Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025C18Rik |
T |
G |
2: 164,920,864 (GRCm39) |
E56D |
unknown |
Het |
9930111J21Rik2 |
T |
C |
11: 48,910,543 (GRCm39) |
Q630R |
probably benign |
Het |
Abca9 |
A |
G |
11: 110,054,098 (GRCm39) |
V68A |
probably benign |
Het |
Acnat1 |
G |
A |
4: 49,449,181 (GRCm39) |
A195V |
possibly damaging |
Het |
Acsl3 |
C |
T |
1: 78,681,305 (GRCm39) |
A612V |
probably benign |
Het |
Adam12 |
A |
T |
7: 133,599,961 (GRCm39) |
D115E |
probably benign |
Het |
Adam3 |
T |
A |
8: 25,197,513 (GRCm39) |
|
probably null |
Het |
Aif1 |
G |
A |
17: 35,391,600 (GRCm39) |
|
probably benign |
Het |
Ank3 |
A |
G |
10: 69,824,139 (GRCm39) |
D154G |
probably damaging |
Het |
Arid3b |
A |
G |
9: 57,717,442 (GRCm39) |
C233R |
probably benign |
Het |
Ccdc7b |
T |
A |
8: 129,799,146 (GRCm39) |
D74E |
unknown |
Het |
Chpf |
T |
C |
1: 75,451,939 (GRCm39) |
H667R |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,931,263 (GRCm39) |
E1426G |
probably benign |
Het |
Dync1h1 |
A |
G |
12: 110,609,590 (GRCm39) |
I2791V |
probably benign |
Het |
Ehd3 |
A |
G |
17: 74,123,387 (GRCm39) |
N130S |
probably benign |
Het |
Fgfr4 |
A |
G |
13: 55,306,964 (GRCm39) |
T218A |
probably benign |
Het |
Foxe1 |
G |
A |
4: 46,344,599 (GRCm39) |
E136K |
possibly damaging |
Het |
Frmpd1 |
A |
G |
4: 45,284,478 (GRCm39) |
S1100G |
probably benign |
Het |
Gask1b |
G |
A |
3: 79,793,591 (GRCm39) |
A20T |
probably benign |
Het |
Gm21886 |
T |
G |
18: 80,132,972 (GRCm39) |
Q62P |
probably null |
Het |
Golga4 |
A |
G |
9: 118,385,434 (GRCm39) |
E852G |
probably damaging |
Het |
Gprin3 |
T |
C |
6: 59,330,696 (GRCm39) |
D537G |
probably benign |
Het |
Gpx5 |
C |
A |
13: 21,472,918 (GRCm39) |
D139Y |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,468,940 (GRCm39) |
Y5007C |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,235,832 (GRCm39) |
R1450* |
probably null |
Het |
Kif21a |
G |
A |
15: 90,840,517 (GRCm39) |
P1200S |
probably damaging |
Het |
Kmt2c |
G |
A |
5: 25,505,109 (GRCm39) |
R3400C |
probably damaging |
Het |
Miox |
A |
C |
15: 89,220,742 (GRCm39) |
M216L |
probably benign |
Het |
Mphosph9 |
T |
C |
5: 124,428,967 (GRCm39) |
Y687C |
probably damaging |
Het |
Mxi1 |
T |
A |
19: 53,299,192 (GRCm39) |
V21D |
probably benign |
Het |
Nbeal1 |
T |
C |
1: 60,299,591 (GRCm39) |
L1309P |
probably benign |
Het |
Onecut2 |
T |
A |
18: 64,474,046 (GRCm39) |
M180K |
possibly damaging |
Het |
Or10ag54 |
A |
T |
2: 87,099,421 (GRCm39) |
T99S |
possibly damaging |
Het |
Or13c25 |
C |
T |
4: 52,911,663 (GRCm39) |
V44I |
probably benign |
Het |
Or4c100 |
G |
A |
2: 88,356,289 (GRCm39) |
V121I |
probably benign |
Het |
Or7g22 |
T |
C |
9: 19,049,141 (GRCm39) |
M284T |
possibly damaging |
Het |
Polq |
A |
G |
16: 36,848,244 (GRCm39) |
T284A |
probably damaging |
Het |
Polrmt |
A |
T |
10: 79,577,714 (GRCm39) |
M295K |
probably damaging |
Het |
Pou2af1 |
G |
T |
9: 51,144,297 (GRCm39) |
M70I |
probably damaging |
Het |
Pou3f1 |
G |
A |
4: 124,552,232 (GRCm39) |
E245K |
probably damaging |
Het |
Psmb1 |
C |
T |
17: 15,714,748 (GRCm39) |
V50I |
probably benign |
Het |
Ptgis |
T |
C |
2: 167,069,434 (GRCm39) |
D50G |
probably damaging |
Het |
R3hdm2 |
A |
G |
10: 127,334,443 (GRCm39) |
I955M |
probably benign |
Het |
Rasef |
G |
A |
4: 73,677,935 (GRCm39) |
T97I |
probably benign |
Het |
Rasef |
T |
C |
4: 73,709,201 (GRCm39) |
T11A |
probably benign |
Het |
Sema4c |
C |
A |
1: 36,588,995 (GRCm39) |
L710F |
probably damaging |
Het |
Slc39a10 |
C |
T |
1: 46,851,328 (GRCm39) |
A721T |
probably damaging |
Het |
Sltm |
C |
G |
9: 70,493,955 (GRCm39) |
P802R |
possibly damaging |
Het |
Spata31d1a |
A |
G |
13: 59,848,139 (GRCm39) |
C1330R |
possibly damaging |
Het |
Susd1 |
T |
C |
4: 59,349,915 (GRCm39) |
D560G |
possibly damaging |
Het |
Tnfrsf1b |
T |
C |
4: 144,955,660 (GRCm39) |
Y32C |
probably damaging |
Het |
Trhr2 |
C |
A |
8: 123,084,083 (GRCm39) |
V306F |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,754,074 (GRCm39) |
Q35L |
probably benign |
Het |
Ttbk2 |
A |
G |
2: 120,616,510 (GRCm39) |
S197P |
probably damaging |
Het |
Uggt2 |
T |
A |
14: 119,280,059 (GRCm39) |
E806D |
probably benign |
Het |
Ushbp1 |
T |
G |
8: 71,841,422 (GRCm39) |
Q469P |
possibly damaging |
Het |
Vmn1r73 |
G |
A |
7: 11,491,036 (GRCm39) |
V285I |
possibly damaging |
Het |
Zfp934 |
A |
C |
13: 62,668,003 (GRCm39) |
S63R |
probably benign |
Het |
|
Other mutations in Cckbr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Cckbr
|
APN |
7 |
105,083,449 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01630:Cckbr
|
APN |
7 |
105,083,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01931:Cckbr
|
APN |
7 |
105,075,310 (GRCm39) |
missense |
probably benign |
|
IGL01955:Cckbr
|
APN |
7 |
105,084,169 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02219:Cckbr
|
APN |
7 |
105,083,255 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Cckbr
|
APN |
7 |
105,083,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Cckbr
|
APN |
7 |
105,083,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02878:Cckbr
|
APN |
7 |
105,083,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02946:Cckbr
|
APN |
7 |
105,083,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03179:Cckbr
|
APN |
7 |
105,084,130 (GRCm39) |
missense |
probably benign |
0.02 |
FR4548:Cckbr
|
UTSW |
7 |
105,083,888 (GRCm39) |
small deletion |
probably benign |
|
R0380:Cckbr
|
UTSW |
7 |
105,084,198 (GRCm39) |
missense |
probably benign |
0.00 |
R1767:Cckbr
|
UTSW |
7 |
105,083,758 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3890:Cckbr
|
UTSW |
7 |
105,075,376 (GRCm39) |
missense |
probably benign |
0.00 |
R3892:Cckbr
|
UTSW |
7 |
105,075,376 (GRCm39) |
missense |
probably benign |
0.00 |
R5116:Cckbr
|
UTSW |
7 |
105,082,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5589:Cckbr
|
UTSW |
7 |
105,083,732 (GRCm39) |
missense |
probably damaging |
0.98 |
R5975:Cckbr
|
UTSW |
7 |
105,119,826 (GRCm39) |
missense |
probably benign |
0.07 |
R6797:Cckbr
|
UTSW |
7 |
105,083,773 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6940:Cckbr
|
UTSW |
7 |
105,084,103 (GRCm39) |
missense |
probably benign |
0.00 |
R7194:Cckbr
|
UTSW |
7 |
105,084,552 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7293:Cckbr
|
UTSW |
7 |
105,083,852 (GRCm39) |
missense |
probably benign |
0.05 |
R7581:Cckbr
|
UTSW |
7 |
105,082,993 (GRCm39) |
missense |
probably benign |
0.05 |
R7793:Cckbr
|
UTSW |
7 |
105,082,798 (GRCm39) |
missense |
probably benign |
0.00 |
R8435:Cckbr
|
UTSW |
7 |
105,075,280 (GRCm39) |
missense |
probably benign |
|
RF009:Cckbr
|
UTSW |
7 |
105,083,893 (GRCm39) |
frame shift |
probably null |
|
RF039:Cckbr
|
UTSW |
7 |
105,083,893 (GRCm39) |
frame shift |
probably null |
|
RF062:Cckbr
|
UTSW |
7 |
105,083,894 (GRCm39) |
frame shift |
probably null |
|
|