Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago2 |
G |
A |
15: 72,993,089 (GRCm39) |
T472I |
possibly damaging |
Het |
Ambp |
T |
A |
4: 63,072,298 (GRCm39) |
|
probably benign |
Het |
As3mt |
T |
A |
19: 46,708,788 (GRCm39) |
F261I |
probably damaging |
Het |
Atxn1l |
A |
G |
8: 110,458,579 (GRCm39) |
L561P |
probably damaging |
Het |
Cnr2 |
A |
G |
4: 135,644,263 (GRCm39) |
T114A |
probably damaging |
Het |
Dchs1 |
A |
G |
7: 105,408,178 (GRCm39) |
Y1885H |
probably damaging |
Het |
Dcn |
A |
G |
10: 97,343,604 (GRCm39) |
N188S |
probably benign |
Het |
Dennd6b |
A |
C |
15: 89,070,955 (GRCm39) |
|
probably null |
Het |
Dstyk |
A |
G |
1: 132,377,665 (GRCm39) |
T424A |
probably benign |
Het |
Gabrr3 |
A |
G |
16: 59,250,298 (GRCm39) |
|
probably null |
Het |
Gnai3 |
A |
G |
3: 108,025,621 (GRCm39) |
S153P |
probably benign |
Het |
Igkv2-112 |
T |
A |
6: 68,197,599 (GRCm39) |
S90R |
probably damaging |
Het |
Lxn |
T |
C |
3: 67,365,979 (GRCm39) |
D173G |
probably damaging |
Het |
Mcm3ap |
T |
A |
10: 76,342,307 (GRCm39) |
I1600N |
probably damaging |
Het |
Myof |
A |
T |
19: 37,971,406 (GRCm39) |
|
probably null |
Het |
Nrxn1 |
T |
C |
17: 90,762,931 (GRCm39) |
|
probably benign |
Het |
Oaz3 |
A |
G |
3: 94,340,852 (GRCm39) |
Y232H |
unknown |
Het |
Or5aq1b |
A |
T |
2: 86,902,046 (GRCm39) |
M144K |
possibly damaging |
Het |
Pkdcc |
C |
T |
17: 83,527,577 (GRCm39) |
R252* |
probably null |
Het |
Plcl1 |
A |
G |
1: 55,741,090 (GRCm39) |
N907S |
probably benign |
Het |
Plscr1 |
T |
A |
9: 92,145,150 (GRCm39) |
Y53* |
probably null |
Het |
Pm20d2 |
T |
C |
4: 33,174,756 (GRCm39) |
T377A |
probably benign |
Het |
Ptchd3 |
T |
A |
11: 121,722,875 (GRCm39) |
V321D |
probably damaging |
Het |
Ranbp3l |
T |
C |
15: 9,060,829 (GRCm39) |
I366T |
probably damaging |
Het |
Sardh |
T |
C |
2: 27,087,660 (GRCm39) |
E737G |
probably damaging |
Het |
Scart2 |
T |
C |
7: 139,853,975 (GRCm39) |
F326S |
possibly damaging |
Het |
Scn1a |
T |
C |
2: 66,103,626 (GRCm39) |
E1878G |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,552,072 (GRCm39) |
V872A |
possibly damaging |
Het |
Sugp2 |
C |
T |
8: 70,713,195 (GRCm39) |
Q1054* |
probably null |
Het |
Syne3 |
T |
C |
12: 104,929,438 (GRCm39) |
T261A |
probably benign |
Het |
Tgif2 |
T |
C |
2: 156,695,232 (GRCm39) |
S126P |
probably benign |
Het |
Ticrr |
T |
C |
7: 79,319,386 (GRCm39) |
V457A |
possibly damaging |
Het |
Tm7sf2 |
T |
C |
19: 6,113,635 (GRCm39) |
I299V |
probably benign |
Het |
Tnks1bp1 |
A |
G |
2: 84,892,902 (GRCm39) |
E943G |
probably benign |
Het |
Tpd52l2 |
T |
A |
2: 181,141,681 (GRCm39) |
F21L |
probably benign |
Het |
Tpm2 |
A |
G |
4: 43,519,263 (GRCm39) |
L176P |
probably benign |
Het |
Trim34a |
C |
A |
7: 103,909,691 (GRCm39) |
T293K |
probably benign |
Het |
Ttc23 |
A |
T |
7: 67,312,135 (GRCm39) |
D14V |
probably damaging |
Het |
Twsg1 |
T |
C |
17: 66,236,706 (GRCm39) |
E108G |
probably benign |
Het |
Txndc15 |
C |
T |
13: 55,869,507 (GRCm39) |
A220V |
probably benign |
Het |
Vmn1r183 |
A |
G |
7: 23,754,266 (GRCm39) |
Q23R |
probably damaging |
Het |
Vmn1r31 |
A |
G |
6: 58,449,028 (GRCm39) |
V279A |
probably damaging |
Het |
Vmo1 |
A |
C |
11: 70,404,661 (GRCm39) |
C113W |
probably damaging |
Het |
Zik1 |
A |
C |
7: 10,226,256 (GRCm39) |
L37R |
probably benign |
Het |
|
Other mutations in Zfp984 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00469:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00550:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
R0281:Zfp984
|
UTSW |
4 |
147,839,722 (GRCm39) |
missense |
probably benign |
|
R0731:Zfp984
|
UTSW |
4 |
147,840,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Zfp984
|
UTSW |
4 |
147,840,446 (GRCm39) |
missense |
probably benign |
0.24 |
R1293:Zfp984
|
UTSW |
4 |
147,840,398 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1518:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
R2041:Zfp984
|
UTSW |
4 |
147,839,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R2360:Zfp984
|
UTSW |
4 |
147,839,234 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5038:Zfp984
|
UTSW |
4 |
147,839,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Zfp984
|
UTSW |
4 |
147,840,362 (GRCm39) |
missense |
probably benign |
0.00 |
R6254:Zfp984
|
UTSW |
4 |
147,840,643 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6418:Zfp984
|
UTSW |
4 |
147,845,703 (GRCm39) |
missense |
probably benign |
0.00 |
R6527:Zfp984
|
UTSW |
4 |
147,840,381 (GRCm39) |
missense |
probably benign |
0.45 |
R6974:Zfp984
|
UTSW |
4 |
147,845,707 (GRCm39) |
start codon destroyed |
possibly damaging |
0.94 |
R7058:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
R7495:Zfp984
|
UTSW |
4 |
147,839,287 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7843:Zfp984
|
UTSW |
4 |
147,842,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8462:Zfp984
|
UTSW |
4 |
147,839,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8520:Zfp984
|
UTSW |
4 |
147,840,668 (GRCm39) |
missense |
probably benign |
0.01 |
R8918:Zfp984
|
UTSW |
4 |
147,840,623 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9387:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
Z1176:Zfp984
|
UTSW |
4 |
147,839,921 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfp984
|
UTSW |
4 |
147,840,577 (GRCm39) |
missense |
probably benign |
0.04 |
|