Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankhd1 |
A |
G |
18: 36,791,465 (GRCm39) |
T154A |
|
Het |
Arhgap21 |
A |
G |
2: 20,854,007 (GRCm39) |
I1795T |
probably damaging |
Het |
Arhgef4 |
T |
C |
1: 34,850,762 (GRCm39) |
V436A |
probably benign |
Het |
Bche |
A |
T |
3: 73,609,149 (GRCm39) |
N92K |
probably damaging |
Het |
Bmp2 |
C |
T |
2: 133,403,105 (GRCm39) |
H219Y |
probably benign |
Het |
Cables1 |
T |
G |
18: 11,973,269 (GRCm39) |
V136G |
probably benign |
Het |
Cacna1d |
G |
A |
14: 29,769,270 (GRCm39) |
R1887* |
probably null |
Het |
Chrd |
A |
G |
16: 20,557,903 (GRCm39) |
E774G |
probably benign |
Het |
Chrna2 |
A |
G |
14: 66,388,525 (GRCm39) |
*513W |
probably null |
Het |
Cracr2b |
T |
C |
7: 141,044,161 (GRCm39) |
F131S |
probably damaging |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Cyfip1 |
T |
A |
7: 55,546,523 (GRCm39) |
I545N |
possibly damaging |
Het |
Enpp3 |
T |
A |
10: 24,654,717 (GRCm39) |
T654S |
possibly damaging |
Het |
Glce |
A |
G |
9: 61,968,228 (GRCm39) |
S308P |
probably damaging |
Het |
H3c13 |
C |
A |
3: 96,176,309 (GRCm39) |
Y100* |
probably null |
Het |
Hmmr |
A |
C |
11: 40,606,256 (GRCm39) |
|
probably null |
Het |
Hoxb9 |
A |
G |
11: 96,165,464 (GRCm39) |
N178D |
probably benign |
Het |
Igkv10-94 |
A |
T |
6: 68,681,595 (GRCm39) |
F82I |
probably damaging |
Het |
Igkv1-133 |
A |
T |
6: 67,702,578 (GRCm39) |
K99* |
probably null |
Het |
Il4i1 |
A |
G |
7: 44,489,819 (GRCm39) |
Q528R |
probably benign |
Het |
Inhba |
G |
T |
13: 16,201,572 (GRCm39) |
G378V |
possibly damaging |
Het |
Katna1 |
T |
C |
10: 7,614,623 (GRCm39) |
S44P |
probably benign |
Het |
Mgat4d |
T |
C |
8: 84,084,722 (GRCm39) |
V155A |
possibly damaging |
Het |
Morc2b |
C |
T |
17: 33,354,746 (GRCm39) |
E1009K |
possibly damaging |
Het |
Myo9a |
T |
A |
9: 59,695,721 (GRCm39) |
L341H |
probably damaging |
Het |
Nell2 |
C |
T |
15: 95,129,216 (GRCm39) |
D716N |
probably damaging |
Het |
Or1n2 |
A |
G |
2: 36,796,953 (GRCm39) |
|
probably benign |
Het |
Or5t16 |
A |
G |
2: 86,818,707 (GRCm39) |
V271A |
probably benign |
Het |
Or8g36 |
C |
T |
9: 39,422,810 (GRCm39) |
V69I |
probably benign |
Het |
Or8k30 |
A |
G |
2: 86,338,815 (GRCm39) |
H4R |
probably benign |
Het |
Ppp1r37 |
T |
C |
7: 19,265,868 (GRCm39) |
T633A |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,258,302 (GRCm39) |
K576E |
probably damaging |
Het |
Prl2c5 |
G |
T |
13: 13,360,469 (GRCm39) |
M45I |
probably benign |
Het |
Rigi |
C |
A |
4: 40,223,824 (GRCm39) |
G397* |
probably null |
Het |
Rnf44 |
A |
G |
13: 54,830,667 (GRCm39) |
S247P |
probably benign |
Het |
Scn3a |
A |
G |
2: 65,336,555 (GRCm39) |
F684L |
probably damaging |
Het |
Skint2 |
T |
A |
4: 112,502,648 (GRCm39) |
M286K |
probably benign |
Het |
Slc39a9 |
G |
A |
12: 80,713,450 (GRCm39) |
G116D |
probably damaging |
Het |
Smchd1 |
G |
A |
17: 71,762,621 (GRCm39) |
T206I |
possibly damaging |
Het |
Tmem161a |
C |
T |
8: 70,630,154 (GRCm39) |
|
probably benign |
Het |
Trpm6 |
T |
A |
19: 18,853,474 (GRCm39) |
H1831Q |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,667,614 (GRCm39) |
H792Q |
probably damaging |
Het |
Ttc6 |
A |
G |
12: 57,720,542 (GRCm39) |
Q936R |
possibly damaging |
Het |
Usp53 |
A |
T |
3: 122,756,531 (GRCm39) |
|
probably null |
Het |
Vmn1r236 |
T |
A |
17: 21,507,696 (GRCm39) |
C271* |
probably null |
Het |
Vmn2r70 |
T |
A |
7: 85,211,071 (GRCm39) |
M547L |
probably damaging |
Het |
Vwa5b1 |
G |
A |
4: 138,332,800 (GRCm39) |
T254M |
probably damaging |
Het |
Zc3h4 |
T |
C |
7: 16,163,770 (GRCm39) |
F655S |
unknown |
Het |
Zfp605 |
G |
A |
5: 110,275,316 (GRCm39) |
G145S |
probably benign |
Het |
|
Other mutations in Ldlrad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00793:Ldlrad1
|
APN |
4 |
107,075,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Ldlrad1
|
APN |
4 |
107,075,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03356:Ldlrad1
|
APN |
4 |
107,072,035 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0458:Ldlrad1
|
UTSW |
4 |
107,073,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R1556:Ldlrad1
|
UTSW |
4 |
107,075,010 (GRCm39) |
missense |
probably benign |
0.24 |
R1610:Ldlrad1
|
UTSW |
4 |
107,072,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R1996:Ldlrad1
|
UTSW |
4 |
107,072,158 (GRCm39) |
nonsense |
probably null |
|
R4510:Ldlrad1
|
UTSW |
4 |
107,066,715 (GRCm39) |
missense |
probably benign |
0.00 |
R4511:Ldlrad1
|
UTSW |
4 |
107,066,715 (GRCm39) |
missense |
probably benign |
0.00 |
R7000:Ldlrad1
|
UTSW |
4 |
107,066,777 (GRCm39) |
missense |
probably benign |
0.14 |
R7795:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R7797:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R7964:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R7990:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8004:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8005:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8007:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8077:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8078:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8088:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8089:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8130:Ldlrad1
|
UTSW |
4 |
107,066,688 (GRCm39) |
missense |
probably benign |
0.00 |
R8883:Ldlrad1
|
UTSW |
4 |
107,073,412 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Ldlrad1
|
UTSW |
4 |
107,072,086 (GRCm39) |
missense |
probably damaging |
0.99 |
|