Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afdn |
T |
A |
17: 14,024,270 (GRCm39) |
C59S |
probably damaging |
Het |
Aicda |
C |
T |
6: 122,538,854 (GRCm39) |
A161V |
possibly damaging |
Het |
Ankrd12 |
C |
T |
17: 66,344,599 (GRCm39) |
E91K |
possibly damaging |
Het |
Arpc2 |
C |
A |
1: 74,276,041 (GRCm39) |
F19L |
probably benign |
Het |
Aspa |
T |
C |
11: 73,215,280 (GRCm39) |
K12E |
possibly damaging |
Het |
Chd8 |
G |
A |
14: 52,472,627 (GRCm39) |
P392L |
probably benign |
Het |
Cldn10 |
C |
T |
14: 119,111,647 (GRCm39) |
R206W |
probably damaging |
Het |
Clec4b2 |
T |
A |
6: 123,181,224 (GRCm39) |
M203K |
probably damaging |
Het |
Clec4d |
G |
T |
6: 123,251,651 (GRCm39) |
E178* |
probably null |
Het |
Clec4d |
T |
C |
6: 123,251,649 (GRCm39) |
M177T |
probably benign |
Het |
Cmpk2 |
A |
T |
12: 26,519,568 (GRCm39) |
Y73F |
probably benign |
Het |
Col1a1 |
T |
A |
11: 94,838,103 (GRCm39) |
V845D |
unknown |
Het |
Cyp2c67 |
C |
T |
19: 39,597,699 (GRCm39) |
R433Q |
probably damaging |
Het |
Dda1 |
A |
T |
8: 71,927,130 (GRCm39) |
|
probably null |
Het |
Ddx60 |
A |
T |
8: 62,431,012 (GRCm39) |
Y849F |
possibly damaging |
Het |
Dnm2 |
C |
T |
9: 21,416,977 (GRCm39) |
R837W |
possibly damaging |
Het |
Dtwd1 |
C |
T |
2: 126,006,728 (GRCm39) |
T250I |
probably damaging |
Het |
Efcab6 |
A |
G |
15: 83,777,094 (GRCm39) |
V1114A |
probably damaging |
Het |
Fat4 |
A |
G |
3: 38,945,171 (GRCm39) |
T1355A |
probably benign |
Het |
Fbxo40 |
T |
G |
16: 36,789,940 (GRCm39) |
D390A |
possibly damaging |
Het |
Gnaz |
T |
A |
10: 74,827,437 (GRCm39) |
L63Q |
probably benign |
Het |
H6pd |
T |
A |
4: 150,080,307 (GRCm39) |
K179N |
probably damaging |
Het |
Hmgb2 |
A |
G |
8: 57,965,786 (GRCm39) |
|
probably benign |
Het |
Hps5 |
A |
G |
7: 46,440,397 (GRCm39) |
F18L |
probably benign |
Het |
Hyal5 |
A |
G |
6: 24,876,694 (GRCm39) |
E189G |
probably benign |
Het |
Ifnar1 |
T |
A |
16: 91,302,013 (GRCm39) |
I496N |
probably damaging |
Het |
Ift70a2 |
T |
C |
2: 75,807,375 (GRCm39) |
D379G |
probably damaging |
Het |
Igf2r |
C |
A |
17: 12,914,240 (GRCm39) |
C1743F |
probably damaging |
Het |
Igfn1 |
C |
A |
1: 135,901,185 (GRCm39) |
R431L |
probably damaging |
Het |
Itch |
A |
G |
2: 155,045,217 (GRCm39) |
Q507R |
probably benign |
Het |
Kbtbd2 |
C |
A |
6: 56,757,331 (GRCm39) |
R135L |
probably damaging |
Het |
Kcnn2 |
T |
C |
18: 45,725,446 (GRCm39) |
I314T |
probably damaging |
Het |
Lix1 |
A |
G |
17: 17,623,211 (GRCm39) |
D2G |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,487,076 (GRCm39) |
Y4557C |
|
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mcam |
G |
T |
9: 44,046,473 (GRCm39) |
|
probably benign |
Het |
Med19 |
G |
T |
2: 84,508,975 (GRCm39) |
G63C |
probably damaging |
Het |
Mfsd4b1 |
C |
T |
10: 39,883,330 (GRCm39) |
R40H |
probably damaging |
Het |
Neb |
C |
T |
2: 52,146,190 (GRCm39) |
R2929H |
probably damaging |
Het |
Nlrc5 |
A |
G |
8: 95,237,908 (GRCm39) |
D1434G |
probably benign |
Het |
Nlrp14 |
A |
T |
7: 106,797,049 (GRCm39) |
N972I |
probably damaging |
Het |
Or13a18 |
T |
C |
7: 140,190,936 (GRCm39) |
Y278H |
probably damaging |
Het |
Or14j7 |
A |
T |
17: 38,235,275 (GRCm39) |
M273L |
probably benign |
Het |
Or2h15 |
A |
T |
17: 38,441,693 (GRCm39) |
L130Q |
probably damaging |
Het |
Or4a74 |
A |
C |
2: 89,439,948 (GRCm39) |
F166C |
probably damaging |
Het |
Or8g29-ps1 |
A |
G |
9: 39,200,781 (GRCm39) |
V135A |
probably benign |
Het |
Otop1 |
T |
C |
5: 38,460,158 (GRCm39) |
V575A |
probably damaging |
Het |
Pcdhb4 |
A |
G |
18: 37,441,925 (GRCm39) |
S412G |
possibly damaging |
Het |
Pcsk4 |
T |
C |
10: 80,161,224 (GRCm39) |
D230G |
probably damaging |
Het |
Phldb2 |
C |
A |
16: 45,646,308 (GRCm39) |
S46I |
probably damaging |
Het |
Pik3ca |
A |
T |
3: 32,508,587 (GRCm39) |
N785I |
probably damaging |
Het |
Polr2b |
A |
G |
5: 77,471,485 (GRCm39) |
R274G |
probably damaging |
Het |
Prkdc |
G |
A |
16: 15,634,523 (GRCm39) |
|
probably null |
Het |
Prune2 |
C |
T |
19: 17,101,144 (GRCm39) |
T2216I |
probably benign |
Het |
Psma3 |
A |
T |
12: 71,041,156 (GRCm39) |
D252V |
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,326,768 (GRCm39) |
V1586A |
|
Het |
Ryr2 |
T |
C |
13: 11,897,976 (GRCm39) |
T140A |
probably benign |
Het |
Slc25a48 |
A |
G |
13: 56,611,552 (GRCm39) |
I220V |
probably benign |
Het |
Slc2a1 |
A |
T |
4: 118,990,607 (GRCm39) |
E246D |
probably benign |
Het |
Slc45a4 |
A |
G |
15: 73,458,206 (GRCm39) |
Y448H |
probably benign |
Het |
Sorl1 |
C |
T |
9: 41,957,857 (GRCm39) |
V596I |
probably benign |
Het |
Spag6 |
A |
C |
2: 18,703,985 (GRCm39) |
E11A |
probably benign |
Het |
Spef2 |
A |
G |
15: 9,727,495 (GRCm39) |
|
probably null |
Het |
Spon1 |
T |
C |
7: 113,628,188 (GRCm39) |
S315P |
probably damaging |
Het |
Stard3 |
G |
A |
11: 98,262,931 (GRCm39) |
|
probably benign |
Het |
Sv2c |
A |
G |
13: 96,112,589 (GRCm39) |
M636T |
probably damaging |
Het |
Syt17 |
T |
A |
7: 118,033,480 (GRCm39) |
D172V |
probably damaging |
Het |
Tcf4 |
A |
G |
18: 69,766,652 (GRCm39) |
Y206C |
probably damaging |
Het |
Tead2 |
G |
T |
7: 44,880,776 (GRCm39) |
S318I |
probably benign |
Het |
Tom1 |
A |
T |
8: 75,783,883 (GRCm39) |
D289V |
probably damaging |
Het |
Tonsl |
A |
G |
15: 76,520,971 (GRCm39) |
|
probably benign |
Het |
Tsen15 |
T |
C |
1: 152,259,098 (GRCm39) |
I87V |
probably damaging |
Het |
Usp15 |
A |
G |
10: 123,007,112 (GRCm39) |
F123S |
probably damaging |
Het |
Vmn1r220 |
A |
T |
13: 23,368,258 (GRCm39) |
I146N |
possibly damaging |
Het |
Vmn2r108 |
A |
T |
17: 20,692,561 (GRCm39) |
N98K |
probably benign |
Het |
Vmn2r71 |
T |
A |
7: 85,269,788 (GRCm39) |
M433K |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,134,762 (GRCm39) |
H60L |
probably benign |
Het |
Wbp4 |
A |
G |
14: 79,699,486 (GRCm39) |
V336A |
probably benign |
Het |
Zpld2 |
A |
G |
4: 133,922,770 (GRCm39) |
L521P |
probably damaging |
Het |
|
Other mutations in Zfp663 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00720:Zfp663
|
APN |
2 |
165,194,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01382:Zfp663
|
APN |
2 |
165,200,935 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02007:Zfp663
|
APN |
2 |
165,200,993 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02164:Zfp663
|
APN |
2 |
165,200,968 (GRCm39) |
nonsense |
probably null |
|
IGL02506:Zfp663
|
APN |
2 |
165,195,871 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03173:Zfp663
|
APN |
2 |
165,194,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R0735:Zfp663
|
UTSW |
2 |
165,200,995 (GRCm39) |
missense |
probably damaging |
0.97 |
R1395:Zfp663
|
UTSW |
2 |
165,194,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1402:Zfp663
|
UTSW |
2 |
165,195,890 (GRCm39) |
missense |
probably benign |
0.14 |
R1402:Zfp663
|
UTSW |
2 |
165,195,890 (GRCm39) |
missense |
probably benign |
0.14 |
R1503:Zfp663
|
UTSW |
2 |
165,194,573 (GRCm39) |
missense |
probably damaging |
0.99 |
R1587:Zfp663
|
UTSW |
2 |
165,195,437 (GRCm39) |
missense |
probably benign |
|
R1854:Zfp663
|
UTSW |
2 |
165,195,211 (GRCm39) |
missense |
probably benign |
0.18 |
R1867:Zfp663
|
UTSW |
2 |
165,194,651 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3031:Zfp663
|
UTSW |
2 |
165,195,616 (GRCm39) |
nonsense |
probably null |
|
R4643:Zfp663
|
UTSW |
2 |
165,194,925 (GRCm39) |
missense |
probably benign |
0.24 |
R4691:Zfp663
|
UTSW |
2 |
165,201,050 (GRCm39) |
intron |
probably benign |
|
R4977:Zfp663
|
UTSW |
2 |
165,195,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R5135:Zfp663
|
UTSW |
2 |
165,195,590 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5151:Zfp663
|
UTSW |
2 |
165,195,113 (GRCm39) |
missense |
probably benign |
0.00 |
R5639:Zfp663
|
UTSW |
2 |
165,194,929 (GRCm39) |
missense |
probably benign |
0.03 |
R5763:Zfp663
|
UTSW |
2 |
165,200,355 (GRCm39) |
nonsense |
probably null |
|
R6776:Zfp663
|
UTSW |
2 |
165,200,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R6929:Zfp663
|
UTSW |
2 |
165,195,178 (GRCm39) |
missense |
probably benign |
|
R6998:Zfp663
|
UTSW |
2 |
165,195,922 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7035:Zfp663
|
UTSW |
2 |
165,195,023 (GRCm39) |
missense |
probably benign |
0.36 |
R7169:Zfp663
|
UTSW |
2 |
165,194,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7529:Zfp663
|
UTSW |
2 |
165,194,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Zfp663
|
UTSW |
2 |
165,194,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R8087:Zfp663
|
UTSW |
2 |
165,195,679 (GRCm39) |
missense |
probably benign |
0.20 |
R8715:Zfp663
|
UTSW |
2 |
165,194,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R8934:Zfp663
|
UTSW |
2 |
165,194,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Zfp663
|
UTSW |
2 |
165,194,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R9257:Zfp663
|
UTSW |
2 |
165,195,974 (GRCm39) |
missense |
probably benign |
0.00 |
R9524:Zfp663
|
UTSW |
2 |
165,195,607 (GRCm39) |
missense |
probably damaging |
0.99 |
RF004:Zfp663
|
UTSW |
2 |
165,200,363 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfp663
|
UTSW |
2 |
165,195,033 (GRCm39) |
missense |
probably damaging |
0.99 |
|