Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
C |
A |
6: 121,636,262 (GRCm39) |
H710Q |
probably benign |
Het |
Abca14 |
A |
T |
7: 119,917,985 (GRCm39) |
K1496* |
probably null |
Het |
Anapc1 |
C |
A |
2: 128,476,613 (GRCm39) |
R1335L |
probably damaging |
Het |
Arhgef10l |
A |
T |
4: 140,305,605 (GRCm39) |
S203T |
probably benign |
Het |
Astn1 |
C |
T |
1: 158,491,674 (GRCm39) |
T41I |
possibly damaging |
Het |
Atrnl1 |
T |
A |
19: 57,743,949 (GRCm39) |
Y1184N |
possibly damaging |
Het |
Avil |
A |
G |
10: 126,849,513 (GRCm39) |
N603S |
probably benign |
Het |
Brca1 |
T |
C |
11: 101,421,916 (GRCm39) |
D149G |
possibly damaging |
Het |
Car14 |
C |
A |
3: 95,806,763 (GRCm39) |
A234S |
probably benign |
Het |
Cep164 |
A |
C |
9: 45,682,885 (GRCm39) |
L935R |
probably damaging |
Het |
Cps1 |
T |
C |
1: 67,268,577 (GRCm39) |
V1435A |
possibly damaging |
Het |
Csmd2 |
T |
G |
4: 128,438,536 (GRCm39) |
S3038R |
probably benign |
Het |
Cyp2j6 |
A |
T |
4: 96,406,394 (GRCm39) |
I459N |
probably damaging |
Het |
Cyth1 |
T |
C |
11: 118,073,132 (GRCm39) |
E242G |
probably damaging |
Het |
Dclk3 |
T |
G |
9: 111,296,738 (GRCm39) |
L94R |
possibly damaging |
Het |
Disp2 |
T |
C |
2: 118,622,297 (GRCm39) |
S1010P |
probably damaging |
Het |
Dlec1 |
G |
A |
9: 118,934,892 (GRCm39) |
R145H |
probably damaging |
Het |
Dsg3 |
T |
C |
18: 20,673,191 (GRCm39) |
V954A |
probably damaging |
Het |
Dync2h1 |
T |
A |
9: 7,111,487 (GRCm39) |
D309V |
probably damaging |
Het |
Fam13b |
A |
G |
18: 34,584,361 (GRCm39) |
I601T |
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,216 (GRCm39) |
M325K |
possibly damaging |
Het |
Frmpd1 |
A |
T |
4: 45,279,340 (GRCm39) |
E688D |
probably benign |
Het |
Gabrb1 |
C |
T |
5: 72,279,289 (GRCm39) |
|
probably benign |
Het |
Gm6590 |
A |
T |
6: 130,461,869 (GRCm39) |
|
noncoding transcript |
Het |
Gse1 |
T |
A |
8: 121,294,524 (GRCm39) |
S284T |
probably damaging |
Het |
Ipo13 |
C |
T |
4: 117,762,213 (GRCm39) |
R387Q |
possibly damaging |
Het |
Kctd16 |
A |
G |
18: 40,392,204 (GRCm39) |
E264G |
probably benign |
Het |
Krt73 |
A |
T |
15: 101,704,830 (GRCm39) |
L352* |
probably null |
Het |
Mapk15 |
A |
T |
15: 75,867,926 (GRCm39) |
K153* |
probably null |
Het |
Mcemp1 |
C |
A |
8: 3,717,055 (GRCm39) |
Y65* |
probably null |
Het |
Mcoln2 |
C |
G |
3: 145,881,473 (GRCm39) |
R210G |
probably damaging |
Het |
Miox |
G |
A |
15: 89,219,784 (GRCm39) |
V91I |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,453,594 (GRCm39) |
E6G |
possibly damaging |
Het |
Ncapg |
A |
G |
5: 45,851,090 (GRCm39) |
|
probably null |
Het |
Nfyb |
G |
A |
10: 82,590,836 (GRCm39) |
A65V |
possibly damaging |
Het |
Or4a69 |
A |
G |
2: 89,313,147 (GRCm39) |
F111L |
probably benign |
Het |
Or52d1 |
T |
C |
7: 103,755,812 (GRCm39) |
S109P |
probably damaging |
Het |
Or5b94 |
C |
A |
19: 12,652,224 (GRCm39) |
F218L |
probably benign |
Het |
Osbp2 |
A |
C |
11: 3,661,791 (GRCm39) |
S754A |
probably benign |
Het |
Pard3 |
C |
T |
8: 128,125,147 (GRCm39) |
R712C |
probably damaging |
Het |
Parp9 |
T |
C |
16: 35,768,711 (GRCm39) |
I64T |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,710,974 (GRCm39) |
H81Q |
possibly damaging |
Het |
Pcnt |
G |
A |
10: 76,225,030 (GRCm39) |
P1825S |
probably benign |
Het |
Pfkfb4 |
T |
C |
9: 108,827,957 (GRCm39) |
V43A |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,533,984 (GRCm39) |
V643E |
probably damaging |
Het |
Pip5k1a |
T |
C |
3: 94,972,753 (GRCm39) |
T433A |
probably benign |
Het |
Pip5k1b |
T |
A |
19: 24,356,411 (GRCm39) |
M176L |
probably benign |
Het |
Polg2 |
T |
C |
11: 106,667,958 (GRCm39) |
|
probably benign |
Het |
Pomp |
T |
A |
5: 147,812,323 (GRCm39) |
H136Q |
probably benign |
Het |
Ppfia4 |
A |
T |
1: 134,251,955 (GRCm39) |
|
probably null |
Het |
Prdx2 |
G |
A |
8: 85,696,880 (GRCm39) |
G4S |
probably benign |
Het |
Rbm28 |
C |
T |
6: 29,160,104 (GRCm39) |
G70D |
probably benign |
Het |
Rdh10 |
T |
A |
1: 16,176,489 (GRCm39) |
I83N |
probably damaging |
Het |
Rin3 |
A |
G |
12: 102,279,340 (GRCm39) |
I50V |
possibly damaging |
Het |
Rnf122 |
T |
C |
8: 31,614,877 (GRCm39) |
|
probably benign |
Het |
Sik2 |
A |
G |
9: 50,810,775 (GRCm39) |
M447T |
possibly damaging |
Het |
Sla2 |
A |
G |
2: 156,725,507 (GRCm39) |
|
probably null |
Het |
Slc51a |
T |
A |
16: 32,296,425 (GRCm39) |
I192L |
probably benign |
Het |
Sorcs1 |
T |
C |
19: 50,367,329 (GRCm39) |
|
probably benign |
Het |
Spata16 |
T |
A |
3: 26,967,416 (GRCm39) |
F389I |
probably damaging |
Het |
Srebf1 |
G |
A |
11: 60,092,630 (GRCm39) |
A793V |
probably benign |
Het |
Tbc1d9b |
T |
C |
11: 50,049,261 (GRCm39) |
V736A |
probably benign |
Het |
Tbx15 |
C |
A |
3: 99,259,182 (GRCm39) |
T351N |
possibly damaging |
Het |
Tep1 |
A |
G |
14: 51,089,373 (GRCm39) |
|
probably null |
Het |
Tmed11 |
T |
A |
5: 108,925,278 (GRCm39) |
D178V |
probably damaging |
Het |
Traf7 |
A |
G |
17: 24,732,900 (GRCm39) |
F110L |
probably benign |
Het |
Ubqlnl |
C |
T |
7: 103,799,399 (GRCm39) |
V33M |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,826,192 (GRCm39) |
|
probably null |
Het |
Vmn1r194 |
A |
G |
13: 22,429,217 (GRCm39) |
Y278C |
probably damaging |
Het |
Vmn1r46 |
T |
C |
6: 89,954,044 (GRCm39) |
F298L |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,572,265 (GRCm39) |
T961A |
probably benign |
Het |
Wdr48 |
G |
A |
9: 119,747,634 (GRCm39) |
|
probably benign |
Het |
Wwp1 |
G |
A |
4: 19,641,725 (GRCm39) |
|
probably benign |
Het |
Zfp1001 |
A |
T |
2: 150,165,761 (GRCm39) |
|
probably benign |
Het |
Zfp217 |
C |
T |
2: 169,957,382 (GRCm39) |
A539T |
probably benign |
Het |
|
Other mutations in Zfp839 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00821:Zfp839
|
APN |
12 |
110,831,441 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00941:Zfp839
|
APN |
12 |
110,827,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Zfp839
|
UTSW |
12 |
110,834,820 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0013:Zfp839
|
UTSW |
12 |
110,834,820 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0116:Zfp839
|
UTSW |
12 |
110,825,203 (GRCm39) |
intron |
probably benign |
|
R1219:Zfp839
|
UTSW |
12 |
110,834,707 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1406:Zfp839
|
UTSW |
12 |
110,832,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R1406:Zfp839
|
UTSW |
12 |
110,832,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R1434:Zfp839
|
UTSW |
12 |
110,827,333 (GRCm39) |
missense |
probably benign |
0.08 |
R1653:Zfp839
|
UTSW |
12 |
110,821,684 (GRCm39) |
missense |
probably benign |
0.02 |
R1754:Zfp839
|
UTSW |
12 |
110,821,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R2182:Zfp839
|
UTSW |
12 |
110,834,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R3765:Zfp839
|
UTSW |
12 |
110,821,597 (GRCm39) |
missense |
probably benign |
0.22 |
R3981:Zfp839
|
UTSW |
12 |
110,832,765 (GRCm39) |
missense |
probably damaging |
0.97 |
R4756:Zfp839
|
UTSW |
12 |
110,821,635 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5088:Zfp839
|
UTSW |
12 |
110,834,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R5394:Zfp839
|
UTSW |
12 |
110,822,020 (GRCm39) |
missense |
probably benign |
0.05 |
R5619:Zfp839
|
UTSW |
12 |
110,830,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Zfp839
|
UTSW |
12 |
110,833,195 (GRCm39) |
nonsense |
probably null |
|
R7661:Zfp839
|
UTSW |
12 |
110,835,226 (GRCm39) |
missense |
probably benign |
0.32 |
R7860:Zfp839
|
UTSW |
12 |
110,822,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Zfp839
|
UTSW |
12 |
110,821,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8855:Zfp839
|
UTSW |
12 |
110,834,848 (GRCm39) |
missense |
probably benign |
0.06 |
R8866:Zfp839
|
UTSW |
12 |
110,834,848 (GRCm39) |
missense |
probably benign |
0.06 |
R8896:Zfp839
|
UTSW |
12 |
110,835,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:Zfp839
|
UTSW |
12 |
110,834,878 (GRCm39) |
missense |
probably benign |
0.04 |
R9606:Zfp839
|
UTSW |
12 |
110,834,776 (GRCm39) |
missense |
probably benign |
|
R9668:Zfp839
|
UTSW |
12 |
110,822,280 (GRCm39) |
missense |
probably damaging |
0.98 |
R9686:Zfp839
|
UTSW |
12 |
110,821,932 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zfp839
|
UTSW |
12 |
110,833,218 (GRCm39) |
missense |
probably benign |
0.03 |
|