Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
G |
A |
14: 54,822,444 (GRCm39) |
R8* |
probably null |
Het |
Abhd17a |
A |
G |
10: 80,421,440 (GRCm39) |
|
probably null |
Het |
Acsm1 |
A |
G |
7: 119,255,262 (GRCm39) |
R415G |
probably damaging |
Het |
Acta1 |
G |
T |
8: 124,618,803 (GRCm39) |
T360N |
probably benign |
Het |
Adgrd1 |
G |
T |
5: 129,192,159 (GRCm39) |
K76N |
probably benign |
Het |
Afdn |
A |
G |
17: 14,030,695 (GRCm39) |
E202G |
probably damaging |
Het |
Agps |
T |
A |
2: 75,689,270 (GRCm39) |
M156K |
probably benign |
Het |
Agxt |
A |
G |
1: 93,065,037 (GRCm39) |
I149V |
probably benign |
Het |
Aoc1l1 |
T |
A |
6: 48,954,689 (GRCm39) |
L609* |
probably null |
Het |
Aqp2 |
A |
G |
15: 99,477,247 (GRCm39) |
T72A |
probably damaging |
Het |
Arhgap18 |
T |
A |
10: 26,725,938 (GRCm39) |
D54E |
probably benign |
Het |
Asb8 |
C |
A |
15: 98,033,950 (GRCm39) |
E202* |
probably null |
Het |
Bmp5 |
A |
G |
9: 75,801,072 (GRCm39) |
I401V |
probably damaging |
Het |
Bscl2 |
T |
C |
19: 8,822,684 (GRCm39) |
|
probably null |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cep112 |
A |
G |
11: 108,497,151 (GRCm39) |
E697G |
probably damaging |
Het |
Cerk |
G |
A |
15: 86,027,009 (GRCm39) |
S167L |
probably benign |
Het |
Chrm3 |
T |
A |
13: 9,928,371 (GRCm39) |
I222F |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Cntrl |
CAGAG |
CAG |
2: 35,012,818 (GRCm39) |
|
probably null |
Het |
Commd10 |
A |
T |
18: 47,096,814 (GRCm39) |
T74S |
probably benign |
Het |
Cyp4f39 |
T |
C |
17: 32,701,112 (GRCm39) |
F201L |
probably benign |
Het |
Dennd4a |
A |
G |
9: 64,796,887 (GRCm39) |
T860A |
possibly damaging |
Het |
Dlg5 |
A |
T |
14: 24,204,715 (GRCm39) |
I1253N |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,307,830 (GRCm39) |
M3048K |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,935,509 (GRCm39) |
M1970T |
probably damaging |
Het |
Dsc3 |
A |
T |
18: 20,122,737 (GRCm39) |
D62E |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dusp7 |
C |
T |
9: 106,251,096 (GRCm39) |
T407M |
probably damaging |
Het |
Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
Eif1ad8 |
A |
G |
12: 87,564,046 (GRCm39) |
D127G |
unknown |
Het |
Entpd5 |
A |
G |
12: 84,443,632 (GRCm39) |
I12T |
probably benign |
Het |
Espn |
T |
C |
4: 152,205,714 (GRCm39) |
E408G |
probably damaging |
Het |
Fhip1b |
A |
T |
7: 105,039,046 (GRCm39) |
D64E |
probably damaging |
Het |
Gdpd3 |
A |
G |
7: 126,367,766 (GRCm39) |
T200A |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
Gm5134 |
G |
A |
10: 75,840,718 (GRCm39) |
A521T |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
H2-M10.1 |
T |
C |
17: 36,636,108 (GRCm39) |
D153G |
possibly damaging |
Het |
Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
I0C0044D17Rik |
A |
G |
4: 98,708,533 (GRCm39) |
|
probably benign |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,898,376 (GRCm39) |
Q730L |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 66,993,777 (GRCm39) |
L86* |
probably null |
Het |
Kat5 |
T |
A |
19: 5,655,713 (GRCm39) |
|
probably null |
Het |
Kif14 |
A |
G |
1: 136,414,818 (GRCm39) |
N768S |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,437,905 (GRCm39) |
E1199G |
possibly damaging |
Het |
Klhl29 |
A |
G |
12: 5,187,876 (GRCm39) |
S163P |
probably damaging |
Het |
Kmt2c |
C |
A |
5: 25,490,077 (GRCm39) |
Q4287H |
probably damaging |
Het |
Krt82 |
T |
A |
15: 101,453,591 (GRCm39) |
Q265L |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,248,895 (GRCm39) |
C7210Y |
probably damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Myom2 |
T |
G |
8: 15,156,379 (GRCm39) |
I742S |
probably damaging |
Het |
Narf |
A |
T |
11: 121,141,195 (GRCm39) |
R310* |
probably null |
Het |
Nktr |
T |
A |
9: 121,570,760 (GRCm39) |
D167E |
probably damaging |
Het |
Nle1 |
A |
G |
11: 82,796,192 (GRCm39) |
W183R |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,108,871 (GRCm39) |
N425S |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4a27 |
A |
T |
2: 88,559,089 (GRCm39) |
Y285N |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4d5 |
T |
A |
9: 40,012,415 (GRCm39) |
I124L |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,748,036 (GRCm39) |
V37A |
probably benign |
Het |
Or8g52 |
A |
T |
9: 39,631,411 (GRCm39) |
D296V |
probably damaging |
Het |
Or8s2 |
G |
A |
15: 98,276,277 (GRCm39) |
T238I |
possibly damaging |
Het |
Otol1 |
T |
A |
3: 69,926,169 (GRCm39) |
F115I |
probably benign |
Het |
Parp8 |
T |
A |
13: 117,031,422 (GRCm39) |
D430V |
probably benign |
Het |
Pex7 |
T |
A |
10: 19,770,061 (GRCm39) |
H123L |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,410,909 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
G |
A |
15: 44,445,137 (GRCm39) |
D3670N |
probably damaging |
Het |
Plec |
T |
C |
15: 76,067,374 (GRCm39) |
T1331A |
probably benign |
Het |
Plekha4 |
A |
G |
7: 45,203,222 (GRCm39) |
D704G |
probably benign |
Het |
Plxnb2 |
T |
A |
15: 89,043,205 (GRCm39) |
N1453I |
probably damaging |
Het |
Pms1 |
T |
A |
1: 53,321,147 (GRCm39) |
I29F |
probably damaging |
Het |
Ppp1r1a |
G |
A |
15: 103,439,833 (GRCm39) |
T153I |
probably damaging |
Het |
Pramel12 |
T |
A |
4: 143,143,441 (GRCm39) |
L69Q |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptpre |
A |
G |
7: 135,272,424 (GRCm39) |
|
probably benign |
Het |
Ptprt |
A |
T |
2: 161,376,465 (GRCm39) |
I1312N |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rims1 |
C |
T |
1: 22,635,516 (GRCm39) |
C155Y |
probably damaging |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Slitrk6 |
T |
G |
14: 110,988,226 (GRCm39) |
T494P |
probably benign |
Het |
Sltm |
G |
A |
9: 70,488,583 (GRCm39) |
G578S |
probably benign |
Het |
Smyd5 |
A |
G |
6: 85,421,300 (GRCm39) |
E338G |
probably benign |
Het |
Snx2 |
G |
A |
18: 53,327,516 (GRCm39) |
V81M |
probably damaging |
Het |
Sp2 |
G |
T |
11: 96,852,191 (GRCm39) |
N244K |
probably benign |
Het |
Sspo |
C |
A |
6: 48,437,697 (GRCm39) |
|
probably benign |
Het |
Sspo |
A |
C |
6: 48,440,465 (GRCm39) |
D1568A |
probably benign |
Het |
Ssrp1 |
T |
C |
2: 84,871,771 (GRCm39) |
|
probably benign |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
Syt7 |
G |
A |
19: 10,416,577 (GRCm39) |
R138Q |
probably benign |
Het |
Taar7f |
T |
C |
10: 23,926,323 (GRCm39) |
Y306H |
possibly damaging |
Het |
Tbccd1 |
T |
C |
16: 22,637,291 (GRCm39) |
|
probably null |
Het |
Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
Tex261 |
A |
G |
6: 83,749,241 (GRCm39) |
Y119H |
probably damaging |
Het |
Tmem131l |
T |
G |
3: 83,850,095 (GRCm39) |
E234D |
probably damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Top6bl |
A |
G |
19: 4,748,633 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ubap1 |
C |
T |
4: 41,379,257 (GRCm39) |
A157V |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Uso1 |
G |
A |
5: 92,329,795 (GRCm39) |
G427R |
probably damaging |
Het |
Usp15 |
A |
T |
10: 122,955,042 (GRCm39) |
V912D |
probably damaging |
Het |
Vmn1r20 |
T |
C |
6: 57,408,943 (GRCm39) |
S90P |
probably damaging |
Het |
Vmn1r32 |
T |
C |
6: 66,530,545 (GRCm39) |
K77R |
probably damaging |
Het |
Vmn2r100 |
A |
G |
17: 19,742,312 (GRCm39) |
K229E |
probably benign |
Het |
Vmn2r106 |
A |
G |
17: 20,488,566 (GRCm39) |
V611A |
possibly damaging |
Het |
Xrcc6 |
T |
A |
15: 81,907,178 (GRCm39) |
F167I |
probably damaging |
Het |
Zbtb21 |
G |
T |
16: 97,751,355 (GRCm39) |
P804H |
probably damaging |
Het |
Zdhhc3 |
T |
C |
9: 122,929,602 (GRCm39) |
D11G |
probably damaging |
Het |
Zfhx3 |
A |
G |
8: 109,671,809 (GRCm39) |
T1324A |
probably benign |
Het |
Zfp281 |
GCGGCAGCTCCGGCAGC |
GCGGCAGCTCCGGCAGCTCCGGCAGC |
1: 136,553,091 (GRCm39) |
|
probably benign |
Het |
Zfp608 |
G |
T |
18: 55,028,637 (GRCm39) |
L1259I |
probably damaging |
Het |
|
Other mutations in Adam6a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Adam6a
|
APN |
12 |
113,508,845 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00896:Adam6a
|
APN |
12 |
113,509,030 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01146:Adam6a
|
APN |
12 |
113,507,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01285:Adam6a
|
APN |
12 |
113,509,893 (GRCm39) |
makesense |
probably null |
|
IGL01839:Adam6a
|
APN |
12 |
113,508,242 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01906:Adam6a
|
APN |
12 |
113,507,951 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02306:Adam6a
|
APN |
12 |
113,509,343 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03146:Adam6a
|
APN |
12 |
113,509,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03176:Adam6a
|
APN |
12 |
113,509,822 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03365:Adam6a
|
APN |
12 |
113,507,765 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03373:Adam6a
|
APN |
12 |
113,509,172 (GRCm39) |
missense |
possibly damaging |
0.55 |
PIT4802001:Adam6a
|
UTSW |
12 |
113,509,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R0091:Adam6a
|
UTSW |
12 |
113,507,849 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0149:Adam6a
|
UTSW |
12 |
113,509,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0348:Adam6a
|
UTSW |
12 |
113,508,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R0376:Adam6a
|
UTSW |
12 |
113,508,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Adam6a
|
UTSW |
12 |
113,508,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Adam6a
|
UTSW |
12 |
113,508,069 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1553:Adam6a
|
UTSW |
12 |
113,508,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R1679:Adam6a
|
UTSW |
12 |
113,508,376 (GRCm39) |
missense |
probably benign |
0.00 |
R1808:Adam6a
|
UTSW |
12 |
113,508,334 (GRCm39) |
missense |
probably benign |
0.00 |
R1826:Adam6a
|
UTSW |
12 |
113,509,742 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1856:Adam6a
|
UTSW |
12 |
113,508,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1916:Adam6a
|
UTSW |
12 |
113,509,556 (GRCm39) |
missense |
probably benign |
|
R2011:Adam6a
|
UTSW |
12 |
113,508,998 (GRCm39) |
missense |
probably benign |
0.09 |
R2364:Adam6a
|
UTSW |
12 |
113,508,250 (GRCm39) |
missense |
probably benign |
0.05 |
R3820:Adam6a
|
UTSW |
12 |
113,507,798 (GRCm39) |
missense |
probably benign |
0.00 |
R4119:Adam6a
|
UTSW |
12 |
113,508,194 (GRCm39) |
missense |
probably benign |
0.06 |
R4540:Adam6a
|
UTSW |
12 |
113,508,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Adam6a
|
UTSW |
12 |
113,508,569 (GRCm39) |
missense |
probably benign |
|
R4665:Adam6a
|
UTSW |
12 |
113,507,992 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4859:Adam6a
|
UTSW |
12 |
113,509,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R4997:Adam6a
|
UTSW |
12 |
113,508,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R5270:Adam6a
|
UTSW |
12 |
113,507,747 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5751:Adam6a
|
UTSW |
12 |
113,508,447 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5775:Adam6a
|
UTSW |
12 |
113,509,886 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5863:Adam6a
|
UTSW |
12 |
113,507,987 (GRCm39) |
missense |
probably benign |
0.01 |
R6154:Adam6a
|
UTSW |
12 |
113,509,292 (GRCm39) |
missense |
probably benign |
0.11 |
R6313:Adam6a
|
UTSW |
12 |
113,508,670 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6316:Adam6a
|
UTSW |
12 |
113,509,196 (GRCm39) |
missense |
probably benign |
0.27 |
R6706:Adam6a
|
UTSW |
12 |
113,508,886 (GRCm39) |
missense |
probably benign |
0.00 |
R6845:Adam6a
|
UTSW |
12 |
113,507,717 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7134:Adam6a
|
UTSW |
12 |
113,508,655 (GRCm39) |
missense |
probably benign |
0.04 |
R7179:Adam6a
|
UTSW |
12 |
113,509,291 (GRCm39) |
missense |
probably benign |
0.02 |
R7206:Adam6a
|
UTSW |
12 |
113,509,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:Adam6a
|
UTSW |
12 |
113,509,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Adam6a
|
UTSW |
12 |
113,509,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7676:Adam6a
|
UTSW |
12 |
113,508,196 (GRCm39) |
missense |
probably benign |
0.00 |
R7730:Adam6a
|
UTSW |
12 |
113,507,660 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7743:Adam6a
|
UTSW |
12 |
113,508,152 (GRCm39) |
missense |
probably benign |
|
R7841:Adam6a
|
UTSW |
12 |
113,509,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Adam6a
|
UTSW |
12 |
113,509,757 (GRCm39) |
missense |
probably benign |
0.08 |
R8531:Adam6a
|
UTSW |
12 |
113,508,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Adam6a
|
UTSW |
12 |
113,508,020 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9624:Adam6a
|
UTSW |
12 |
113,509,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R9679:Adam6a
|
UTSW |
12 |
113,509,542 (GRCm39) |
missense |
probably benign |
0.00 |
R9680:Adam6a
|
UTSW |
12 |
113,509,484 (GRCm39) |
nonsense |
probably null |
|
X0027:Adam6a
|
UTSW |
12 |
113,508,863 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Adam6a
|
UTSW |
12 |
113,508,941 (GRCm39) |
missense |
possibly damaging |
0.92 |
|