Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
A |
11: 110,182,931 (GRCm39) |
E1042V |
probably benign |
Het |
Ahnak2 |
T |
C |
12: 112,747,750 (GRCm39) |
E1035G |
probably benign |
Het |
Aip |
T |
G |
19: 4,165,188 (GRCm39) |
D227A |
probably benign |
Het |
Ankrd13d |
T |
C |
19: 4,323,081 (GRCm39) |
H283R |
probably damaging |
Het |
Aox4 |
C |
T |
1: 58,303,094 (GRCm39) |
T1175I |
probably damaging |
Het |
Atn1 |
T |
C |
6: 124,723,700 (GRCm39) |
|
probably benign |
Het |
Camkk2 |
A |
G |
5: 122,902,187 (GRCm39) |
S41P |
probably damaging |
Het |
Ceacam16 |
G |
A |
7: 19,595,182 (GRCm39) |
|
probably benign |
Het |
Dcaf15 |
T |
C |
8: 84,824,626 (GRCm39) |
N524D |
possibly damaging |
Het |
Dcaf7 |
A |
T |
11: 105,928,077 (GRCm39) |
Y43F |
probably damaging |
Het |
Epha3 |
T |
C |
16: 63,433,287 (GRCm39) |
I453V |
probably benign |
Het |
Etv1 |
A |
T |
12: 38,915,640 (GRCm39) |
T413S |
possibly damaging |
Het |
Evx2 |
A |
C |
2: 74,489,606 (GRCm39) |
L53R |
probably damaging |
Het |
Fam168b |
G |
A |
1: 34,858,684 (GRCm39) |
A166V |
probably damaging |
Het |
Fancm |
A |
T |
12: 65,141,669 (GRCm39) |
Y430F |
probably benign |
Het |
Fyb2 |
A |
G |
4: 104,802,661 (GRCm39) |
T188A |
possibly damaging |
Het |
Gabbr1 |
T |
C |
17: 37,374,271 (GRCm39) |
I538T |
probably damaging |
Het |
Glyctk |
T |
A |
9: 106,033,691 (GRCm39) |
T208S |
possibly damaging |
Het |
Golga7 |
T |
C |
8: 23,735,904 (GRCm39) |
D114G |
probably damaging |
Het |
Grip1 |
T |
C |
10: 119,733,702 (GRCm39) |
|
probably null |
Het |
Gtf2f1 |
G |
T |
17: 57,311,161 (GRCm39) |
S351R |
probably damaging |
Het |
Hook2 |
T |
C |
8: 85,721,642 (GRCm39) |
L300P |
probably damaging |
Het |
Hsf4 |
A |
G |
8: 105,997,481 (GRCm39) |
S45G |
probably damaging |
Het |
Iars1 |
T |
A |
13: 49,876,190 (GRCm39) |
M825K |
probably damaging |
Het |
Kcnj2 |
A |
G |
11: 110,963,315 (GRCm39) |
I236V |
probably benign |
Het |
Large2 |
G |
A |
2: 92,197,433 (GRCm39) |
T354I |
probably benign |
Het |
Mak |
C |
A |
13: 41,206,828 (GRCm39) |
V101F |
probably benign |
Het |
Mylk2 |
A |
G |
2: 152,757,673 (GRCm39) |
|
probably null |
Het |
Myo18b |
A |
T |
5: 113,020,373 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,037,249 (GRCm39) |
H2955L |
probably benign |
Het |
Neurl1a |
G |
C |
19: 47,228,367 (GRCm39) |
G71A |
probably damaging |
Het |
Ogfrl1 |
A |
T |
1: 23,415,309 (GRCm39) |
L142Q |
probably damaging |
Het |
Or11g27 |
C |
A |
14: 50,771,612 (GRCm39) |
H248N |
probably damaging |
Het |
Or1e27-ps1 |
A |
G |
11: 73,556,160 (GRCm39) |
T242A |
probably damaging |
Het |
P3h4 |
C |
A |
11: 100,302,671 (GRCm39) |
A322S |
probably damaging |
Het |
Piwil2 |
A |
C |
14: 70,660,342 (GRCm39) |
|
probably null |
Het |
Pkd2l2 |
A |
G |
18: 34,561,297 (GRCm39) |
D435G |
probably damaging |
Het |
Plekha6 |
A |
G |
1: 133,207,145 (GRCm39) |
N567S |
probably null |
Het |
Prss54 |
G |
A |
8: 96,286,173 (GRCm39) |
P300L |
possibly damaging |
Het |
Pxdn |
G |
A |
12: 30,024,000 (GRCm39) |
R67Q |
probably damaging |
Het |
Rapgef3 |
C |
A |
15: 97,665,292 (GRCm39) |
|
probably benign |
Het |
Sec24b |
C |
T |
3: 129,782,550 (GRCm39) |
G1147S |
possibly damaging |
Het |
Sh2b3 |
A |
T |
5: 121,966,418 (GRCm39) |
|
probably null |
Het |
Sh3glb1 |
A |
T |
3: 144,397,664 (GRCm39) |
D358E |
probably damaging |
Het |
Shmt2 |
C |
T |
10: 127,353,731 (GRCm39) |
R478H |
probably benign |
Het |
Slc1a6 |
A |
G |
10: 78,637,671 (GRCm39) |
E399G |
probably benign |
Het |
Slc22a23 |
T |
A |
13: 34,528,542 (GRCm39) |
Y80F |
probably damaging |
Het |
Slc25a19 |
A |
G |
11: 115,506,377 (GRCm39) |
V272A |
probably benign |
Het |
Stk32a |
A |
T |
18: 43,446,474 (GRCm39) |
D308V |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,707,657 (GRCm39) |
I1698V |
possibly damaging |
Het |
Thoc5 |
G |
A |
11: 4,865,497 (GRCm39) |
V359M |
probably benign |
Het |
Tmpo |
C |
T |
10: 90,998,800 (GRCm39) |
R329H |
probably benign |
Het |
Trim8 |
T |
C |
19: 46,503,626 (GRCm39) |
S393P |
probably benign |
Het |
Vill |
A |
T |
9: 118,895,932 (GRCm39) |
Y103F |
probably damaging |
Het |
Zpld1 |
C |
T |
16: 55,053,962 (GRCm39) |
E277K |
probably damaging |
Het |
|
Other mutations in Zfp948 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01787:Zfp948
|
APN |
17 |
21,807,333 (GRCm39) |
missense |
probably benign |
0.01 |
R0212:Zfp948
|
UTSW |
17 |
21,808,422 (GRCm39) |
missense |
probably benign |
0.01 |
R0225:Zfp948
|
UTSW |
17 |
21,807,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Zfp948
|
UTSW |
17 |
21,807,764 (GRCm39) |
missense |
probably benign |
0.02 |
R0437:Zfp948
|
UTSW |
17 |
21,807,260 (GRCm39) |
missense |
unknown |
|
R0490:Zfp948
|
UTSW |
17 |
21,808,296 (GRCm39) |
missense |
probably benign |
0.02 |
R1245:Zfp948
|
UTSW |
17 |
21,807,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Zfp948
|
UTSW |
17 |
21,805,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Zfp948
|
UTSW |
17 |
21,807,953 (GRCm39) |
nonsense |
probably null |
|
R3692:Zfp948
|
UTSW |
17 |
21,807,838 (GRCm39) |
missense |
probably benign |
0.01 |
R4767:Zfp948
|
UTSW |
17 |
21,808,569 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5226:Zfp948
|
UTSW |
17 |
21,808,505 (GRCm39) |
missense |
probably benign |
0.00 |
R5753:Zfp948
|
UTSW |
17 |
21,807,156 (GRCm39) |
missense |
probably damaging |
0.97 |
R5766:Zfp948
|
UTSW |
17 |
21,805,078 (GRCm39) |
missense |
probably benign |
0.02 |
R5959:Zfp948
|
UTSW |
17 |
21,807,776 (GRCm39) |
missense |
probably benign |
0.01 |
R6291:Zfp948
|
UTSW |
17 |
21,807,286 (GRCm39) |
missense |
unknown |
|
R6312:Zfp948
|
UTSW |
17 |
21,807,429 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6482:Zfp948
|
UTSW |
17 |
21,807,813 (GRCm39) |
missense |
probably benign |
0.01 |
R7046:Zfp948
|
UTSW |
17 |
21,808,719 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7053:Zfp948
|
UTSW |
17 |
21,805,121 (GRCm39) |
nonsense |
probably null |
|
R7207:Zfp948
|
UTSW |
17 |
21,808,602 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7222:Zfp948
|
UTSW |
17 |
21,808,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R7460:Zfp948
|
UTSW |
17 |
21,808,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R7760:Zfp948
|
UTSW |
17 |
21,808,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R7818:Zfp948
|
UTSW |
17 |
21,807,985 (GRCm39) |
missense |
probably benign |
0.14 |
RF011:Zfp948
|
UTSW |
17 |
21,808,574 (GRCm39) |
missense |
probably damaging |
0.97 |
X0023:Zfp948
|
UTSW |
17 |
21,807,122 (GRCm39) |
missense |
probably benign |
0.01 |
|