Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik2 |
T |
G |
11: 48,910,480 (GRCm39) |
D651A |
probably damaging |
Het |
Abcb1a |
A |
G |
5: 8,788,738 (GRCm39) |
N1039S |
probably benign |
Het |
Abcc2 |
G |
T |
19: 43,786,885 (GRCm39) |
V169F |
possibly damaging |
Het |
Adcy8 |
T |
C |
15: 64,597,384 (GRCm39) |
|
probably benign |
Het |
Aida |
C |
A |
1: 183,085,610 (GRCm39) |
|
probably null |
Het |
Armc8 |
A |
G |
9: 99,402,550 (GRCm39) |
I333T |
probably damaging |
Het |
B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,892,628 (GRCm39) |
D264G |
probably damaging |
Het |
Cenpf |
A |
G |
1: 189,381,009 (GRCm39) |
S2804P |
possibly damaging |
Het |
Cic |
A |
G |
7: 24,986,406 (GRCm39) |
D1276G |
probably damaging |
Het |
Cldn19 |
T |
C |
4: 119,114,094 (GRCm39) |
S79P |
possibly damaging |
Het |
Ctdp1 |
G |
A |
18: 80,493,428 (GRCm39) |
Q356* |
probably null |
Het |
Cyp2c69 |
A |
G |
19: 39,839,667 (GRCm39) |
|
probably benign |
Het |
Dhrs3 |
T |
C |
4: 144,620,281 (GRCm39) |
|
probably null |
Het |
Fhod3 |
T |
A |
18: 25,223,815 (GRCm39) |
W1054R |
probably damaging |
Het |
Gfral |
G |
A |
9: 76,100,725 (GRCm39) |
R238* |
probably null |
Het |
Gm10322 |
C |
A |
10: 59,451,941 (GRCm39) |
D19E |
possibly damaging |
Het |
Gprc6a |
CAAA |
CA |
10: 51,491,776 (GRCm39) |
|
probably null |
Het |
Idh3a |
T |
C |
9: 54,493,810 (GRCm39) |
S4P |
possibly damaging |
Het |
Il15ra |
G |
T |
2: 11,735,458 (GRCm39) |
|
probably null |
Het |
Ipo8 |
A |
T |
6: 148,707,842 (GRCm39) |
|
probably null |
Het |
Iqgap1 |
G |
A |
7: 80,366,835 (GRCm39) |
T1595I |
possibly damaging |
Het |
Kalrn |
C |
T |
16: 34,212,400 (GRCm39) |
|
probably null |
Het |
Klrb1a |
T |
C |
6: 128,595,466 (GRCm39) |
D96G |
probably benign |
Het |
Lrp1b |
C |
T |
2: 40,587,454 (GRCm39) |
V165M |
unknown |
Het |
Lrp4 |
A |
C |
2: 91,320,811 (GRCm39) |
T975P |
possibly damaging |
Het |
Lsm14a |
T |
A |
7: 34,053,204 (GRCm39) |
I283F |
probably damaging |
Het |
Mael |
T |
C |
1: 166,066,135 (GRCm39) |
D34G |
probably damaging |
Het |
Map2 |
C |
T |
1: 66,455,015 (GRCm39) |
Q1302* |
probably null |
Het |
Mctp1 |
T |
C |
13: 76,972,999 (GRCm39) |
|
probably null |
Het |
Mlxip |
T |
C |
5: 123,585,537 (GRCm39) |
V642A |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,657,547 (GRCm39) |
E1066G |
possibly damaging |
Het |
Naa35 |
T |
A |
13: 59,765,846 (GRCm39) |
|
probably benign |
Het |
Nacc1 |
T |
A |
8: 85,403,828 (GRCm39) |
I16F |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,963,645 (GRCm39) |
N499K |
probably benign |
Het |
Or10ab4 |
A |
G |
7: 107,655,004 (GRCm39) |
M272V |
possibly damaging |
Het |
Osbpl10 |
C |
A |
9: 115,036,655 (GRCm39) |
P253Q |
probably benign |
Het |
Ptpn21 |
G |
T |
12: 98,654,800 (GRCm39) |
S722R |
probably benign |
Het |
Rab44 |
C |
T |
17: 29,358,843 (GRCm39) |
P344S |
probably benign |
Het |
Rbms2 |
C |
T |
10: 127,979,312 (GRCm39) |
R139Q |
probably damaging |
Het |
Sh3bp2 |
T |
C |
5: 34,709,002 (GRCm39) |
Y32H |
probably damaging |
Het |
Slc6a15 |
A |
G |
10: 103,229,275 (GRCm39) |
I105V |
probably benign |
Het |
Thumpd3 |
A |
G |
6: 113,032,652 (GRCm39) |
D130G |
possibly damaging |
Het |
Trib1 |
A |
G |
15: 59,526,210 (GRCm39) |
Y260C |
probably damaging |
Het |
Tsks |
G |
T |
7: 44,601,309 (GRCm39) |
R208L |
possibly damaging |
Het |
Ttn |
G |
T |
2: 76,577,585 (GRCm39) |
S22690* |
probably null |
Het |
Ttyh2 |
T |
G |
11: 114,609,958 (GRCm39) |
S510A |
possibly damaging |
Het |
Was |
G |
T |
X: 7,952,927 (GRCm39) |
S271R |
probably benign |
Het |
Zfp267 |
T |
A |
3: 36,213,725 (GRCm39) |
C20S |
possibly damaging |
Het |
Zfp472 |
T |
A |
17: 33,196,685 (GRCm39) |
Y253* |
probably null |
Het |
|
Other mutations in Ccdc92b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0550:Ccdc92b
|
UTSW |
11 |
74,520,771 (GRCm39) |
splice site |
probably null |
|
R1944:Ccdc92b
|
UTSW |
11 |
74,520,835 (GRCm39) |
missense |
probably benign |
0.16 |
R1945:Ccdc92b
|
UTSW |
11 |
74,520,835 (GRCm39) |
missense |
probably benign |
0.16 |
R4382:Ccdc92b
|
UTSW |
11 |
74,520,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R5057:Ccdc92b
|
UTSW |
11 |
74,528,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:Ccdc92b
|
UTSW |
11 |
74,528,838 (GRCm39) |
missense |
probably benign |
0.08 |
R7107:Ccdc92b
|
UTSW |
11 |
74,520,887 (GRCm39) |
missense |
probably damaging |
0.99 |
R9631:Ccdc92b
|
UTSW |
11 |
74,520,845 (GRCm39) |
missense |
|
|
Z1186:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1187:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1188:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1189:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1190:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1191:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1192:Ccdc92b
|
UTSW |
11 |
74,520,880 (GRCm39) |
missense |
possibly damaging |
0.52 |
|