Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
C |
A |
4: 124,504,181 (GRCm39) |
G124C |
unknown |
Het |
3425401B19Rik |
A |
T |
14: 32,384,239 (GRCm39) |
D575E |
possibly damaging |
Het |
Abca15 |
A |
T |
7: 119,939,272 (GRCm39) |
H222L |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,504,507 (GRCm39) |
V1013A |
probably benign |
Het |
Arsj |
T |
C |
3: 126,158,424 (GRCm39) |
M1T |
probably null |
Het |
Atp10a |
A |
C |
7: 58,478,088 (GRCm39) |
Q1377P |
probably benign |
Het |
Atrip |
T |
A |
9: 108,900,804 (GRCm39) |
E178D |
probably damaging |
Het |
Chadl |
T |
C |
15: 81,577,755 (GRCm39) |
N625D |
probably benign |
Het |
Chrng |
G |
A |
1: 87,137,523 (GRCm39) |
V320I |
probably benign |
Het |
Cox11 |
T |
C |
11: 90,535,221 (GRCm39) |
L84P |
probably damaging |
Het |
Dchs1 |
T |
G |
7: 105,410,132 (GRCm39) |
T1747P |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,597,227 (GRCm39) |
K3529E |
probably damaging |
Het |
Ecd |
T |
C |
14: 20,370,859 (GRCm39) |
N620S |
probably damaging |
Het |
Fbn1 |
T |
A |
2: 125,245,052 (GRCm39) |
K278N |
possibly damaging |
Het |
Fcho2 |
T |
C |
13: 98,926,275 (GRCm39) |
K103E |
probably damaging |
Het |
Fzd7 |
T |
G |
1: 59,522,419 (GRCm39) |
F101V |
probably damaging |
Het |
Galnt13 |
G |
T |
2: 54,406,491 (GRCm39) |
|
probably benign |
Het |
Gm32647 |
C |
T |
7: 94,124,939 (GRCm39) |
|
|
Het |
Gm5624 |
A |
T |
14: 44,797,333 (GRCm39) |
D152E |
probably benign |
Het |
Heatr6 |
T |
A |
11: 83,663,329 (GRCm39) |
V664E |
possibly damaging |
Het |
Hpgd |
A |
G |
8: 56,747,987 (GRCm39) |
D36G |
probably damaging |
Het |
Ifnlr1 |
A |
G |
4: 135,431,108 (GRCm39) |
T199A |
possibly damaging |
Het |
Kalrn |
T |
G |
16: 34,177,481 (GRCm39) |
D228A |
probably damaging |
Het |
Miox |
T |
C |
15: 89,219,524 (GRCm39) |
M47T |
probably damaging |
Het |
Nampt |
A |
T |
12: 32,880,301 (GRCm39) |
I65F |
probably benign |
Het |
Ncf1 |
T |
C |
5: 134,255,487 (GRCm39) |
K135E |
probably damaging |
Het |
Nop53 |
G |
A |
7: 15,672,314 (GRCm39) |
Q452* |
probably null |
Het |
Or8u10 |
A |
G |
2: 85,915,245 (GRCm39) |
L292S |
probably damaging |
Het |
Pik3cg |
A |
G |
12: 32,254,358 (GRCm39) |
V543A |
probably benign |
Het |
Ralgds |
T |
C |
2: 28,440,577 (GRCm39) |
|
probably null |
Het |
Rap1a |
A |
G |
3: 105,657,598 (GRCm39) |
V7A |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,813,543 (GRCm39) |
V639A |
possibly damaging |
Het |
Rassf8 |
A |
G |
6: 145,761,382 (GRCm39) |
N236S |
probably benign |
Het |
Rbm47 |
G |
C |
5: 66,183,626 (GRCm39) |
R326G |
probably damaging |
Het |
Sbno1 |
T |
C |
5: 124,516,554 (GRCm39) |
D1272G |
probably benign |
Het |
Setx |
A |
G |
2: 29,038,039 (GRCm39) |
D1508G |
probably benign |
Het |
Slc1a1 |
T |
A |
19: 28,882,810 (GRCm39) |
L358Q |
probably damaging |
Het |
Slc7a12 |
C |
A |
3: 14,564,186 (GRCm39) |
L20I |
probably benign |
Het |
Spata31g1 |
T |
C |
4: 42,972,853 (GRCm39) |
S729P |
probably damaging |
Het |
Spats2l |
C |
T |
1: 57,941,302 (GRCm39) |
T187M |
probably damaging |
Het |
Specc1l |
A |
G |
10: 75,082,494 (GRCm39) |
D647G |
probably benign |
Het |
Steap4 |
G |
A |
5: 8,028,562 (GRCm39) |
R380Q |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,952,099 (GRCm39) |
S456G |
probably benign |
Het |
Tfcp2 |
G |
T |
15: 100,410,194 (GRCm39) |
T391N |
probably damaging |
Het |
Tns2 |
T |
A |
15: 102,015,465 (GRCm39) |
D122E |
probably damaging |
Het |
Tshr |
A |
G |
12: 91,505,008 (GRCm39) |
M649V |
probably benign |
Het |
Ubr3 |
A |
G |
2: 69,824,107 (GRCm39) |
T1440A |
probably benign |
Het |
Urb2 |
A |
G |
8: 124,756,831 (GRCm39) |
D846G |
probably benign |
Het |
Vmn1r202 |
T |
C |
13: 22,685,632 (GRCm39) |
T262A |
possibly damaging |
Het |
Vmn2r61 |
G |
T |
7: 41,916,455 (GRCm39) |
W356L |
probably damaging |
Het |
Wdr11 |
T |
A |
7: 129,220,427 (GRCm39) |
M605K |
possibly damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
|
Other mutations in Cblif |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01604:Cblif
|
APN |
19 |
11,735,126 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02466:Cblif
|
APN |
19 |
11,729,596 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02678:Cblif
|
APN |
19 |
11,725,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Cblif
|
APN |
19 |
11,725,027 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0048:Cblif
|
UTSW |
19 |
11,727,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0048:Cblif
|
UTSW |
19 |
11,727,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0135:Cblif
|
UTSW |
19 |
11,735,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Cblif
|
UTSW |
19 |
11,729,658 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1758:Cblif
|
UTSW |
19 |
11,735,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Cblif
|
UTSW |
19 |
11,729,688 (GRCm39) |
missense |
probably benign |
|
R2054:Cblif
|
UTSW |
19 |
11,736,370 (GRCm39) |
missense |
probably benign |
0.01 |
R3087:Cblif
|
UTSW |
19 |
11,737,737 (GRCm39) |
nonsense |
probably null |
|
R4004:Cblif
|
UTSW |
19 |
11,736,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Cblif
|
UTSW |
19 |
11,729,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Cblif
|
UTSW |
19 |
11,729,583 (GRCm39) |
missense |
probably benign |
0.16 |
R5546:Cblif
|
UTSW |
19 |
11,725,859 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5795:Cblif
|
UTSW |
19 |
11,737,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R6147:Cblif
|
UTSW |
19 |
11,724,936 (GRCm39) |
start gained |
probably benign |
|
R7342:Cblif
|
UTSW |
19 |
11,740,587 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Cblif
|
UTSW |
19 |
11,727,551 (GRCm39) |
missense |
probably benign |
0.14 |
R8382:Cblif
|
UTSW |
19 |
11,727,090 (GRCm39) |
missense |
probably benign |
0.15 |
R8792:Cblif
|
UTSW |
19 |
11,727,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Cblif
|
UTSW |
19 |
11,737,748 (GRCm39) |
nonsense |
probably null |
|
R9230:Cblif
|
UTSW |
19 |
11,737,748 (GRCm39) |
nonsense |
probably null |
|
R9428:Cblif
|
UTSW |
19 |
11,735,102 (GRCm39) |
missense |
probably benign |
0.00 |
|