Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438A13Rik |
C |
T |
3: 36,969,221 (GRCm38) |
T2233I |
possibly damaging |
Het |
9430038I01Rik |
T |
C |
7: 137,387,292 (GRCm38) |
|
probably benign |
Het |
Abhd14a |
A |
T |
9: 106,443,951 (GRCm38) |
|
probably null |
Het |
Actn2 |
T |
C |
13: 12,340,497 (GRCm38) |
N2D |
probably benign |
Het |
Adcy9 |
T |
C |
16: 4,311,567 (GRCm38) |
E722G |
probably damaging |
Het |
Alox12 |
C |
A |
11: 70,242,783 (GRCm38) |
V572L |
possibly damaging |
Het |
Ankrd11 |
T |
C |
8: 122,889,749 (GRCm38) |
I2434V |
possibly damaging |
Het |
Anks1 |
T |
A |
17: 27,991,447 (GRCm38) |
|
probably null |
Het |
Bpifa3 |
T |
A |
2: 154,136,321 (GRCm38) |
S148T |
probably damaging |
Het |
Bptf |
C |
T |
11: 107,035,864 (GRCm38) |
|
probably benign |
Het |
Cabin1 |
A |
T |
10: 75,657,839 (GRCm38) |
L1655H |
probably damaging |
Het |
Ccdc13 |
G |
T |
9: 121,827,235 (GRCm38) |
Q171K |
probably benign |
Het |
Ccdc33 |
T |
A |
9: 58,117,478 (GRCm38) |
Q155L |
possibly damaging |
Het |
Cckbr |
G |
A |
7: 105,470,619 (GRCm38) |
G280E |
probably benign |
Het |
Cdk11b |
G |
A |
4: 155,648,240 (GRCm38) |
|
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,919,038 (GRCm38) |
|
probably null |
Het |
Cenpj |
A |
T |
14: 56,564,066 (GRCm38) |
I150N |
possibly damaging |
Het |
Cep135 |
C |
A |
5: 76,640,890 (GRCm38) |
A1110E |
possibly damaging |
Het |
Chit1 |
C |
A |
1: 134,146,626 (GRCm38) |
H224N |
probably damaging |
Het |
Cul5 |
T |
C |
9: 53,622,793 (GRCm38) |
R680G |
probably damaging |
Het |
Dhx58 |
C |
A |
11: 100,702,209 (GRCm38) |
R224L |
probably damaging |
Het |
Dlx1 |
C |
A |
2: 71,531,009 (GRCm38) |
N122K |
probably damaging |
Het |
Dnah5 |
A |
C |
15: 28,234,282 (GRCm38) |
D279A |
probably damaging |
Het |
Enpp3 |
A |
G |
10: 24,774,842 (GRCm38) |
W799R |
probably benign |
Het |
Ercc5 |
A |
G |
1: 44,173,406 (GRCm38) |
T675A |
probably benign |
Het |
Farsa |
T |
A |
8: 84,864,432 (GRCm38) |
|
probably null |
Het |
Fbxw15 |
A |
T |
9: 109,555,252 (GRCm38) |
V397D |
probably damaging |
Het |
Fcrl5 |
G |
A |
3: 87,442,103 (GRCm38) |
V62I |
probably benign |
Het |
Gart |
A |
G |
16: 91,624,336 (GRCm38) |
S815P |
probably damaging |
Het |
Glrx5 |
A |
G |
12: 105,040,323 (GRCm38) |
N111S |
possibly damaging |
Het |
Gm10845 |
A |
G |
14: 79,863,174 (GRCm38) |
|
noncoding transcript |
Het |
Gm11639 |
A |
G |
11: 104,687,549 (GRCm38) |
|
probably benign |
Het |
Gm8882 |
A |
G |
6: 132,362,073 (GRCm38) |
S61P |
unknown |
Het |
Gm9925 |
T |
A |
18: 74,065,516 (GRCm38) |
|
probably benign |
Het |
Gsdme |
T |
C |
6: 50,227,359 (GRCm38) |
N206S |
probably benign |
Het |
Helz2 |
T |
C |
2: 181,231,050 (GRCm38) |
S2459G |
probably benign |
Het |
Hnrnpul1 |
A |
G |
7: 25,754,359 (GRCm38) |
S93P |
possibly damaging |
Het |
Ints2 |
A |
T |
11: 86,226,748 (GRCm38) |
I716N |
possibly damaging |
Het |
Lmnb2 |
G |
A |
10: 80,905,128 (GRCm38) |
Q248* |
probably null |
Het |
Map3k7cl |
A |
G |
16: 87,570,321 (GRCm38) |
I32V |
probably benign |
Het |
Mfsd4b4 |
A |
T |
10: 39,892,470 (GRCm38) |
I255N |
probably benign |
Het |
Myh6 |
A |
G |
14: 54,950,508 (GRCm38) |
I1163T |
probably benign |
Het |
Nphs1 |
A |
T |
7: 30,466,115 (GRCm38) |
T636S |
possibly damaging |
Het |
Ntsr1 |
T |
A |
2: 180,500,788 (GRCm38) |
L124Q |
probably damaging |
Het |
Obscn |
C |
T |
11: 59,122,619 (GRCm38) |
|
probably null |
Het |
P4ha2 |
G |
A |
11: 54,126,412 (GRCm38) |
|
probably null |
Het |
Pcdha9 |
T |
A |
18: 36,999,111 (GRCm38) |
V411D |
probably benign |
Het |
Pkhd1l1 |
A |
T |
15: 44,525,988 (GRCm38) |
I1380F |
probably damaging |
Het |
Plekha1 |
T |
C |
7: 130,892,253 (GRCm38) |
V106A |
probably benign |
Het |
Plekhm1 |
A |
T |
11: 103,376,691 (GRCm38) |
V818E |
possibly damaging |
Het |
Pprc1 |
T |
G |
19: 46,065,370 (GRCm38) |
|
probably benign |
Het |
Prmt9 |
T |
C |
8: 77,561,018 (GRCm38) |
|
probably benign |
Het |
Rab26 |
T |
C |
17: 24,530,399 (GRCm38) |
N193D |
possibly damaging |
Het |
Rnf111 |
A |
G |
9: 70,429,580 (GRCm38) |
S942P |
probably damaging |
Het |
Scgb2b18 |
T |
C |
7: 33,173,225 (GRCm38) |
T52A |
probably damaging |
Het |
Syt3 |
C |
T |
7: 44,392,763 (GRCm38) |
Q349* |
probably null |
Het |
Tas2r107 |
T |
C |
6: 131,659,780 (GRCm38) |
N102S |
probably benign |
Het |
Tas2r126 |
T |
A |
6: 42,435,000 (GRCm38) |
Y156N |
possibly damaging |
Het |
Tcaf2 |
A |
T |
6: 42,642,778 (GRCm38) |
I105N |
probably benign |
Het |
Tet1 |
A |
C |
10: 62,879,773 (GRCm38) |
M81R |
probably benign |
Het |
Togaram2 |
T |
C |
17: 71,729,205 (GRCm38) |
Y897H |
probably damaging |
Het |
Trerf1 |
A |
T |
17: 47,314,271 (GRCm38) |
|
noncoding transcript |
Het |
Ttn |
G |
A |
2: 76,761,235 (GRCm38) |
T12703I |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,125,626 (GRCm38) |
K1735E |
possibly damaging |
Het |
Usp54 |
G |
A |
14: 20,583,351 (GRCm38) |
T372I |
possibly damaging |
Het |
Wdr24 |
T |
C |
17: 25,827,128 (GRCm38) |
S476P |
probably benign |
Het |
Wdr78 |
G |
A |
4: 103,049,589 (GRCm38) |
P676S |
probably benign |
Het |
Zbtb1 |
T |
C |
12: 76,386,275 (GRCm38) |
I345T |
possibly damaging |
Het |
Zcrb1 |
T |
A |
15: 93,395,615 (GRCm38) |
I29L |
probably benign |
Het |
Zfp623 |
C |
A |
15: 75,948,163 (GRCm38) |
R323S |
probably benign |
Het |
Zfp831 |
T |
A |
2: 174,644,092 (GRCm38) |
Y187N |
possibly damaging |
Het |
|
Other mutations in Zfp341 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Zfp341
|
APN |
2 |
154,634,231 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01352:Zfp341
|
APN |
2 |
154,628,896 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01748:Zfp341
|
APN |
2 |
154,628,927 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02260:Zfp341
|
APN |
2 |
154,642,049 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL02329:Zfp341
|
APN |
2 |
154,632,304 (GRCm38) |
missense |
possibly damaging |
0.90 |
casanova_grimbacher
|
UTSW |
2 |
154,624,881 (GRCm38) |
missense |
probably damaging |
1.00 |
Specious
|
UTSW |
2 |
154,646,134 (GRCm38) |
missense |
possibly damaging |
0.63 |
R0079:Zfp341
|
UTSW |
2 |
154,624,994 (GRCm38) |
nonsense |
probably null |
|
R0570:Zfp341
|
UTSW |
2 |
154,646,068 (GRCm38) |
missense |
probably benign |
0.02 |
R0620:Zfp341
|
UTSW |
2 |
154,634,273 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1018:Zfp341
|
UTSW |
2 |
154,646,052 (GRCm38) |
missense |
probably damaging |
1.00 |
R1611:Zfp341
|
UTSW |
2 |
154,645,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R1733:Zfp341
|
UTSW |
2 |
154,641,378 (GRCm38) |
missense |
probably benign |
0.19 |
R1822:Zfp341
|
UTSW |
2 |
154,646,134 (GRCm38) |
missense |
possibly damaging |
0.63 |
R1956:Zfp341
|
UTSW |
2 |
154,638,212 (GRCm38) |
missense |
probably benign |
0.09 |
R2437:Zfp341
|
UTSW |
2 |
154,628,801 (GRCm38) |
missense |
probably damaging |
0.97 |
R3623:Zfp341
|
UTSW |
2 |
154,624,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R4417:Zfp341
|
UTSW |
2 |
154,628,987 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4806:Zfp341
|
UTSW |
2 |
154,645,866 (GRCm38) |
utr 3 prime |
probably benign |
|
R4807:Zfp341
|
UTSW |
2 |
154,645,866 (GRCm38) |
utr 3 prime |
probably benign |
|
R4863:Zfp341
|
UTSW |
2 |
154,645,866 (GRCm38) |
utr 3 prime |
probably benign |
|
R4955:Zfp341
|
UTSW |
2 |
154,638,030 (GRCm38) |
missense |
probably damaging |
0.98 |
R4962:Zfp341
|
UTSW |
2 |
154,626,814 (GRCm38) |
missense |
possibly damaging |
0.80 |
R5484:Zfp341
|
UTSW |
2 |
154,625,001 (GRCm38) |
missense |
probably benign |
0.00 |
R5864:Zfp341
|
UTSW |
2 |
154,643,554 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5877:Zfp341
|
UTSW |
2 |
154,632,289 (GRCm38) |
missense |
probably damaging |
1.00 |
R5990:Zfp341
|
UTSW |
2 |
154,645,659 (GRCm38) |
missense |
probably damaging |
0.98 |
R6057:Zfp341
|
UTSW |
2 |
154,625,034 (GRCm38) |
missense |
probably benign |
0.01 |
R6882:Zfp341
|
UTSW |
2 |
154,638,023 (GRCm38) |
missense |
probably damaging |
1.00 |
R7686:Zfp341
|
UTSW |
2 |
154,624,861 (GRCm38) |
missense |
probably damaging |
0.96 |
R7701:Zfp341
|
UTSW |
2 |
154,634,080 (GRCm38) |
splice site |
probably null |
|
R7847:Zfp341
|
UTSW |
2 |
154,634,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R8109:Zfp341
|
UTSW |
2 |
154,627,900 (GRCm38) |
missense |
probably benign |
0.04 |
R9313:Zfp341
|
UTSW |
2 |
154,627,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R9484:Zfp341
|
UTSW |
2 |
154,643,843 (GRCm38) |
missense |
probably damaging |
1.00 |
|