Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
T |
C |
11: 48,839,352 (GRCm39) |
T412A |
probably benign |
Het |
Aldh5a1 |
T |
A |
13: 25,097,776 (GRCm39) |
M420L |
possibly damaging |
Het |
Armc2 |
A |
G |
10: 41,884,711 (GRCm39) |
S77P |
probably damaging |
Het |
Avil |
A |
G |
10: 126,856,317 (GRCm39) |
|
probably null |
Het |
Bltp3a |
A |
G |
17: 28,100,530 (GRCm39) |
H323R |
probably damaging |
Het |
Bmp5 |
T |
A |
9: 75,801,035 (GRCm39) |
F388L |
probably damaging |
Het |
Brca2 |
T |
G |
5: 150,465,573 (GRCm39) |
V1779G |
possibly damaging |
Het |
Cblb |
T |
A |
16: 51,932,483 (GRCm39) |
S147T |
probably damaging |
Het |
Cblc |
T |
C |
7: 19,519,233 (GRCm39) |
E409G |
probably benign |
Het |
Cdc34b |
C |
T |
11: 94,632,886 (GRCm39) |
R29W |
probably damaging |
Het |
Clic6 |
T |
A |
16: 92,324,954 (GRCm39) |
Y371N |
probably benign |
Het |
Col5a2 |
A |
G |
1: 45,425,991 (GRCm39) |
|
probably null |
Het |
Coro1a |
A |
T |
7: 126,302,221 (GRCm39) |
V42D |
probably damaging |
Het |
Cpa3 |
C |
T |
3: 20,281,387 (GRCm39) |
C173Y |
probably damaging |
Het |
Crb1 |
A |
C |
1: 139,170,756 (GRCm39) |
V817G |
probably damaging |
Het |
Cyp2c39 |
A |
G |
19: 39,549,378 (GRCm39) |
T299A |
possibly damaging |
Het |
Dock5 |
G |
A |
14: 68,029,738 (GRCm39) |
R1019C |
probably benign |
Het |
Exoc8 |
T |
C |
8: 125,622,952 (GRCm39) |
T472A |
probably benign |
Het |
Fancc |
A |
G |
13: 63,469,679 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
T |
A |
7: 27,852,733 (GRCm39) |
M1340K |
probably benign |
Het |
Inpp5d |
T |
C |
1: 87,604,064 (GRCm39) |
L244P |
probably damaging |
Het |
Ireb2 |
A |
G |
9: 54,799,831 (GRCm39) |
N424S |
probably benign |
Het |
Krt35 |
T |
C |
11: 99,984,875 (GRCm39) |
D261G |
probably damaging |
Het |
Lipc |
T |
A |
9: 70,720,192 (GRCm39) |
I272L |
probably benign |
Het |
Lpcat3 |
A |
G |
6: 124,676,357 (GRCm39) |
|
probably benign |
Het |
Lzts1 |
T |
C |
8: 69,591,236 (GRCm39) |
D304G |
probably benign |
Het |
Mdn1 |
A |
G |
4: 32,774,008 (GRCm39) |
I5540V |
possibly damaging |
Het |
Msln |
T |
C |
17: 25,970,563 (GRCm39) |
S231G |
probably benign |
Het |
Mup8 |
G |
A |
4: 60,221,062 (GRCm39) |
T101M |
probably benign |
Het |
Myh8 |
T |
C |
11: 67,179,179 (GRCm39) |
I524T |
probably damaging |
Het |
Pappa2 |
A |
G |
1: 158,589,189 (GRCm39) |
C1679R |
probably damaging |
Het |
Pcdhb1 |
T |
C |
18: 37,399,416 (GRCm39) |
S456P |
possibly damaging |
Het |
Pcdhga5 |
A |
G |
18: 37,828,719 (GRCm39) |
N389S |
probably benign |
Het |
Pitrm1 |
C |
A |
13: 6,617,507 (GRCm39) |
S620R |
probably benign |
Het |
Plod3 |
T |
A |
5: 137,023,932 (GRCm39) |
|
probably benign |
Het |
Por |
A |
T |
5: 135,759,771 (GRCm39) |
Q194L |
probably benign |
Het |
Prkag3 |
A |
T |
1: 74,780,646 (GRCm39) |
Y396N |
probably damaging |
Het |
R3hcc1 |
T |
C |
14: 69,935,053 (GRCm39) |
|
probably null |
Het |
Rcan3 |
C |
T |
4: 135,152,592 (GRCm39) |
S43N |
probably damaging |
Het |
Rhot1 |
A |
G |
11: 80,111,098 (GRCm39) |
T31A |
probably damaging |
Het |
Rnps1 |
T |
G |
17: 24,637,486 (GRCm39) |
S43A |
unknown |
Het |
Rp1 |
T |
C |
1: 4,416,426 (GRCm39) |
D1562G |
possibly damaging |
Het |
Rps19-ps13 |
A |
G |
18: 40,859,428 (GRCm39) |
|
noncoding transcript |
Het |
Serpina3c |
A |
T |
12: 104,115,771 (GRCm39) |
S258T |
possibly damaging |
Het |
Smc2 |
G |
A |
4: 52,460,181 (GRCm39) |
R519Q |
possibly damaging |
Het |
Sorbs2 |
A |
T |
8: 46,248,767 (GRCm39) |
T593S |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,787,885 (GRCm39) |
T955A |
probably benign |
Het |
Stfa3 |
T |
C |
16: 36,272,581 (GRCm39) |
K40E |
probably damaging |
Het |
Tmem87b |
A |
G |
2: 128,666,378 (GRCm39) |
E75G |
probably benign |
Het |
Tmprss15 |
T |
C |
16: 78,800,298 (GRCm39) |
Q595R |
probably benign |
Het |
Trak1 |
A |
T |
9: 121,289,478 (GRCm39) |
I597F |
probably damaging |
Het |
Trat1 |
T |
C |
16: 48,555,300 (GRCm39) |
D144G |
probably damaging |
Het |
Trim25 |
T |
C |
11: 88,890,358 (GRCm39) |
V15A |
probably benign |
Het |
Tulp1 |
A |
C |
17: 28,578,034 (GRCm39) |
|
probably null |
Het |
Txndc15 |
T |
A |
13: 55,865,734 (GRCm39) |
M66K |
probably benign |
Het |
Vmn1r206 |
T |
A |
13: 22,804,775 (GRCm39) |
N144I |
probably damaging |
Het |
Wwc2 |
T |
C |
8: 48,353,796 (GRCm39) |
T113A |
probably benign |
Het |
Xpo5 |
A |
C |
17: 46,528,535 (GRCm39) |
E313D |
probably damaging |
Het |
|
Other mutations in Zfp790 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Zfp790
|
APN |
7 |
29,527,988 (GRCm39) |
missense |
probably benign |
0.32 |
IGL00979:Zfp790
|
APN |
7 |
29,529,034 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02286:Zfp790
|
APN |
7 |
29,529,160 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03136:Zfp790
|
APN |
7 |
29,529,320 (GRCm39) |
nonsense |
probably null |
|
R0021:Zfp790
|
UTSW |
7 |
29,525,113 (GRCm39) |
unclassified |
probably benign |
|
R0077:Zfp790
|
UTSW |
7 |
29,524,300 (GRCm39) |
missense |
probably damaging |
0.98 |
R1477:Zfp790
|
UTSW |
7 |
29,522,525 (GRCm39) |
start gained |
probably benign |
|
R1572:Zfp790
|
UTSW |
7 |
29,527,564 (GRCm39) |
missense |
probably benign |
0.33 |
R2015:Zfp790
|
UTSW |
7 |
29,528,286 (GRCm39) |
missense |
probably benign |
0.29 |
R4941:Zfp790
|
UTSW |
7 |
29,528,916 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5019:Zfp790
|
UTSW |
7 |
29,529,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5160:Zfp790
|
UTSW |
7 |
29,529,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5722:Zfp790
|
UTSW |
7 |
29,529,514 (GRCm39) |
nonsense |
probably null |
|
R5954:Zfp790
|
UTSW |
7 |
29,528,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Zfp790
|
UTSW |
7 |
29,528,970 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6312:Zfp790
|
UTSW |
7 |
29,527,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Zfp790
|
UTSW |
7 |
29,528,050 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7623:Zfp790
|
UTSW |
7 |
29,525,130 (GRCm39) |
nonsense |
probably null |
|
R8036:Zfp790
|
UTSW |
7 |
29,528,346 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8175:Zfp790
|
UTSW |
7 |
29,529,205 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8898:Zfp790
|
UTSW |
7 |
29,522,525 (GRCm39) |
start gained |
probably benign |
|
R8988:Zfp790
|
UTSW |
7 |
29,527,593 (GRCm39) |
missense |
probably benign |
|
R9176:Zfp790
|
UTSW |
7 |
29,529,387 (GRCm39) |
missense |
probably benign |
0.04 |
R9404:Zfp790
|
UTSW |
7 |
29,525,185 (GRCm39) |
missense |
probably benign |
|
R9519:Zfp790
|
UTSW |
7 |
29,522,567 (GRCm39) |
missense |
unknown |
|
Z1186:Zfp790
|
UTSW |
7 |
29,529,109 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1186:Zfp790
|
UTSW |
7 |
29,529,258 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1186:Zfp790
|
UTSW |
7 |
29,529,208 (GRCm39) |
missense |
possibly damaging |
0.72 |
|