Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630073D07Rik |
AGGTGGTGGTGGTGGTGGTGGTGG |
AGGTGGTGGTGGTGGTGGTGG |
6: 132,603,479 (GRCm39) |
|
probably benign |
Het |
A930009A15Rik |
A |
T |
10: 115,414,194 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,741,221 (GRCm39) |
Y81C |
probably damaging |
Het |
Alx3 |
A |
T |
3: 107,508,022 (GRCm39) |
Y177F |
probably damaging |
Het |
C6 |
A |
G |
15: 4,764,717 (GRCm39) |
T138A |
probably benign |
Het |
Cacna2d3 |
T |
C |
14: 28,905,538 (GRCm39) |
M410V |
probably benign |
Het |
Ccn4 |
A |
G |
15: 66,791,137 (GRCm39) |
Y313C |
probably damaging |
Het |
Celsr3 |
G |
A |
9: 108,719,751 (GRCm39) |
R2450H |
probably benign |
Het |
Cnrip1 |
C |
T |
11: 17,004,845 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
A |
C |
9: 105,741,868 (GRCm39) |
D2350E |
probably damaging |
Het |
Cyp4a12b |
A |
G |
4: 115,292,167 (GRCm39) |
I407V |
probably benign |
Het |
Gpx4 |
A |
G |
10: 79,892,023 (GRCm39) |
I245V |
probably benign |
Het |
H2-K2 |
A |
G |
17: 34,218,499 (GRCm39) |
I139T |
probably benign |
Het |
Hmgcl |
A |
G |
4: 135,687,298 (GRCm39) |
K191R |
probably benign |
Het |
Hpdl |
A |
G |
4: 116,677,729 (GRCm39) |
V244A |
possibly damaging |
Het |
Hpse |
A |
G |
5: 100,840,104 (GRCm39) |
S338P |
probably damaging |
Het |
Ifi203 |
T |
C |
1: 173,762,646 (GRCm39) |
K162R |
possibly damaging |
Het |
Kit |
A |
G |
5: 75,799,810 (GRCm39) |
N514S |
probably damaging |
Het |
Kmt2d |
G |
A |
15: 98,742,030 (GRCm39) |
|
probably benign |
Het |
Limd1 |
T |
A |
9: 123,309,439 (GRCm39) |
S379R |
possibly damaging |
Het |
Llph |
A |
G |
10: 120,064,060 (GRCm39) |
K59E |
probably benign |
Het |
Lrrc7 |
T |
A |
3: 157,869,593 (GRCm39) |
M709L |
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,352,238 (GRCm39) |
S665G |
probably benign |
Het |
Ncapd3 |
C |
T |
9: 26,963,931 (GRCm39) |
H524Y |
probably benign |
Het |
Nfix |
CAAAAA |
CAAAA |
8: 85,442,876 (GRCm39) |
|
probably null |
Het |
Or51s1 |
T |
C |
7: 102,558,239 (GRCm39) |
D269G |
probably benign |
Het |
Phtf2 |
T |
C |
5: 20,987,296 (GRCm39) |
E400G |
probably damaging |
Het |
Pkd1l3 |
T |
C |
8: 110,362,949 (GRCm39) |
V1080A |
probably damaging |
Het |
Plch1 |
A |
T |
3: 63,606,944 (GRCm39) |
H1007Q |
probably benign |
Het |
Prr5 |
T |
C |
15: 84,565,417 (GRCm39) |
S3P |
probably damaging |
Het |
Qtrt1 |
G |
A |
9: 21,330,636 (GRCm39) |
D279N |
probably damaging |
Het |
Shc4 |
A |
T |
2: 125,565,251 (GRCm39) |
V16E |
probably damaging |
Het |
Sik3 |
A |
T |
9: 46,106,120 (GRCm39) |
L329F |
possibly damaging |
Het |
Slc36a3 |
A |
G |
11: 55,015,982 (GRCm39) |
S391P |
possibly damaging |
Het |
Smad1 |
C |
A |
8: 80,066,399 (GRCm39) |
R426L |
probably damaging |
Het |
Tent4b |
G |
A |
8: 88,969,957 (GRCm39) |
E210K |
probably damaging |
Het |
Thrap3 |
A |
T |
4: 126,061,293 (GRCm39) |
N820K |
possibly damaging |
Het |
Tnrc6b |
T |
C |
15: 80,807,841 (GRCm39) |
S1598P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,545,168 (GRCm39) |
I32645V |
probably damaging |
Het |
Zfp266 |
A |
C |
9: 20,410,777 (GRCm39) |
Y467D |
probably damaging |
Het |
Zfp526 |
T |
A |
7: 24,925,628 (GRCm39) |
M629K |
probably damaging |
Het |
Zfp788 |
A |
T |
7: 41,299,152 (GRCm39) |
H596L |
probably damaging |
Het |
Zhx3 |
A |
G |
2: 160,622,368 (GRCm39) |
W600R |
possibly damaging |
Het |
|
Other mutations in Rundc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Rundc1
|
APN |
11 |
101,325,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Rundc1
|
APN |
11 |
101,324,968 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02112:Rundc1
|
APN |
11 |
101,324,425 (GRCm39) |
missense |
probably benign |
0.01 |
R0379:Rundc1
|
UTSW |
11 |
101,315,973 (GRCm39) |
missense |
probably benign |
0.01 |
R1847:Rundc1
|
UTSW |
11 |
101,324,507 (GRCm39) |
missense |
probably benign |
|
R1959:Rundc1
|
UTSW |
11 |
101,322,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Rundc1
|
UTSW |
11 |
101,316,157 (GRCm39) |
missense |
probably benign |
0.34 |
R2225:Rundc1
|
UTSW |
11 |
101,322,170 (GRCm39) |
splice site |
probably benign |
|
R2323:Rundc1
|
UTSW |
11 |
101,316,101 (GRCm39) |
missense |
probably damaging |
0.98 |
R4599:Rundc1
|
UTSW |
11 |
101,324,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Rundc1
|
UTSW |
11 |
101,324,830 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4871:Rundc1
|
UTSW |
11 |
101,324,874 (GRCm39) |
missense |
probably benign |
0.18 |
R5054:Rundc1
|
UTSW |
11 |
101,315,967 (GRCm39) |
missense |
probably benign |
0.00 |
R5058:Rundc1
|
UTSW |
11 |
101,316,363 (GRCm39) |
missense |
probably benign |
|
R6349:Rundc1
|
UTSW |
11 |
101,324,988 (GRCm39) |
missense |
probably benign |
0.07 |
R6965:Rundc1
|
UTSW |
11 |
101,324,737 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7240:Rundc1
|
UTSW |
11 |
101,322,374 (GRCm39) |
critical splice donor site |
probably null |
|
R7286:Rundc1
|
UTSW |
11 |
101,320,413 (GRCm39) |
missense |
probably benign |
0.00 |
R7624:Rundc1
|
UTSW |
11 |
101,324,305 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8243:Rundc1
|
UTSW |
11 |
101,316,384 (GRCm39) |
missense |
probably benign |
0.00 |
R8322:Rundc1
|
UTSW |
11 |
101,322,992 (GRCm39) |
missense |
probably benign |
0.01 |
R8401:Rundc1
|
UTSW |
11 |
101,324,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R8934:Rundc1
|
UTSW |
11 |
101,322,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R9081:Rundc1
|
UTSW |
11 |
101,316,053 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Rundc1
|
UTSW |
11 |
101,324,560 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rundc1
|
UTSW |
11 |
101,322,948 (GRCm39) |
missense |
probably benign |
0.00 |
|