T1064I |
possibly damaging |
Het |
Ripor3 |
C |
T |
2: 167,992,653 (GRCm38) |
V281M |
probably damaging |
Het |
Rreb1 |
C |
A |
13: 37,946,928 (GRCm38) |
Q1353K |
possibly damaging |
Het |
Sgo2a |
A |
G |
1: 58,015,806 (GRCm38) |
D383G |
probably benign |
Het |
Sik3 |
C |
T |
9: 46,221,148 (GRCm38) |
T1346M |
probably damaging |
Het |
Slx1b |
A |
T |
7: 126,692,796 (GRCm38) |
V63E |
probably damaging |
Het |
Son |
A |
G |
16: 91,657,086 (GRCm38) |
D907G |
probably damaging |
Het |
Src |
G |
A |
2: 157,469,212 (GRCm38) |
V401M |
probably damaging |
Het |
St3gal4 |
T |
C |
9: 35,054,757 (GRCm38) |
K24E |
possibly damaging |
Het |
Stat6 |
A |
G |
10: 127,658,245 (GRCm38) |
K647R |
probably damaging |
Het |
Tbl1xr1 |
G |
A |
3: 22,193,169 (GRCm38) |
|
probably null |
Het |
Tlk2 |
G |
A |
11: 105,256,952 (GRCm38) |
|
probably null |
Het |
Tmbim6 |
T |
A |
15: 99,401,615 (GRCm38) |
I3K |
probably benign |
Het |
Tmeff2 |
A |
T |
1: 51,181,867 (GRCm38) |
I334F |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,840,315 (GRCm38) |
|
probably null |
Het |
Ubl7 |
T |
A |
9: 57,914,611 (GRCm38) |
I81N |
probably damaging |
Het |
Ugt1a10 |
A |
G |
1: 88,055,711 (GRCm38) |
Y77C |
probably damaging |
Het |
Uqcrfs1 |
A |
G |
13: 30,540,907 (GRCm38) |
C217R |
probably damaging |
Het |
Usp50 |
T |
C |
2: 126,761,634 (GRCm38) |
T331A |
probably benign |
Het |
Vmn1r65 |
A |
G |
7: 6,009,157 (GRCm38) |
V26A |
probably benign |
Het |
Wdfy3 |
A |
C |
5: 101,917,579 (GRCm38) |
V1241G |
possibly damaging |
Het |
Wtap |
A |
C |
17: 12,981,744 (GRCm38) |
|
probably null |
Het |
Zfp57 |
T |
C |
17: 37,006,098 (GRCm38) |
S20P |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 81,024,479 (GRCm38) |
D397G |
probably damaging |
Het |
Zfp747 |
A |
T |
7: 127,374,504 (GRCm38) |
S165T |
probably benign |
Het |
Zfp949 |
C |
T |
9: 88,569,838 (GRCm38) |
T487I |
probably damaging |
Het |
Zscan4d |
A |
G |
7: 11,164,994 (GRCm38) |
C119R |
probably damaging |
Het |
|
Other mutations in Zbtb40 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00473:Zbtb40
|
APN |
4 |
136,987,340 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00573:Zbtb40
|
APN |
4 |
137,018,078 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00774:Zbtb40
|
APN |
4 |
136,994,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R0046:Zbtb40
|
UTSW |
4 |
136,987,278 (GRCm38) |
missense |
probably damaging |
1.00 |
R0046:Zbtb40
|
UTSW |
4 |
136,987,278 (GRCm38) |
missense |
probably damaging |
1.00 |
R0334:Zbtb40
|
UTSW |
4 |
136,986,556 (GRCm38) |
missense |
probably damaging |
1.00 |
R0393:Zbtb40
|
UTSW |
4 |
137,018,531 (GRCm38) |
missense |
probably benign |
0.09 |
R0482:Zbtb40
|
UTSW |
4 |
136,983,228 (GRCm38) |
missense |
probably damaging |
1.00 |
R1846:Zbtb40
|
UTSW |
4 |
137,007,839 (GRCm38) |
missense |
probably benign |
0.00 |
R2153:Zbtb40
|
UTSW |
4 |
136,991,635 (GRCm38) |
missense |
probably damaging |
1.00 |
R2206:Zbtb40
|
UTSW |
4 |
137,017,285 (GRCm38) |
nonsense |
probably null |
|
R2291:Zbtb40
|
UTSW |
4 |
136,985,017 (GRCm38) |
missense |
possibly damaging |
0.78 |
R2406:Zbtb40
|
UTSW |
4 |
136,998,568 (GRCm38) |
missense |
probably benign |
0.34 |
R3707:Zbtb40
|
UTSW |
4 |
136,999,568 (GRCm38) |
missense |
probably damaging |
1.00 |
R4131:Zbtb40
|
UTSW |
4 |
136,995,396 (GRCm38) |
missense |
probably benign |
0.00 |
R4243:Zbtb40
|
UTSW |
4 |
137,018,549 (GRCm38) |
missense |
probably benign |
0.00 |
R4424:Zbtb40
|
UTSW |
4 |
136,998,694 (GRCm38) |
missense |
probably damaging |
0.96 |
R4725:Zbtb40
|
UTSW |
4 |
137,018,761 (GRCm38) |
utr 5 prime |
probably benign |
|
R4784:Zbtb40
|
UTSW |
4 |
137,007,097 (GRCm38) |
missense |
probably damaging |
1.00 |
R4795:Zbtb40
|
UTSW |
4 |
136,998,642 (GRCm38) |
missense |
probably benign |
0.00 |
R4796:Zbtb40
|
UTSW |
4 |
136,998,642 (GRCm38) |
missense |
probably benign |
0.00 |
R4838:Zbtb40
|
UTSW |
4 |
137,001,216 (GRCm38) |
missense |
probably benign |
0.15 |
R4859:Zbtb40
|
UTSW |
4 |
136,988,759 (GRCm38) |
missense |
probably damaging |
0.98 |
R4883:Zbtb40
|
UTSW |
4 |
137,000,930 (GRCm38) |
missense |
probably benign |
0.09 |
R5001:Zbtb40
|
UTSW |
4 |
136,996,150 (GRCm38) |
missense |
probably damaging |
1.00 |
R5030:Zbtb40
|
UTSW |
4 |
136,997,952 (GRCm38) |
missense |
probably benign |
0.00 |
R5060:Zbtb40
|
UTSW |
4 |
137,001,293 (GRCm38) |
missense |
possibly damaging |
0.71 |
R5529:Zbtb40
|
UTSW |
4 |
136,983,163 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5536:Zbtb40
|
UTSW |
4 |
136,987,331 (GRCm38) |
missense |
probably damaging |
1.00 |
R5589:Zbtb40
|
UTSW |
4 |
136,995,283 (GRCm38) |
missense |
probably damaging |
1.00 |
R6114:Zbtb40
|
UTSW |
4 |
136,988,691 (GRCm38) |
missense |
probably damaging |
1.00 |
R6393:Zbtb40
|
UTSW |
4 |
136,984,866 (GRCm38) |
missense |
probably null |
|
R7208:Zbtb40
|
UTSW |
4 |
136,999,626 (GRCm38) |
splice site |
probably null |
|
R7406:Zbtb40
|
UTSW |
4 |
137,000,894 (GRCm38) |
missense |
probably benign |
0.29 |
R7722:Zbtb40
|
UTSW |
4 |
136,991,518 (GRCm38) |
missense |
probably damaging |
0.98 |
R7803:Zbtb40
|
UTSW |
4 |
137,017,327 (GRCm38) |
missense |
probably benign |
|
R8292:Zbtb40
|
UTSW |
4 |
136,999,567 (GRCm38) |
missense |
probably damaging |
1.00 |
R8735:Zbtb40
|
UTSW |
4 |
136,998,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R8890:Zbtb40
|
UTSW |
4 |
136,998,586 (GRCm38) |
missense |
probably damaging |
1.00 |
R9003:Zbtb40
|
UTSW |
4 |
137,018,593 (GRCm38) |
missense |
probably damaging |
1.00 |
R9290:Zbtb40
|
UTSW |
4 |
137,018,218 (GRCm38) |
missense |
probably benign |
0.00 |
R9328:Zbtb40
|
UTSW |
4 |
137,018,309 (GRCm38) |
missense |
probably benign |
0.00 |
RF014:Zbtb40
|
UTSW |
4 |
137,017,306 (GRCm38) |
missense |
probably benign |
0.20 |
Z1176:Zbtb40
|
UTSW |
4 |
136,995,463 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Zbtb40
|
UTSW |
4 |
137,018,024 (GRCm38) |
nonsense |
probably null |
|
|