Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
T |
7: 119,888,683 (GRCm39) |
I1210F |
probably benign |
Het |
Ankrd17 |
T |
C |
5: 90,433,705 (GRCm39) |
H688R |
possibly damaging |
Het |
Arhgap24 |
T |
A |
5: 102,811,972 (GRCm39) |
N66K |
probably damaging |
Het |
Atp1a1 |
C |
T |
3: 101,497,782 (GRCm39) |
G335D |
probably damaging |
Het |
Cacna1g |
C |
T |
11: 94,350,381 (GRCm39) |
R488H |
possibly damaging |
Het |
Cacna1h |
A |
T |
17: 25,616,594 (GRCm39) |
V149E |
probably damaging |
Het |
Cd22 |
G |
T |
7: 30,572,595 (GRCm39) |
P338Q |
probably benign |
Het |
Cntln |
G |
T |
4: 85,015,076 (GRCm39) |
M1122I |
probably benign |
Het |
Cntrl |
A |
G |
2: 35,012,768 (GRCm39) |
N302S |
probably benign |
Het |
Cog8 |
T |
C |
8: 107,779,528 (GRCm39) |
R250G |
probably damaging |
Het |
Cracdl |
A |
T |
1: 37,665,093 (GRCm39) |
Y268* |
probably null |
Het |
Creld2 |
T |
C |
15: 88,707,956 (GRCm39) |
C232R |
probably damaging |
Het |
Cyp2b23 |
G |
A |
7: 26,372,574 (GRCm39) |
P347L |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,403,688 (GRCm39) |
|
probably null |
Het |
Eml6 |
C |
T |
11: 29,974,459 (GRCm39) |
V40I |
probably damaging |
Het |
Epb42 |
C |
T |
2: 120,860,448 (GRCm39) |
|
probably null |
Het |
Fcrla |
A |
G |
1: 170,748,573 (GRCm39) |
L190P |
probably damaging |
Het |
Galnt18 |
A |
T |
7: 111,378,635 (GRCm39) |
Y40* |
probably null |
Het |
Gdf7 |
A |
T |
12: 8,348,073 (GRCm39) |
M416K |
probably damaging |
Het |
Gm11232 |
T |
A |
4: 71,675,156 (GRCm39) |
|
probably null |
Het |
Gpam |
T |
A |
19: 55,076,608 (GRCm39) |
N198Y |
probably damaging |
Het |
Grip1 |
C |
T |
10: 119,822,255 (GRCm39) |
S327F |
possibly damaging |
Het |
Hey2 |
C |
T |
10: 30,710,352 (GRCm39) |
A134T |
probably benign |
Het |
Kat6a |
T |
C |
8: 23,428,668 (GRCm39) |
I1341T |
probably benign |
Het |
Kcnd3 |
T |
C |
3: 105,575,502 (GRCm39) |
L542P |
probably benign |
Het |
Lars1 |
G |
A |
18: 42,343,115 (GRCm39) |
R1101C |
probably damaging |
Het |
Lman2 |
T |
C |
13: 55,499,064 (GRCm39) |
D234G |
probably benign |
Het |
Map3k19 |
A |
C |
1: 127,745,635 (GRCm39) |
I1273R |
probably damaging |
Het |
Matn1 |
T |
A |
4: 130,677,330 (GRCm39) |
F180I |
possibly damaging |
Het |
Meikin |
T |
A |
11: 54,261,767 (GRCm39) |
L61* |
probably null |
Het |
Mroh2b |
G |
T |
15: 4,955,166 (GRCm39) |
D720Y |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,221,872 (GRCm39) |
I199T |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,139,287 (GRCm39) |
S535T |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,120,347 (GRCm39) |
M1715T |
probably damaging |
Het |
Nat8 |
A |
T |
6: 85,807,971 (GRCm39) |
V54D |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,992,748 (GRCm39) |
V286A |
probably damaging |
Het |
Nup210l |
T |
A |
3: 90,098,279 (GRCm39) |
N1410K |
possibly damaging |
Het |
Oca2 |
A |
T |
7: 55,971,269 (GRCm39) |
T399S |
probably damaging |
Het |
Or10al2 |
A |
T |
17: 37,983,816 (GRCm39) |
K301* |
probably null |
Het |
Or1af1 |
A |
C |
2: 37,109,671 (GRCm39) |
T57P |
possibly damaging |
Het |
Or51a43 |
A |
T |
7: 103,717,666 (GRCm39) |
C191S |
probably damaging |
Het |
Or52h7 |
T |
A |
7: 104,214,278 (GRCm39) |
N283K |
probably damaging |
Het |
Or8c10 |
G |
A |
9: 38,279,492 (GRCm39) |
V217I |
probably benign |
Het |
Or8j3 |
A |
G |
2: 86,028,596 (GRCm39) |
S167P |
probably damaging |
Het |
Otogl |
A |
C |
10: 107,714,013 (GRCm39) |
|
probably null |
Het |
Pde4b |
C |
T |
4: 102,462,373 (GRCm39) |
T511I |
probably damaging |
Het |
Proser3 |
A |
G |
7: 30,239,172 (GRCm39) |
|
probably null |
Het |
Psmd12 |
G |
A |
11: 107,370,472 (GRCm39) |
V24M |
probably damaging |
Het |
Rbm17 |
A |
T |
2: 11,598,272 (GRCm39) |
M170K |
probably benign |
Het |
Rims2 |
C |
T |
15: 39,374,710 (GRCm39) |
T1064I |
possibly damaging |
Het |
Ripor3 |
C |
T |
2: 167,834,573 (GRCm39) |
V281M |
probably damaging |
Het |
Rreb1 |
C |
A |
13: 38,130,904 (GRCm39) |
Q1353K |
possibly damaging |
Het |
Sgo2a |
A |
G |
1: 58,054,965 (GRCm39) |
D383G |
probably benign |
Het |
Sik3 |
C |
T |
9: 46,132,446 (GRCm39) |
T1346M |
probably damaging |
Het |
Slx1b |
A |
T |
7: 126,291,968 (GRCm39) |
V63E |
probably damaging |
Het |
Son |
A |
G |
16: 91,453,974 (GRCm39) |
D907G |
probably damaging |
Het |
Src |
G |
A |
2: 157,311,132 (GRCm39) |
V401M |
probably damaging |
Het |
St3gal4 |
T |
C |
9: 34,966,053 (GRCm39) |
K24E |
possibly damaging |
Het |
Stat6 |
A |
G |
10: 127,494,114 (GRCm39) |
K647R |
probably damaging |
Het |
Tbl1xr1 |
G |
A |
3: 22,247,333 (GRCm39) |
|
probably null |
Het |
Tlk2 |
G |
A |
11: 105,147,778 (GRCm39) |
|
probably null |
Het |
Tmbim6 |
T |
A |
15: 99,299,496 (GRCm39) |
I3K |
probably benign |
Het |
Tmeff2 |
A |
T |
1: 51,221,026 (GRCm39) |
I334F |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,670,659 (GRCm39) |
|
probably null |
Het |
Ubl7 |
T |
A |
9: 57,821,894 (GRCm39) |
I81N |
probably damaging |
Het |
Ugt1a10 |
A |
G |
1: 87,983,433 (GRCm39) |
Y77C |
probably damaging |
Het |
Uqcrfs1 |
A |
G |
13: 30,724,890 (GRCm39) |
C217R |
probably damaging |
Het |
Usp50 |
T |
C |
2: 126,603,554 (GRCm39) |
T331A |
probably benign |
Het |
Vmn1r65 |
A |
G |
7: 6,012,156 (GRCm39) |
V26A |
probably benign |
Het |
Wdfy3 |
A |
C |
5: 102,065,445 (GRCm39) |
V1241G |
possibly damaging |
Het |
Wtap |
A |
C |
17: 13,200,631 (GRCm39) |
|
probably null |
Het |
Zbtb40 |
C |
A |
4: 136,712,148 (GRCm39) |
A1187S |
possibly damaging |
Het |
Zfp57 |
T |
C |
17: 37,316,990 (GRCm39) |
S20P |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 80,674,227 (GRCm39) |
D397G |
probably damaging |
Het |
Zfp747 |
A |
T |
7: 126,973,676 (GRCm39) |
S165T |
probably benign |
Het |
Zfp949 |
C |
T |
9: 88,451,891 (GRCm39) |
T487I |
probably damaging |
Het |
Zscan4d |
A |
G |
7: 10,898,921 (GRCm39) |
C119R |
probably damaging |
Het |
|
Other mutations in Ndnf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00755:Ndnf
|
APN |
6 |
65,680,242 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01737:Ndnf
|
APN |
6 |
65,680,539 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03000:Ndnf
|
APN |
6 |
65,680,299 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03236:Ndnf
|
APN |
6 |
65,673,156 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL03373:Ndnf
|
APN |
6 |
65,681,272 (GRCm39) |
missense |
possibly damaging |
0.47 |
K3955:Ndnf
|
UTSW |
6 |
65,678,413 (GRCm39) |
splice site |
probably benign |
|
R1670:Ndnf
|
UTSW |
6 |
65,680,054 (GRCm39) |
missense |
probably benign |
0.00 |
R1687:Ndnf
|
UTSW |
6 |
65,680,407 (GRCm39) |
missense |
probably benign |
0.00 |
R1909:Ndnf
|
UTSW |
6 |
65,680,297 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3951:Ndnf
|
UTSW |
6 |
65,680,125 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4043:Ndnf
|
UTSW |
6 |
65,680,920 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4465:Ndnf
|
UTSW |
6 |
65,681,180 (GRCm39) |
missense |
probably benign |
|
R4983:Ndnf
|
UTSW |
6 |
65,680,555 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5271:Ndnf
|
UTSW |
6 |
65,680,650 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6785:Ndnf
|
UTSW |
6 |
65,680,047 (GRCm39) |
missense |
probably benign |
0.01 |
R7874:Ndnf
|
UTSW |
6 |
65,680,413 (GRCm39) |
missense |
probably benign |
|
R8049:Ndnf
|
UTSW |
6 |
65,680,414 (GRCm39) |
missense |
probably benign |
0.04 |
R8398:Ndnf
|
UTSW |
6 |
65,681,362 (GRCm39) |
missense |
probably damaging |
0.99 |
R8729:Ndnf
|
UTSW |
6 |
65,680,758 (GRCm39) |
nonsense |
probably null |
|
R8853:Ndnf
|
UTSW |
6 |
65,680,161 (GRCm39) |
missense |
probably benign |
0.06 |
R9567:Ndnf
|
UTSW |
6 |
65,681,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R9755:Ndnf
|
UTSW |
6 |
65,680,502 (GRCm39) |
missense |
probably benign |
|
RF017:Ndnf
|
UTSW |
6 |
65,681,313 (GRCm39) |
missense |
probably damaging |
0.97 |
X0066:Ndnf
|
UTSW |
6 |
65,678,501 (GRCm39) |
nonsense |
probably null |
|
|