Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
C |
5: 124,218,119 (GRCm39) |
M406V |
probably benign |
Het |
Adar |
T |
C |
3: 89,638,121 (GRCm39) |
S2P |
probably benign |
Het |
Adgre1 |
T |
A |
17: 57,750,939 (GRCm39) |
S538T |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,618,363 (GRCm39) |
I2803N |
possibly damaging |
Het |
Arid1b |
G |
A |
17: 5,393,207 (GRCm39) |
A2246T |
probably damaging |
Het |
BC024139 |
T |
C |
15: 76,005,947 (GRCm39) |
E418G |
probably damaging |
Het |
Bok |
A |
G |
1: 93,614,239 (GRCm39) |
D24G |
probably damaging |
Het |
Cabp2 |
T |
C |
19: 4,134,913 (GRCm39) |
|
probably benign |
Het |
Ccdc141 |
C |
A |
2: 76,995,582 (GRCm39) |
|
probably benign |
Het |
Ccdc178 |
T |
C |
18: 22,283,492 (GRCm39) |
T13A |
probably benign |
Het |
Ccdc42 |
G |
T |
11: 68,478,476 (GRCm39) |
V33F |
possibly damaging |
Het |
Clcn7 |
G |
A |
17: 25,368,176 (GRCm39) |
|
probably benign |
Het |
Cluh |
A |
G |
11: 74,548,176 (GRCm39) |
|
probably benign |
Het |
Cr1l |
A |
T |
1: 194,797,164 (GRCm39) |
|
probably benign |
Het |
Cracdl |
A |
G |
1: 37,663,720 (GRCm39) |
V726A |
probably benign |
Het |
Csnk1g3 |
T |
A |
18: 54,051,861 (GRCm39) |
|
probably benign |
Het |
Depdc5 |
T |
C |
5: 33,091,281 (GRCm39) |
|
probably benign |
Het |
Dgkh |
A |
C |
14: 78,807,569 (GRCm39) |
Y1149* |
probably null |
Het |
Dipk2a |
G |
T |
9: 94,406,533 (GRCm39) |
D291E |
probably benign |
Het |
Dnai1 |
A |
G |
4: 41,635,162 (GRCm39) |
|
probably benign |
Het |
Dync2i1 |
A |
G |
12: 116,196,256 (GRCm39) |
V497A |
probably benign |
Het |
Efcab2 |
A |
G |
1: 178,302,451 (GRCm39) |
E65G |
possibly damaging |
Het |
Eif4a3l1 |
A |
T |
6: 136,305,842 (GRCm39) |
D101V |
probably damaging |
Het |
Eno1b |
T |
C |
18: 48,180,806 (GRCm39) |
I328T |
probably benign |
Het |
Fgfr4 |
A |
G |
13: 55,309,198 (GRCm39) |
|
probably benign |
Het |
Garin5b |
A |
T |
7: 4,773,286 (GRCm39) |
L177Q |
probably damaging |
Het |
Gm10720 |
A |
C |
9: 3,015,787 (GRCm39) |
S44R |
probably null |
Het |
Gm17535 |
T |
A |
9: 3,035,786 (GRCm39) |
L218H |
probably benign |
Het |
Gm6471 |
A |
T |
7: 142,385,368 (GRCm39) |
|
noncoding transcript |
Het |
Hnrnpm |
C |
T |
17: 33,865,489 (GRCm39) |
R724Q |
probably damaging |
Het |
Homer1 |
C |
T |
13: 93,528,254 (GRCm39) |
T117I |
possibly damaging |
Het |
Hoxd4 |
A |
T |
2: 74,557,801 (GRCm39) |
Q60L |
probably damaging |
Het |
Ift172 |
T |
C |
5: 31,417,968 (GRCm39) |
R1274G |
probably benign |
Het |
Ino80d |
A |
G |
1: 63,097,477 (GRCm39) |
S806P |
probably damaging |
Het |
Itga10 |
T |
C |
3: 96,561,016 (GRCm39) |
V627A |
probably benign |
Het |
Itgb2l |
A |
G |
16: 96,238,569 (GRCm39) |
Y77H |
possibly damaging |
Het |
Kel |
A |
T |
6: 41,678,877 (GRCm39) |
H195Q |
probably benign |
Het |
Klhdc7a |
A |
G |
4: 139,694,582 (GRCm39) |
S122P |
possibly damaging |
Het |
Krt71 |
T |
A |
15: 101,643,141 (GRCm39) |
I456F |
possibly damaging |
Het |
Lats1 |
T |
A |
10: 7,567,339 (GRCm39) |
S37T |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,013,031 (GRCm39) |
H1858L |
possibly damaging |
Het |
Matk |
A |
T |
10: 81,098,676 (GRCm39) |
T461S |
probably benign |
Het |
Meikin |
A |
G |
11: 54,300,468 (GRCm39) |
|
probably benign |
Het |
Muc6 |
T |
C |
7: 141,214,029 (GRCm39) |
Q2832R |
possibly damaging |
Het |
Myo10 |
T |
C |
15: 25,781,324 (GRCm39) |
F194L |
possibly damaging |
Het |
Nbas |
G |
A |
12: 13,323,877 (GRCm39) |
|
probably benign |
Het |
Nme4 |
A |
G |
17: 26,312,831 (GRCm39) |
|
probably null |
Het |
Or13p8 |
A |
T |
4: 118,583,530 (GRCm39) |
I29F |
possibly damaging |
Het |
Or4c112 |
T |
A |
2: 88,853,540 (GRCm39) |
N269I |
probably benign |
Het |
Or5w13 |
A |
G |
2: 87,523,948 (GRCm39) |
S93P |
probably benign |
Het |
Or7g32 |
T |
A |
9: 19,408,233 (GRCm39) |
L63H |
probably damaging |
Het |
Or8g34 |
T |
C |
9: 39,372,967 (GRCm39) |
V80A |
probably damaging |
Het |
Pacsin2 |
T |
C |
15: 83,261,862 (GRCm39) |
Q473R |
probably benign |
Het |
Patz1 |
A |
G |
11: 3,243,288 (GRCm39) |
H427R |
probably damaging |
Het |
Pkp3 |
A |
G |
7: 140,663,256 (GRCm39) |
Y367C |
probably damaging |
Het |
Prdm2 |
G |
A |
4: 142,860,338 (GRCm39) |
P984L |
possibly damaging |
Het |
Rev3l |
T |
A |
10: 39,750,124 (GRCm39) |
C3091* |
probably null |
Het |
Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
Rpl5 |
T |
C |
5: 108,052,623 (GRCm39) |
F140L |
probably benign |
Het |
Sec24a |
A |
C |
11: 51,591,653 (GRCm39) |
I1014M |
probably benign |
Het |
Serpinb11 |
A |
G |
1: 107,299,933 (GRCm39) |
H93R |
probably benign |
Het |
Shank2 |
C |
A |
7: 143,623,872 (GRCm39) |
H286N |
probably benign |
Het |
Sipa1l2 |
G |
T |
8: 126,148,637 (GRCm39) |
Q1651K |
probably damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,963,002 (GRCm39) |
F75L |
possibly damaging |
Het |
Slco1a1 |
G |
T |
6: 141,856,427 (GRCm39) |
|
probably benign |
Het |
Smg5 |
C |
T |
3: 88,261,179 (GRCm39) |
|
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Taf8 |
A |
T |
17: 47,809,177 (GRCm39) |
|
probably benign |
Het |
Tars3 |
A |
G |
7: 65,333,829 (GRCm39) |
D617G |
probably damaging |
Het |
Tbc1d5 |
A |
T |
17: 51,291,715 (GRCm39) |
|
probably benign |
Het |
Tfcp2 |
C |
G |
15: 100,412,708 (GRCm39) |
E315Q |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,147,345 (GRCm39) |
S540R |
probably damaging |
Het |
Tmprss4 |
T |
C |
9: 45,095,634 (GRCm39) |
Q70R |
probably benign |
Het |
Trip13 |
G |
T |
13: 74,068,183 (GRCm39) |
A266E |
possibly damaging |
Het |
Ttc24 |
T |
A |
3: 87,982,234 (GRCm39) |
|
probably benign |
Het |
Ttll5 |
T |
A |
12: 85,878,740 (GRCm39) |
I49N |
probably damaging |
Het |
Tut7 |
G |
A |
13: 59,930,150 (GRCm39) |
R962* |
probably null |
Het |
Ube2ql1 |
A |
T |
13: 69,886,711 (GRCm39) |
M250K |
possibly damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,866,211 (GRCm39) |
D25E |
probably damaging |
Het |
Vmn2r84 |
A |
G |
10: 130,227,877 (GRCm39) |
Y120H |
probably benign |
Het |
Wdr6 |
G |
A |
9: 108,452,441 (GRCm39) |
R481C |
probably damaging |
Het |
Zdhhc17 |
A |
T |
10: 110,790,955 (GRCm39) |
Y371* |
probably null |
Het |
Zfp292 |
T |
C |
4: 34,811,185 (GRCm39) |
N620D |
probably benign |
Het |
Zfp932 |
T |
A |
5: 110,154,834 (GRCm39) |
Y11N |
probably benign |
Het |
|
Other mutations in Amn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02391:Amn1
|
APN |
6 |
149,070,944 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4453001:Amn1
|
UTSW |
6 |
149,072,357 (GRCm39) |
missense |
probably benign |
0.00 |
R0494:Amn1
|
UTSW |
6 |
149,086,634 (GRCm39) |
unclassified |
probably benign |
|
R0557:Amn1
|
UTSW |
6 |
149,072,503 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0717:Amn1
|
UTSW |
6 |
149,084,970 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0736:Amn1
|
UTSW |
6 |
149,084,970 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3420:Amn1
|
UTSW |
6 |
149,070,950 (GRCm39) |
nonsense |
probably null |
|
R3421:Amn1
|
UTSW |
6 |
149,070,950 (GRCm39) |
nonsense |
probably null |
|
R4466:Amn1
|
UTSW |
6 |
149,068,343 (GRCm39) |
splice site |
probably null |
|
R4760:Amn1
|
UTSW |
6 |
149,086,611 (GRCm39) |
missense |
probably benign |
|
R5294:Amn1
|
UTSW |
6 |
149,086,622 (GRCm39) |
unclassified |
probably benign |
|
R5356:Amn1
|
UTSW |
6 |
149,068,392 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5561:Amn1
|
UTSW |
6 |
149,086,522 (GRCm39) |
missense |
probably damaging |
0.98 |
R7501:Amn1
|
UTSW |
6 |
149,086,529 (GRCm39) |
missense |
probably benign |
0.19 |
R7564:Amn1
|
UTSW |
6 |
149,086,529 (GRCm39) |
missense |
probably benign |
0.19 |
R7643:Amn1
|
UTSW |
6 |
149,086,529 (GRCm39) |
missense |
probably benign |
0.19 |
R7645:Amn1
|
UTSW |
6 |
149,086,529 (GRCm39) |
missense |
probably benign |
0.19 |
R8097:Amn1
|
UTSW |
6 |
149,070,853 (GRCm39) |
unclassified |
probably benign |
|
R9390:Amn1
|
UTSW |
6 |
149,084,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Amn1
|
UTSW |
6 |
149,090,103 (GRCm39) |
start gained |
probably benign |
|
X0064:Amn1
|
UTSW |
6 |
149,072,533 (GRCm39) |
missense |
probably damaging |
1.00 |
|