Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actrt3 |
A |
G |
3: 30,653,847 (GRCm39) |
V51A |
probably damaging |
Het |
Adgb |
C |
T |
10: 10,307,025 (GRCm39) |
|
probably null |
Het |
Als2 |
A |
G |
1: 59,250,296 (GRCm39) |
S483P |
probably damaging |
Het |
Ankrd10 |
C |
T |
8: 11,665,682 (GRCm39) |
R306H |
probably damaging |
Het |
Arhgef10 |
T |
C |
8: 15,025,093 (GRCm39) |
|
probably null |
Het |
Arhgef10 |
A |
G |
8: 15,025,666 (GRCm39) |
I459V |
probably benign |
Het |
Armc2 |
C |
T |
10: 41,842,696 (GRCm39) |
|
probably null |
Het |
Atp12a |
A |
G |
14: 56,624,407 (GRCm39) |
R952G |
possibly damaging |
Het |
Atp6v1g1 |
A |
G |
4: 63,468,258 (GRCm39) |
Y87C |
probably benign |
Het |
Cacna2d1 |
G |
A |
5: 16,517,566 (GRCm39) |
C404Y |
probably damaging |
Het |
Ccdc59 |
A |
T |
10: 105,677,388 (GRCm39) |
K9M |
possibly damaging |
Het |
Cd6 |
A |
G |
19: 10,771,990 (GRCm39) |
I307T |
possibly damaging |
Het |
Cimap1d |
G |
A |
10: 79,481,487 (GRCm39) |
T14I |
probably benign |
Het |
Clasrp |
C |
A |
7: 19,319,165 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
T |
C |
4: 128,451,511 (GRCm39) |
F113S |
unknown |
Het |
Csmd3 |
C |
T |
15: 47,721,320 (GRCm39) |
G1437D |
probably damaging |
Het |
Cyp4a14 |
C |
A |
4: 115,344,498 (GRCm39) |
G456W |
probably damaging |
Het |
Cyp4a30b |
A |
G |
4: 115,315,559 (GRCm39) |
H260R |
possibly damaging |
Het |
Dcp1b |
C |
T |
6: 119,191,735 (GRCm39) |
S217L |
probably benign |
Het |
Dennd2b |
A |
T |
7: 109,156,637 (GRCm39) |
Y38N |
probably benign |
Het |
Dhx57 |
A |
T |
17: 80,558,805 (GRCm39) |
D1051E |
probably benign |
Het |
Dmp1 |
A |
G |
5: 104,359,974 (GRCm39) |
S217G |
probably benign |
Het |
Eef2 |
GCCC |
GCCCC |
10: 81,014,601 (GRCm39) |
|
probably null |
Het |
Eif4enif1 |
C |
T |
11: 3,192,586 (GRCm39) |
P805S |
probably damaging |
Het |
Eral1 |
A |
G |
11: 77,967,104 (GRCm39) |
I164T |
possibly damaging |
Het |
Esr1 |
G |
A |
10: 4,947,890 (GRCm39) |
R481H |
probably damaging |
Het |
Fan1 |
A |
G |
7: 64,012,938 (GRCm39) |
I668T |
probably benign |
Het |
Gbp11 |
C |
T |
5: 105,478,866 (GRCm39) |
D191N |
probably benign |
Het |
Gria2 |
G |
A |
3: 80,609,799 (GRCm39) |
T670I |
probably damaging |
Het |
Gria4 |
T |
A |
9: 4,503,614 (GRCm39) |
N334I |
probably damaging |
Het |
Grm5 |
T |
C |
7: 87,251,930 (GRCm39) |
V60A |
possibly damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Ift172 |
C |
T |
5: 31,415,205 (GRCm39) |
V1335I |
probably benign |
Het |
Ino80d |
C |
T |
1: 63,100,198 (GRCm39) |
|
probably null |
Het |
Kif1c |
A |
G |
11: 70,614,907 (GRCm39) |
E567G |
probably damaging |
Het |
Krt31 |
T |
G |
11: 99,938,699 (GRCm39) |
N298T |
possibly damaging |
Het |
Matr3 |
T |
A |
18: 35,705,349 (GRCm39) |
S91R |
probably benign |
Het |
Mdm1 |
A |
G |
10: 117,986,847 (GRCm39) |
T267A |
probably benign |
Het |
Mlxip |
A |
G |
5: 123,590,730 (GRCm39) |
M878V |
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,386,875 (GRCm39) |
|
silent |
Het |
Mroh2a |
GCCC |
GC |
1: 88,159,979 (GRCm39) |
|
probably null |
Het |
Mtor |
T |
A |
4: 148,624,487 (GRCm39) |
M2089K |
probably benign |
Het |
Mylk2 |
A |
G |
2: 152,761,268 (GRCm39) |
K457R |
probably damaging |
Het |
Nomo1 |
C |
A |
7: 45,696,361 (GRCm39) |
T293N |
probably damaging |
Het |
Or10g1 |
T |
G |
14: 52,648,318 (GRCm39) |
T4P |
probably benign |
Het |
Or6c211 |
A |
T |
10: 129,505,628 (GRCm39) |
C253* |
probably null |
Het |
Or8k33 |
T |
C |
2: 86,383,928 (GRCm39) |
D180G |
possibly damaging |
Het |
Ostc |
T |
C |
3: 130,497,157 (GRCm39) |
N80S |
probably damaging |
Het |
Otud4 |
T |
A |
8: 80,387,702 (GRCm39) |
N300K |
possibly damaging |
Het |
Palmd |
T |
C |
3: 116,717,400 (GRCm39) |
R366G |
possibly damaging |
Het |
Pcdhb20 |
A |
T |
18: 37,638,833 (GRCm39) |
Q453L |
possibly damaging |
Het |
Pcdhga9 |
T |
A |
18: 37,870,524 (GRCm39) |
Y118N |
possibly damaging |
Het |
Pes1 |
C |
A |
11: 3,926,834 (GRCm39) |
T372K |
probably benign |
Het |
Plcl1 |
A |
T |
1: 55,736,309 (GRCm39) |
D550V |
probably benign |
Het |
Plekhg5 |
T |
A |
4: 152,191,960 (GRCm39) |
C433S |
probably benign |
Het |
Plin2 |
A |
G |
4: 86,586,915 (GRCm39) |
M1T |
probably null |
Het |
Ppp1r7 |
T |
A |
1: 93,285,585 (GRCm39) |
|
probably null |
Het |
Psmb8 |
T |
C |
17: 34,419,144 (GRCm39) |
I146T |
probably damaging |
Het |
Pzp |
A |
T |
6: 128,462,519 (GRCm39) |
|
probably null |
Het |
Reln |
C |
T |
5: 22,254,789 (GRCm39) |
V527I |
possibly damaging |
Het |
Retnla |
A |
G |
16: 48,663,975 (GRCm39) |
R90G |
probably benign |
Het |
Semp2l2b |
A |
T |
10: 21,943,278 (GRCm39) |
I234N |
probably benign |
Het |
Shoc1 |
A |
C |
4: 59,093,850 (GRCm39) |
L226R |
probably damaging |
Het |
Slc39a8 |
T |
A |
3: 135,592,554 (GRCm39) |
|
probably null |
Het |
Slc5a8 |
A |
G |
10: 88,740,825 (GRCm39) |
I247V |
probably benign |
Het |
Spcs2 |
T |
C |
7: 99,488,968 (GRCm39) |
D240G |
probably damaging |
Het |
Stx3 |
A |
T |
19: 11,766,938 (GRCm39) |
V91D |
probably damaging |
Het |
Tafa2 |
A |
T |
10: 123,540,270 (GRCm39) |
H42L |
possibly damaging |
Het |
Tbc1d8 |
A |
G |
1: 39,444,398 (GRCm39) |
F187S |
probably damaging |
Het |
Thbs1 |
C |
G |
2: 117,949,859 (GRCm39) |
N611K |
probably damaging |
Het |
Tipin |
A |
C |
9: 64,211,609 (GRCm39) |
S232R |
probably benign |
Het |
Tmem132b |
A |
G |
5: 125,715,332 (GRCm39) |
D347G |
probably benign |
Het |
Vmn2r68 |
A |
C |
7: 84,882,834 (GRCm39) |
M306R |
probably benign |
Het |
Vwa7 |
G |
A |
17: 35,240,218 (GRCm39) |
M395I |
probably damaging |
Het |
Ybx3 |
G |
A |
6: 131,347,376 (GRCm39) |
A253V |
probably damaging |
Het |
Zfp53 |
A |
T |
17: 21,728,340 (GRCm39) |
E124D |
probably benign |
Het |
|
Other mutations in Rel |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00663:Rel
|
APN |
11 |
23,707,043 (GRCm39) |
missense |
probably benign |
0.31 |
IGL00819:Rel
|
APN |
11 |
23,693,029 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00906:Rel
|
APN |
11 |
23,694,266 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01358:Rel
|
APN |
11 |
23,711,155 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01820:Rel
|
APN |
11 |
23,703,218 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01889:Rel
|
APN |
11 |
23,707,035 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03270:Rel
|
APN |
11 |
23,692,584 (GRCm39) |
missense |
probably benign |
0.16 |
Amun-ra
|
UTSW |
11 |
23,707,026 (GRCm39) |
nonsense |
probably null |
|
Fleur
|
UTSW |
11 |
0 () |
unclassified |
|
|
giza
|
UTSW |
11 |
23,707,010 (GRCm39) |
missense |
probably damaging |
1.00 |
Horus
|
UTSW |
11 |
23,703,215 (GRCm39) |
critical splice donor site |
probably null |
|
osirus
|
UTSW |
11 |
23,692,713 (GRCm39) |
missense |
probably benign |
0.00 |
Seth
|
UTSW |
11 |
23,698,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Rel
|
UTSW |
11 |
23,707,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Rel
|
UTSW |
11 |
23,692,439 (GRCm39) |
missense |
probably benign |
0.02 |
R0930:Rel
|
UTSW |
11 |
23,692,439 (GRCm39) |
missense |
probably benign |
0.02 |
R1312:Rel
|
UTSW |
11 |
23,707,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1339:Rel
|
UTSW |
11 |
23,695,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Rel
|
UTSW |
11 |
23,695,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Rel
|
UTSW |
11 |
23,692,761 (GRCm39) |
missense |
probably benign |
|
R1981:Rel
|
UTSW |
11 |
23,692,761 (GRCm39) |
missense |
probably benign |
|
R1982:Rel
|
UTSW |
11 |
23,692,761 (GRCm39) |
missense |
probably benign |
|
R2513:Rel
|
UTSW |
11 |
23,695,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Rel
|
UTSW |
11 |
23,711,129 (GRCm39) |
missense |
probably benign |
|
R2871:Rel
|
UTSW |
11 |
23,711,129 (GRCm39) |
missense |
probably benign |
|
R2871:Rel
|
UTSW |
11 |
23,711,129 (GRCm39) |
missense |
probably benign |
|
R2872:Rel
|
UTSW |
11 |
23,711,129 (GRCm39) |
missense |
probably benign |
|
R2872:Rel
|
UTSW |
11 |
23,711,129 (GRCm39) |
missense |
probably benign |
|
R3617:Rel
|
UTSW |
11 |
23,695,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R3976:Rel
|
UTSW |
11 |
23,692,939 (GRCm39) |
missense |
probably benign |
0.07 |
R4010:Rel
|
UTSW |
11 |
23,711,138 (GRCm39) |
missense |
probably benign |
|
R4067:Rel
|
UTSW |
11 |
23,703,215 (GRCm39) |
critical splice donor site |
probably null |
|
R5345:Rel
|
UTSW |
11 |
23,692,462 (GRCm39) |
missense |
probably benign |
0.00 |
R5866:Rel
|
UTSW |
11 |
23,692,724 (GRCm39) |
nonsense |
probably null |
|
R6032:Rel
|
UTSW |
11 |
23,692,684 (GRCm39) |
missense |
probably benign |
0.02 |
R6032:Rel
|
UTSW |
11 |
23,692,684 (GRCm39) |
missense |
probably benign |
0.02 |
R6562:Rel
|
UTSW |
11 |
23,707,026 (GRCm39) |
nonsense |
probably null |
|
R6886:Rel
|
UTSW |
11 |
23,694,304 (GRCm39) |
missense |
probably benign |
0.03 |
R7516:Rel
|
UTSW |
11 |
23,692,785 (GRCm39) |
missense |
probably benign |
0.00 |
R7522:Rel
|
UTSW |
11 |
23,720,676 (GRCm39) |
splice site |
probably null |
|
R7663:Rel
|
UTSW |
11 |
23,692,713 (GRCm39) |
missense |
probably benign |
0.00 |
R7873:Rel
|
UTSW |
11 |
23,692,957 (GRCm39) |
missense |
probably benign |
0.00 |
R7960:Rel
|
UTSW |
11 |
23,694,493 (GRCm39) |
missense |
probably damaging |
0.98 |
R8679:Rel
|
UTSW |
11 |
23,692,430 (GRCm39) |
missense |
probably benign |
|
R8819:Rel
|
UTSW |
11 |
23,695,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Rel
|
UTSW |
11 |
23,698,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Rel
|
UTSW |
11 |
23,698,870 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Rel
|
UTSW |
11 |
23,695,472 (GRCm39) |
missense |
probably damaging |
0.99 |
|