Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
C |
T |
17: 24,500,370 (GRCm39) |
V1274M |
probably damaging |
Het |
Abca4 |
A |
G |
3: 121,967,556 (GRCm39) |
H2202R |
possibly damaging |
Het |
Ablim3 |
A |
G |
18: 61,953,463 (GRCm39) |
L350P |
probably benign |
Het |
Adamts17 |
C |
T |
7: 66,654,117 (GRCm39) |
T449I |
probably damaging |
Het |
Ankrd39 |
T |
A |
1: 36,586,241 (GRCm39) |
D9V |
probably benign |
Het |
Arhgef7 |
T |
C |
8: 11,835,819 (GRCm39) |
V192A |
probably damaging |
Het |
Art4 |
C |
T |
6: 136,834,269 (GRCm39) |
|
probably benign |
Het |
Atg4a-ps |
A |
T |
3: 103,553,254 (GRCm39) |
V29E |
possibly damaging |
Het |
Ccdc180 |
A |
T |
4: 45,949,466 (GRCm39) |
K1574* |
probably null |
Het |
Cfap54 |
T |
G |
10: 92,846,882 (GRCm39) |
T1028P |
probably damaging |
Het |
Clip2 |
C |
T |
5: 134,532,254 (GRCm39) |
R517H |
possibly damaging |
Het |
Col5a1 |
A |
G |
2: 27,914,665 (GRCm39) |
T94A |
probably benign |
Het |
Cpne1 |
T |
A |
2: 155,918,210 (GRCm39) |
|
probably null |
Het |
Csnk2a1-ps3 |
A |
T |
1: 156,352,213 (GRCm39) |
Y138F |
probably benign |
Het |
Cyp2f2 |
T |
A |
7: 26,830,667 (GRCm39) |
M346K |
possibly damaging |
Het |
D130040H23Rik |
AAGAATATATTCTACAGAATATA |
AAGAATATA |
8: 69,755,748 (GRCm39) |
|
probably null |
Het |
Ddi2 |
T |
A |
4: 141,419,590 (GRCm39) |
I387F |
probably benign |
Het |
Dsg1b |
A |
G |
18: 20,523,282 (GRCm39) |
N103S |
probably damaging |
Het |
Duxf3 |
GCCC |
GCC |
10: 58,066,944 (GRCm39) |
|
probably null |
Het |
Dysf |
A |
G |
6: 84,156,666 (GRCm39) |
I1464V |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,044,012 (GRCm39) |
Y314C |
possibly damaging |
Het |
Etl4 |
A |
G |
2: 20,782,964 (GRCm39) |
E675G |
probably damaging |
Het |
Fam114a1 |
A |
C |
5: 65,188,733 (GRCm39) |
I488L |
probably benign |
Het |
Fbxo31 |
G |
A |
8: 122,281,136 (GRCm39) |
R337C |
probably damaging |
Het |
Fn1 |
A |
C |
1: 71,647,149 (GRCm39) |
I1547S |
probably null |
Het |
Garre1 |
A |
T |
7: 33,956,770 (GRCm39) |
|
probably null |
Het |
Get1 |
T |
A |
16: 95,954,244 (GRCm39) |
|
probably benign |
Het |
Gm14305 |
T |
A |
2: 176,413,045 (GRCm39) |
Y312* |
probably null |
Het |
Golm2 |
T |
A |
2: 121,756,096 (GRCm39) |
L375Q |
probably damaging |
Het |
Gpihbp1 |
A |
G |
15: 75,469,641 (GRCm39) |
T119A |
possibly damaging |
Het |
Harbi1 |
T |
G |
2: 91,542,980 (GRCm39) |
V147G |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,899 (GRCm39) |
Y186C |
probably damaging |
Het |
Ighv13-2 |
C |
A |
12: 114,321,494 (GRCm39) |
A82S |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,364,352 (GRCm39) |
D827E |
probably benign |
Het |
Krtap4-2 |
C |
T |
11: 99,525,801 (GRCm39) |
G17D |
unknown |
Het |
Ly6a |
A |
T |
15: 74,867,333 (GRCm39) |
|
probably benign |
Het |
Mad1l1 |
C |
T |
5: 140,288,741 (GRCm39) |
E203K |
probably damaging |
Het |
Mapk14 |
C |
A |
17: 28,934,413 (GRCm39) |
D101E |
probably benign |
Het |
Meis3 |
G |
T |
7: 15,917,764 (GRCm39) |
G306W |
probably damaging |
Het |
Mixl1 |
T |
C |
1: 180,524,402 (GRCm39) |
D59G |
probably benign |
Het |
Nav2 |
G |
A |
7: 49,254,293 (GRCm39) |
V2364M |
probably damaging |
Het |
Nell1 |
T |
C |
7: 50,506,150 (GRCm39) |
S786P |
possibly damaging |
Het |
Or13a25 |
T |
G |
7: 140,247,813 (GRCm39) |
N197K |
probably damaging |
Het |
Or51e2 |
C |
A |
7: 102,391,473 (GRCm39) |
V246L |
possibly damaging |
Het |
Or51g1 |
A |
G |
7: 102,633,687 (GRCm39) |
L228P |
probably damaging |
Het |
Or5b107 |
T |
G |
19: 13,143,310 (GRCm39) |
S311A |
probably benign |
Het |
Pcdhgb8 |
A |
T |
18: 37,896,052 (GRCm39) |
D374V |
probably damaging |
Het |
Phactr2 |
A |
G |
10: 13,129,386 (GRCm39) |
I294T |
probably benign |
Het |
Plekha4 |
C |
T |
7: 45,190,492 (GRCm39) |
A400V |
probably damaging |
Het |
Pramel21 |
T |
C |
4: 143,341,760 (GRCm39) |
F63S |
probably damaging |
Het |
Pramel4 |
C |
A |
4: 143,794,928 (GRCm39) |
D441E |
probably benign |
Het |
Prr12 |
G |
A |
7: 44,695,267 (GRCm39) |
P1400S |
unknown |
Het |
Prss3b |
T |
A |
6: 41,010,038 (GRCm39) |
N99Y |
possibly damaging |
Het |
Rbm6 |
G |
A |
9: 107,669,089 (GRCm39) |
Q608* |
probably null |
Het |
Scamp1 |
T |
A |
13: 94,369,598 (GRCm39) |
I76F |
probably benign |
Het |
Sez6 |
G |
A |
11: 77,865,121 (GRCm39) |
E623K |
possibly damaging |
Het |
Sirt1 |
A |
T |
10: 63,158,077 (GRCm39) |
S446T |
probably damaging |
Het |
Slc25a54 |
A |
G |
3: 109,019,404 (GRCm39) |
K336R |
probably benign |
Het |
Spag17 |
G |
T |
3: 99,912,092 (GRCm39) |
V321F |
possibly damaging |
Het |
Sstr1 |
A |
G |
12: 58,259,620 (GRCm39) |
Y81C |
probably damaging |
Het |
St8sia4 |
T |
C |
1: 95,519,525 (GRCm39) |
K321R |
probably damaging |
Het |
Stac3 |
T |
C |
10: 127,343,584 (GRCm39) |
F242S |
probably damaging |
Het |
Tanc2 |
T |
G |
11: 105,758,104 (GRCm39) |
S622A |
probably benign |
Het |
Tcf4 |
G |
A |
18: 69,598,464 (GRCm39) |
D106N |
possibly damaging |
Het |
Tfrc |
T |
A |
16: 32,433,571 (GRCm39) |
I75N |
possibly damaging |
Het |
Tigd2 |
G |
A |
6: 59,187,509 (GRCm39) |
W125* |
probably null |
Het |
Tjp1 |
T |
C |
7: 64,952,745 (GRCm39) |
T1530A |
possibly damaging |
Het |
Tmem132a |
T |
A |
19: 10,844,412 (GRCm39) |
H62L |
probably benign |
Het |
Tmem89 |
T |
C |
9: 108,743,729 (GRCm39) |
S10P |
unknown |
Het |
Trrap |
C |
T |
5: 144,733,961 (GRCm39) |
P938L |
probably damaging |
Het |
Unc80 |
C |
A |
1: 66,545,912 (GRCm39) |
P488T |
probably damaging |
Het |
Uri1 |
C |
A |
7: 37,662,873 (GRCm39) |
G374C |
probably damaging |
Het |
Utp20 |
T |
C |
10: 88,611,180 (GRCm39) |
N1379S |
probably damaging |
Het |
Vcan |
G |
T |
13: 89,852,644 (GRCm39) |
T772K |
probably benign |
Het |
Zbtb37 |
A |
T |
1: 160,847,941 (GRCm39) |
Y355* |
probably null |
Het |
Zfp629 |
A |
T |
7: 127,209,547 (GRCm39) |
L754Q |
probably damaging |
Het |
|
Other mutations in Zfp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0684:Zfp3
|
UTSW |
11 |
70,662,395 (GRCm39) |
missense |
probably benign |
0.09 |
R1067:Zfp3
|
UTSW |
11 |
70,663,411 (GRCm39) |
missense |
probably damaging |
0.97 |
R1389:Zfp3
|
UTSW |
11 |
70,663,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Zfp3
|
UTSW |
11 |
70,662,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1962:Zfp3
|
UTSW |
11 |
70,662,954 (GRCm39) |
nonsense |
probably null |
|
R4112:Zfp3
|
UTSW |
11 |
70,662,333 (GRCm39) |
missense |
probably benign |
0.14 |
R4637:Zfp3
|
UTSW |
11 |
70,662,181 (GRCm39) |
missense |
probably benign |
0.21 |
R6006:Zfp3
|
UTSW |
11 |
70,662,590 (GRCm39) |
missense |
probably benign |
0.00 |
R6333:Zfp3
|
UTSW |
11 |
70,662,266 (GRCm39) |
missense |
probably benign |
0.00 |
R7213:Zfp3
|
UTSW |
11 |
70,663,351 (GRCm39) |
missense |
probably benign |
0.24 |
R7378:Zfp3
|
UTSW |
11 |
70,662,899 (GRCm39) |
missense |
probably benign |
0.11 |
R8434:Zfp3
|
UTSW |
11 |
70,663,384 (GRCm39) |
missense |
probably benign |
0.08 |
R9094:Zfp3
|
UTSW |
11 |
70,663,241 (GRCm39) |
missense |
probably benign |
0.31 |
R9404:Zfp3
|
UTSW |
11 |
70,663,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R9622:Zfp3
|
UTSW |
11 |
70,662,739 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Zfp3
|
UTSW |
11 |
70,662,152 (GRCm39) |
missense |
probably benign |
|
Z1177:Zfp3
|
UTSW |
11 |
70,662,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|