Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
A |
G |
8: 41,208,521 (GRCm39) |
T596A |
probably benign |
Het |
Adamts6 |
A |
G |
13: 104,450,207 (GRCm39) |
I303V |
probably damaging |
Het |
Alpl |
A |
T |
4: 137,471,112 (GRCm39) |
H341Q |
probably damaging |
Het |
Cachd1 |
G |
A |
4: 100,845,325 (GRCm39) |
R939H |
probably damaging |
Het |
Cd22 |
G |
A |
7: 30,569,494 (GRCm39) |
R541C |
probably benign |
Het |
Cenpf |
A |
T |
1: 189,391,801 (GRCm39) |
M660K |
probably benign |
Het |
Cmya5 |
A |
T |
13: 93,231,888 (GRCm39) |
S1067T |
possibly damaging |
Het |
Col5a2 |
C |
T |
1: 45,461,147 (GRCm39) |
G250D |
probably damaging |
Het |
Cylc2 |
C |
T |
4: 51,229,651 (GRCm39) |
T331M |
unknown |
Het |
Dgka |
A |
G |
10: 128,568,962 (GRCm39) |
M201T |
probably benign |
Het |
Dnajc13 |
T |
C |
9: 104,048,004 (GRCm39) |
I1804V |
probably benign |
Het |
Dym |
T |
A |
18: 75,419,754 (GRCm39) |
Y642N |
probably damaging |
Het |
Efr3b |
A |
T |
12: 4,050,886 (GRCm39) |
D26E |
probably damaging |
Het |
Emilin1 |
A |
T |
5: 31,075,040 (GRCm39) |
K427M |
possibly damaging |
Het |
Fam187b |
T |
C |
7: 30,676,659 (GRCm39) |
L56S |
probably benign |
Het |
Fbh1 |
C |
T |
2: 11,760,469 (GRCm39) |
V694I |
probably benign |
Het |
Fgd2 |
C |
T |
17: 29,597,997 (GRCm39) |
T644I |
probably benign |
Het |
G6pc1 |
T |
G |
11: 101,265,533 (GRCm39) |
|
probably null |
Het |
Gli2 |
A |
G |
1: 118,764,417 (GRCm39) |
S1245P |
probably benign |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Ighv1-84 |
T |
C |
12: 115,944,524 (GRCm39) |
D50G |
probably benign |
Het |
Impdh1 |
C |
A |
6: 29,216,214 (GRCm39) |
|
probably benign |
Het |
Inhca |
C |
T |
9: 103,136,627 (GRCm39) |
A525T |
probably benign |
Het |
Irf4 |
A |
T |
13: 30,945,433 (GRCm39) |
D393V |
possibly damaging |
Het |
Kalrn |
A |
G |
16: 34,181,305 (GRCm39) |
L111P |
probably damaging |
Het |
Lrch3 |
T |
C |
16: 32,802,223 (GRCm39) |
V58A |
possibly damaging |
Het |
Lrif1 |
C |
T |
3: 106,640,097 (GRCm39) |
T394I |
probably damaging |
Het |
Map4k1 |
A |
G |
7: 28,693,498 (GRCm39) |
T434A |
probably benign |
Het |
Mcur1 |
G |
A |
13: 43,695,193 (GRCm39) |
T327M |
probably damaging |
Het |
Myo9b |
G |
T |
8: 71,786,966 (GRCm39) |
S716I |
probably benign |
Het |
Nol10 |
T |
A |
12: 17,419,772 (GRCm39) |
|
probably benign |
Het |
Nos3 |
A |
G |
5: 24,573,841 (GRCm39) |
T202A |
possibly damaging |
Het |
Odad1 |
A |
G |
7: 45,597,116 (GRCm39) |
T456A |
probably benign |
Het |
Or14j7 |
T |
C |
17: 38,235,168 (GRCm39) |
V237A |
probably benign |
Het |
Or2d4 |
A |
C |
7: 106,543,905 (GRCm39) |
M101R |
probably benign |
Het |
Parp12 |
A |
T |
6: 39,094,856 (GRCm39) |
S80T |
probably benign |
Het |
Pde1a |
C |
T |
2: 79,758,086 (GRCm39) |
V50I |
probably benign |
Het |
Pfkl |
A |
T |
10: 77,833,356 (GRCm39) |
|
probably null |
Het |
Phkg1 |
A |
T |
5: 129,895,056 (GRCm39) |
Y207N |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,535,728 (GRCm39) |
T640A |
possibly damaging |
Het |
Pip5k1c |
C |
A |
10: 81,147,827 (GRCm39) |
H411N |
probably damaging |
Het |
Pla2g4e |
A |
G |
2: 120,075,172 (GRCm39) |
S73P |
probably damaging |
Het |
Polr2b |
T |
C |
5: 77,483,510 (GRCm39) |
V662A |
probably damaging |
Het |
Prss43 |
C |
T |
9: 110,658,494 (GRCm39) |
R265C |
possibly damaging |
Het |
Rap1b |
A |
T |
10: 117,658,746 (GRCm39) |
V29D |
probably damaging |
Het |
Rraga |
A |
G |
4: 86,495,048 (GRCm39) |
E298G |
probably damaging |
Het |
Rrp8 |
A |
T |
7: 105,382,781 (GRCm39) |
I418N |
probably damaging |
Het |
Siglecf |
T |
C |
7: 43,005,030 (GRCm39) |
V420A |
probably benign |
Het |
Snx14 |
T |
A |
9: 88,297,746 (GRCm39) |
N174I |
probably damaging |
Het |
Spopfm2 |
T |
C |
3: 94,083,427 (GRCm39) |
D128G |
probably benign |
Het |
Teddm3 |
A |
G |
16: 20,971,685 (GRCm39) |
*295Q |
probably null |
Het |
Tfap2c |
A |
G |
2: 172,393,926 (GRCm39) |
D245G |
possibly damaging |
Het |
Tfap2d |
A |
G |
1: 19,178,508 (GRCm39) |
N191S |
probably benign |
Het |
Tmt1b |
A |
T |
10: 128,796,476 (GRCm39) |
M111K |
possibly damaging |
Het |
Unc80 |
A |
G |
1: 66,651,427 (GRCm39) |
R1591G |
possibly damaging |
Het |
Vmn1r116 |
T |
C |
7: 20,606,616 (GRCm39) |
W146R |
probably damaging |
Het |
Vps13b |
C |
G |
15: 35,925,535 (GRCm39) |
S3823R |
probably damaging |
Het |
Wiz |
T |
A |
17: 32,586,821 (GRCm39) |
D163V |
probably damaging |
Het |
Xylt1 |
G |
C |
7: 116,980,594 (GRCm39) |
A61P |
unknown |
Het |
Zfp521 |
A |
C |
18: 13,978,701 (GRCm39) |
F571V |
probably damaging |
Het |
Zfp664 |
T |
A |
5: 124,963,133 (GRCm39) |
C176S |
possibly damaging |
Het |
Zfyve26 |
T |
C |
12: 79,334,227 (GRCm39) |
N264D |
probably benign |
Het |
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