Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
C |
A |
6: 121,631,571 (GRCm39) |
L623M |
probably benign |
Het |
Abhd2 |
T |
C |
7: 78,998,104 (GRCm39) |
I212T |
possibly damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aox3 |
T |
C |
1: 58,219,810 (GRCm39) |
Y1137H |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,888,474 (GRCm39) |
Y715H |
probably damaging |
Het |
Atrn |
A |
G |
2: 130,836,971 (GRCm39) |
Y1145C |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,760,055 (GRCm39) |
I631T |
probably benign |
Het |
Cadps |
T |
C |
14: 12,465,859 (GRCm38) |
K1017R |
possibly damaging |
Het |
Cfap45 |
A |
G |
1: 172,372,679 (GRCm39) |
E458G |
probably damaging |
Het |
Cptp |
C |
T |
4: 155,950,995 (GRCm39) |
R157H |
probably damaging |
Het |
Dcbld1 |
A |
C |
10: 52,195,747 (GRCm39) |
E318D |
possibly damaging |
Het |
Ddr2 |
G |
T |
1: 169,831,814 (GRCm39) |
P197Q |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,226,639 (GRCm39) |
Y421C |
probably damaging |
Het |
Dlgap2 |
A |
G |
8: 14,893,624 (GRCm39) |
K980E |
probably benign |
Het |
Drc7 |
T |
C |
8: 95,782,644 (GRCm39) |
V3A |
unknown |
Het |
Dst |
T |
C |
1: 34,200,110 (GRCm39) |
V96A |
probably damaging |
Het |
Ect2l |
T |
C |
10: 18,018,752 (GRCm39) |
D548G |
possibly damaging |
Het |
Efcab10 |
A |
T |
12: 33,448,434 (GRCm39) |
Y89F |
probably benign |
Het |
Eif1ad |
CGAGGAGGAGGAGGAGGAGG |
CGAGGAGGAGGAGGAGG |
19: 5,420,086 (GRCm39) |
|
probably benign |
Het |
Entpd6 |
A |
G |
2: 150,600,732 (GRCm39) |
T147A |
probably damaging |
Het |
Fbxl5 |
T |
A |
5: 43,922,832 (GRCm39) |
E189D |
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,497,080 (GRCm39) |
S1217T |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,560,916 (GRCm39) |
V1197D |
possibly damaging |
Het |
Fsip2 |
T |
A |
2: 82,811,127 (GRCm39) |
L2482* |
probably null |
Het |
Fsip2 |
A |
T |
2: 82,817,164 (GRCm39) |
D4299V |
probably benign |
Het |
Gipc3 |
T |
A |
10: 81,174,049 (GRCm39) |
I242F |
probably damaging |
Het |
Hoxb1 |
T |
A |
11: 96,256,938 (GRCm39) |
Y96N |
probably damaging |
Het |
Ibsp |
A |
G |
5: 104,458,078 (GRCm39) |
E205G |
probably damaging |
Het |
Ibtk |
A |
G |
9: 85,585,135 (GRCm39) |
S1170P |
probably benign |
Het |
Igfn1 |
A |
G |
1: 135,893,801 (GRCm39) |
|
probably null |
Het |
Iqsec1 |
A |
G |
6: 90,639,877 (GRCm39) |
S954P |
probably benign |
Het |
Kalrn |
A |
T |
16: 34,212,463 (GRCm39) |
D28E |
probably benign |
Het |
Lrmda |
T |
C |
14: 22,627,938 (GRCm39) |
F52L |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,353,631 (GRCm39) |
D543G |
probably damaging |
Het |
Lrrtm3 |
T |
C |
10: 63,924,157 (GRCm39) |
T337A |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,946,465 (GRCm39) |
D1219N |
possibly damaging |
Het |
Mkln1 |
A |
G |
6: 31,405,113 (GRCm39) |
K118R |
probably benign |
Het |
Nedd4l |
T |
C |
18: 65,300,646 (GRCm39) |
|
probably null |
Het |
Neu2 |
A |
G |
1: 87,525,023 (GRCm39) |
E336G |
probably benign |
Het |
Nfasc |
A |
G |
1: 132,538,543 (GRCm39) |
F448S |
probably damaging |
Het |
Nlrx1 |
C |
A |
9: 44,165,431 (GRCm39) |
E822* |
probably null |
Het |
Nr5a1 |
T |
C |
2: 38,584,108 (GRCm39) |
Y437C |
probably damaging |
Het |
Or4c119 |
A |
G |
2: 88,986,925 (GRCm39) |
V198A |
probably benign |
Het |
Or7a37 |
T |
A |
10: 78,805,975 (GRCm39) |
L164* |
probably null |
Het |
Or8b38 |
T |
C |
9: 37,972,981 (GRCm39) |
Y122H |
probably damaging |
Het |
Phtf1 |
C |
T |
3: 103,876,438 (GRCm39) |
Q13* |
probably null |
Het |
Pnldc1 |
A |
G |
17: 13,107,815 (GRCm39) |
L525P |
possibly damaging |
Het |
Ppl |
T |
A |
16: 4,923,988 (GRCm39) |
D162V |
possibly damaging |
Het |
Prkdc |
T |
A |
16: 15,532,079 (GRCm39) |
S1448T |
possibly damaging |
Het |
Ptgdr |
A |
G |
14: 45,090,738 (GRCm39) |
I340T |
probably benign |
Het |
Recql |
T |
C |
6: 142,311,315 (GRCm39) |
I458M |
probably benign |
Het |
Rrbp1 |
A |
T |
2: 143,830,211 (GRCm39) |
V652E |
probably benign |
Het |
Rtp1 |
T |
A |
16: 23,250,160 (GRCm39) |
I175N |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,754,369 (GRCm39) |
M3523T |
probably damaging |
Het |
S100a16 |
T |
C |
3: 90,449,703 (GRCm39) |
L62P |
probably damaging |
Het |
Samd11 |
T |
C |
4: 156,333,166 (GRCm39) |
E364G |
probably damaging |
Het |
Satb1 |
C |
A |
17: 52,049,143 (GRCm39) |
G603* |
probably null |
Het |
Shroom3 |
T |
A |
5: 93,110,224 (GRCm39) |
|
probably null |
Het |
Slc25a15 |
A |
G |
8: 22,885,777 (GRCm39) |
S3P |
probably benign |
Het |
Socs2 |
A |
T |
10: 95,248,900 (GRCm39) |
L71* |
probably null |
Het |
Sptbn1 |
T |
C |
11: 30,054,469 (GRCm39) |
E2208G |
probably damaging |
Het |
St14 |
A |
G |
9: 31,001,166 (GRCm39) |
V855A |
possibly damaging |
Het |
Susd1 |
T |
A |
4: 59,412,191 (GRCm39) |
T121S |
probably benign |
Het |
Svs3b |
A |
T |
2: 164,097,848 (GRCm39) |
S158T |
probably benign |
Het |
Synpo |
C |
T |
18: 60,736,661 (GRCm39) |
M428I |
probably benign |
Het |
Syt10 |
C |
T |
15: 89,674,979 (GRCm39) |
D456N |
probably damaging |
Het |
Taar4 |
A |
G |
10: 23,837,239 (GRCm39) |
D283G |
probably damaging |
Het |
Tango6 |
T |
A |
8: 107,415,426 (GRCm39) |
D82E |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,971,927 (GRCm39) |
T127A |
possibly damaging |
Het |
Tle3 |
G |
A |
9: 61,318,622 (GRCm39) |
|
probably null |
Het |
Tmem45a |
A |
G |
16: 56,642,665 (GRCm39) |
F169L |
probably benign |
Het |
Trp53rkb |
T |
A |
2: 166,637,743 (GRCm39) |
V233E |
probably damaging |
Het |
Ttc7b |
C |
T |
12: 100,381,389 (GRCm39) |
|
probably null |
Het |
Tubgcp3 |
A |
T |
8: 12,671,932 (GRCm39) |
L770* |
probably null |
Het |
Tut1 |
G |
A |
19: 8,943,466 (GRCm39) |
G851D |
probably benign |
Het |
Ubr1 |
G |
A |
2: 120,761,449 (GRCm39) |
T576I |
probably benign |
Het |
Vmn1r125 |
T |
A |
7: 21,006,530 (GRCm39) |
Y143N |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,839 (GRCm39) |
I317F |
probably benign |
Het |
Vmn2r95 |
T |
A |
17: 18,644,575 (GRCm39) |
N70K |
probably benign |
Het |
Vps35l |
A |
G |
7: 118,432,971 (GRCm39) |
N568S |
probably damaging |
Het |
Wdr59 |
A |
T |
8: 112,213,582 (GRCm39) |
L311* |
probably null |
Het |
Wnt2 |
A |
G |
6: 18,030,252 (GRCm39) |
L12P |
unknown |
Het |
Xrn1 |
T |
C |
9: 95,881,550 (GRCm39) |
I700T |
probably benign |
Het |
Ypel1 |
A |
G |
16: 16,900,443 (GRCm39) |
H98R |
probably benign |
Het |
Zfp219 |
T |
C |
14: 52,245,691 (GRCm39) |
T434A |
probably benign |
Het |
Zik1 |
A |
C |
7: 10,223,943 (GRCm39) |
C385G |
probably damaging |
Het |
|
Other mutations in Adam7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00667:Adam7
|
APN |
14 |
68,759,387 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01418:Adam7
|
APN |
14 |
68,762,655 (GRCm39) |
missense |
probably benign |
|
IGL01934:Adam7
|
APN |
14 |
68,770,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02655:Adam7
|
APN |
14 |
68,754,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Adam7
|
APN |
14 |
68,745,343 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4445001:Adam7
|
UTSW |
14 |
68,747,197 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0195:Adam7
|
UTSW |
14 |
68,765,076 (GRCm39) |
splice site |
probably benign |
|
R0277:Adam7
|
UTSW |
14 |
68,748,306 (GRCm39) |
splice site |
probably null |
|
R0362:Adam7
|
UTSW |
14 |
68,747,105 (GRCm39) |
splice site |
probably benign |
|
R0440:Adam7
|
UTSW |
14 |
68,748,305 (GRCm39) |
splice site |
probably null |
|
R0927:Adam7
|
UTSW |
14 |
68,754,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Adam7
|
UTSW |
14 |
68,752,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1270:Adam7
|
UTSW |
14 |
68,765,118 (GRCm39) |
missense |
probably damaging |
0.98 |
R1299:Adam7
|
UTSW |
14 |
68,763,748 (GRCm39) |
splice site |
probably benign |
|
R1527:Adam7
|
UTSW |
14 |
68,738,970 (GRCm39) |
missense |
probably benign |
0.04 |
R1543:Adam7
|
UTSW |
14 |
68,759,371 (GRCm39) |
splice site |
probably benign |
|
R1731:Adam7
|
UTSW |
14 |
68,762,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Adam7
|
UTSW |
14 |
68,735,899 (GRCm39) |
missense |
probably benign |
0.00 |
R2062:Adam7
|
UTSW |
14 |
68,742,610 (GRCm39) |
missense |
probably benign |
0.09 |
R2156:Adam7
|
UTSW |
14 |
68,748,792 (GRCm39) |
missense |
probably benign |
0.02 |
R2353:Adam7
|
UTSW |
14 |
68,742,537 (GRCm39) |
missense |
probably benign |
0.01 |
R2697:Adam7
|
UTSW |
14 |
68,752,232 (GRCm39) |
nonsense |
probably null |
|
R4080:Adam7
|
UTSW |
14 |
68,757,988 (GRCm39) |
missense |
probably benign |
0.05 |
R4775:Adam7
|
UTSW |
14 |
68,745,361 (GRCm39) |
missense |
probably benign |
0.41 |
R5202:Adam7
|
UTSW |
14 |
68,745,305 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6006:Adam7
|
UTSW |
14 |
68,748,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6087:Adam7
|
UTSW |
14 |
68,748,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Adam7
|
UTSW |
14 |
68,742,546 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6417:Adam7
|
UTSW |
14 |
68,742,070 (GRCm39) |
missense |
probably benign |
0.37 |
R6672:Adam7
|
UTSW |
14 |
68,742,151 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6756:Adam7
|
UTSW |
14 |
68,762,728 (GRCm39) |
missense |
probably benign |
0.00 |
R6777:Adam7
|
UTSW |
14 |
68,762,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Adam7
|
UTSW |
14 |
68,771,100 (GRCm39) |
missense |
probably benign |
0.22 |
R7127:Adam7
|
UTSW |
14 |
68,752,218 (GRCm39) |
critical splice donor site |
probably null |
|
R7209:Adam7
|
UTSW |
14 |
68,767,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Adam7
|
UTSW |
14 |
68,741,915 (GRCm39) |
splice site |
probably null |
|
R7675:Adam7
|
UTSW |
14 |
68,737,302 (GRCm39) |
missense |
probably benign |
0.07 |
R7788:Adam7
|
UTSW |
14 |
68,750,094 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7868:Adam7
|
UTSW |
14 |
68,770,090 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8135:Adam7
|
UTSW |
14 |
68,754,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Adam7
|
UTSW |
14 |
68,745,334 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8507:Adam7
|
UTSW |
14 |
68,763,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9049:Adam7
|
UTSW |
14 |
68,762,674 (GRCm39) |
missense |
probably benign |
0.01 |
R9240:Adam7
|
UTSW |
14 |
68,747,208 (GRCm39) |
missense |
probably benign |
0.02 |
R9429:Adam7
|
UTSW |
14 |
68,771,080 (GRCm39) |
missense |
probably null |
|
R9744:Adam7
|
UTSW |
14 |
68,742,583 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Adam7
|
UTSW |
14 |
68,765,150 (GRCm39) |
missense |
probably benign |
0.26 |
|