Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429P17Rik |
C |
A |
13: 48,114,201 (GRCm39) |
|
noncoding transcript |
Het |
9930012K11Rik |
T |
C |
14: 70,394,629 (GRCm39) |
E175G |
probably benign |
Het |
A630091E08Rik |
A |
G |
7: 98,192,814 (GRCm39) |
|
noncoding transcript |
Het |
Atm |
A |
T |
9: 53,390,973 (GRCm39) |
L1867Q |
probably damaging |
Het |
Atp5f1a |
A |
G |
18: 77,865,267 (GRCm39) |
D63G |
possibly damaging |
Het |
Baz2b |
A |
T |
2: 59,836,474 (GRCm39) |
S20T |
unknown |
Het |
C1qtnf7 |
G |
A |
5: 43,766,503 (GRCm39) |
C34Y |
possibly damaging |
Het |
Cactin |
A |
G |
10: 81,159,559 (GRCm39) |
T353A |
probably benign |
Het |
Cdyl |
A |
G |
13: 35,867,786 (GRCm39) |
K21E |
possibly damaging |
Het |
Crispld1 |
A |
G |
1: 17,799,022 (GRCm39) |
T48A |
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,701,918 (GRCm39) |
T1722S |
possibly damaging |
Het |
Dapk1 |
A |
T |
13: 60,877,345 (GRCm39) |
E528V |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,779,164 (GRCm39) |
D549G |
probably benign |
Het |
Dnajc5b |
C |
A |
3: 19,628,905 (GRCm39) |
N66K |
probably damaging |
Het |
Dusp16 |
G |
T |
6: 134,697,524 (GRCm39) |
R250S |
probably damaging |
Het |
F10 |
A |
G |
8: 13,105,551 (GRCm39) |
N384S |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,085,647 (GRCm39) |
S331G |
probably damaging |
Het |
Gm12185 |
A |
C |
11: 48,798,717 (GRCm39) |
I592S |
probably benign |
Het |
Gm9755 |
T |
C |
8: 67,967,312 (GRCm39) |
|
noncoding transcript |
Het |
Hspg2 |
T |
C |
4: 137,245,746 (GRCm39) |
L913P |
probably damaging |
Het |
Ifna1 |
T |
A |
4: 88,768,566 (GRCm39) |
S81R |
probably benign |
Het |
Iqgap2 |
T |
C |
13: 95,826,293 (GRCm39) |
K510E |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lhx6 |
A |
G |
2: 35,992,913 (GRCm39) |
Y140H |
probably damaging |
Het |
Lix1 |
A |
G |
17: 17,677,420 (GRCm39) |
H205R |
probably damaging |
Het |
Masp2 |
A |
T |
4: 148,698,490 (GRCm39) |
T524S |
probably benign |
Het |
Mndal |
A |
C |
1: 173,701,958 (GRCm39) |
F115V |
possibly damaging |
Het |
Morc3 |
C |
A |
16: 93,663,421 (GRCm39) |
N541K |
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Myocd |
A |
G |
11: 65,087,220 (GRCm39) |
S236P |
probably benign |
Het |
Nes |
T |
A |
3: 87,884,984 (GRCm39) |
V1037E |
probably benign |
Het |
Nfkbil1 |
A |
G |
17: 35,440,140 (GRCm39) |
W178R |
probably damaging |
Het |
Nobox |
A |
T |
6: 43,284,146 (GRCm39) |
C8* |
probably null |
Het |
Nwd1 |
A |
G |
8: 73,393,657 (GRCm39) |
T348A |
possibly damaging |
Het |
Or1e23 |
T |
C |
11: 73,407,546 (GRCm39) |
T160A |
probably damaging |
Het |
Or5bw2 |
T |
C |
7: 6,573,673 (GRCm39) |
S228P |
probably damaging |
Het |
Or8k17 |
A |
G |
2: 86,066,430 (GRCm39) |
S243P |
probably damaging |
Het |
Osbp2 |
T |
C |
11: 3,667,167 (GRCm39) |
T448A |
probably benign |
Het |
Plrg1 |
A |
G |
3: 82,966,070 (GRCm39) |
D75G |
probably benign |
Het |
Ppp1r8 |
T |
C |
4: 132,556,748 (GRCm39) |
E213G |
probably benign |
Het |
Rad54l2 |
A |
G |
9: 106,580,828 (GRCm39) |
F898L |
possibly damaging |
Het |
Rapgef6 |
TG |
TGG |
11: 54,437,223 (GRCm39) |
|
probably null |
Het |
Rasl10a |
G |
C |
11: 5,009,542 (GRCm39) |
R110P |
probably damaging |
Het |
Rttn |
T |
C |
18: 89,061,078 (GRCm39) |
I1082T |
probably benign |
Het |
Sema6d |
A |
G |
2: 124,506,265 (GRCm39) |
D734G |
possibly damaging |
Het |
Sgce |
C |
T |
6: 4,719,476 (GRCm39) |
V44M |
probably damaging |
Het |
Sgo2b |
A |
G |
8: 64,380,831 (GRCm39) |
V667A |
possibly damaging |
Het |
Shcbp1 |
A |
T |
8: 4,798,763 (GRCm39) |
C118* |
probably null |
Het |
Slain2 |
C |
T |
5: 73,133,347 (GRCm39) |
P563S |
probably damaging |
Het |
Slco1b2 |
A |
T |
6: 141,602,547 (GRCm39) |
I167F |
probably damaging |
Het |
Speg |
T |
C |
1: 75,399,621 (GRCm39) |
L2356P |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,118,164 (GRCm39) |
V305A |
probably benign |
Het |
Sspo |
G |
A |
6: 48,434,658 (GRCm39) |
R1050H |
probably benign |
Het |
Tmem106b |
A |
G |
6: 13,081,540 (GRCm39) |
N149S |
probably benign |
Het |
Tmem200a |
T |
C |
10: 25,868,812 (GRCm39) |
T486A |
probably damaging |
Het |
Tmem212 |
T |
A |
3: 27,939,250 (GRCm39) |
T79S |
possibly damaging |
Het |
Ttll11 |
A |
G |
2: 35,779,337 (GRCm39) |
V471A |
probably damaging |
Het |
Vill |
A |
G |
9: 118,899,769 (GRCm39) |
N318D |
probably benign |
Het |
Vmn2r102 |
A |
G |
17: 19,899,032 (GRCm39) |
D458G |
possibly damaging |
Het |
Zfp963 |
A |
T |
8: 70,196,837 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp472 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Zfp472
|
APN |
17 |
33,196,498 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03012:Zfp472
|
APN |
17 |
33,196,545 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03184:Zfp472
|
APN |
17 |
33,196,390 (GRCm39) |
nonsense |
probably null |
|
IGL03223:Zfp472
|
APN |
17 |
33,196,248 (GRCm39) |
missense |
probably benign |
0.03 |
R0421:Zfp472
|
UTSW |
17 |
33,194,897 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0463:Zfp472
|
UTSW |
17 |
33,194,936 (GRCm39) |
missense |
probably damaging |
0.98 |
R0614:Zfp472
|
UTSW |
17 |
33,196,908 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1348:Zfp472
|
UTSW |
17 |
33,196,794 (GRCm39) |
missense |
probably benign |
0.44 |
R1557:Zfp472
|
UTSW |
17 |
33,194,900 (GRCm39) |
missense |
probably benign |
0.32 |
R1725:Zfp472
|
UTSW |
17 |
33,196,311 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1856:Zfp472
|
UTSW |
17 |
33,184,887 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1964:Zfp472
|
UTSW |
17 |
33,196,848 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2115:Zfp472
|
UTSW |
17 |
33,196,988 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2249:Zfp472
|
UTSW |
17 |
33,197,109 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2252:Zfp472
|
UTSW |
17 |
33,195,257 (GRCm39) |
nonsense |
probably null |
|
R3709:Zfp472
|
UTSW |
17 |
33,196,685 (GRCm39) |
nonsense |
probably null |
|
R4119:Zfp472
|
UTSW |
17 |
33,197,189 (GRCm39) |
nonsense |
probably null |
|
R4406:Zfp472
|
UTSW |
17 |
33,197,134 (GRCm39) |
missense |
probably benign |
0.01 |
R4485:Zfp472
|
UTSW |
17 |
33,196,542 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4650:Zfp472
|
UTSW |
17 |
33,196,631 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4820:Zfp472
|
UTSW |
17 |
33,196,416 (GRCm39) |
missense |
probably benign |
0.01 |
R5369:Zfp472
|
UTSW |
17 |
33,196,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R5438:Zfp472
|
UTSW |
17 |
33,197,193 (GRCm39) |
missense |
probably damaging |
0.96 |
R5529:Zfp472
|
UTSW |
17 |
33,197,407 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5950:Zfp472
|
UTSW |
17 |
33,196,481 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6158:Zfp472
|
UTSW |
17 |
33,197,363 (GRCm39) |
nonsense |
probably null |
|
R7012:Zfp472
|
UTSW |
17 |
33,196,220 (GRCm39) |
missense |
probably benign |
0.00 |
R8108:Zfp472
|
UTSW |
17 |
33,196,977 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8290:Zfp472
|
UTSW |
17 |
33,197,088 (GRCm39) |
missense |
probably benign |
|
R8905:Zfp472
|
UTSW |
17 |
33,197,455 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9747:Zfp472
|
UTSW |
17 |
33,196,271 (GRCm39) |
missense |
possibly damaging |
0.53 |
|